Yum, tasty mutations...

MutationT@ster 2025

NEVER press reload or F5 - unless you want to start from the very beginning.
Input seems to be ok - now mapping the variant to the different transcripts...
Querying Taster for transcript #1: ENST00000643088
Querying Taster for transcript #2: ENST00000643946
Querying Taster for transcript #3: ENST00000642206
Querying Taster for transcript #4: ENST00000382538
Querying Taster for transcript #5: ENST00000219476
Querying Taster for transcript #6: ENST00000645186
Querying Taster for transcript #7: ENST00000401874
Querying Taster for transcript #8: ENST00000644335
Querying Taster for transcript #9: ENST00000646388
Querying Taster for transcript #10: ENST00000439673
Querying Taster for transcript #11: ENST00000350773
Querying Taster for transcript #12: ENST00000642365
Querying Taster for transcript #13: ENST00000644329
Querying Taster for transcript #14: ENST00000642797
Querying Taster for transcript #15: ENST00000644043
Querying Taster for transcript #16: ENST00000642561
Querying Taster for transcript #17: ENST00000568454
Querying Taster for transcript #18: ENST00000642936
MT speed 2.05 s - this script 4.682548 s

Transcript summary:

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Yum, tasty mutations...

MutationT@ster 2025

Variant:

16:2084396C>T_1_ENST00000643088

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr16:2084396C>T (GRCh38)
Gene symbol TSC2
Gene constraints LOEUF: 0.18, LOF (oe): 0.13, misssense (oe): 0.98, synonymous (oe): 1.28 ? (gnomAD)
Ensembl transcript ID ENST00000643088.1
Genbank transcript ID
UniProt / AlphaMissense peptide N/A
Variant type Single base exchange
Gene region CDS
DNA changes c.3973C>T
g.36430C>T
AA changes Q1325* Score: 6.0?
Frameshift No
Length of protein NMD
Pathogenic variant (ClinVar)
Tuberous sclerosis syndrome
Tuberous sclerosis 2
See cases
pathogenicClinVar OMIM
Variant DBs
Not in dbSNP
Allele 'T' was not found in gnomAD
Protein conservation
SpeciesMatchGeneAAAlignment
Human      1325PLSKSSSSPELQTLQDILGDPGDK
mutated  no alignment    n/a
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
Protein features N/A
Phylogenetic conservation
PhyloPPhastCons
(flanking)-0.9380.04
5.7081
(flanking)6.7391
?
Splice sites No abrogation of potential splice sites predicted by MaxEntScan.
Distance from splice site N/A
Kozak consensus sequence altered? No
poly(A) signal N/A
AA sequence altered Yes
Chromosome 16
Strand 1
Original gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Original cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Wildtype AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKRIQTS LTSASLGSAD
ENSVAQADDS LKNLHLELTE TCLDMMARYV FSNFTAVPKR SPVGEFLLAG GRTKTWLVGN
KLVTVTTSVG TGTRSLLGLD SGELQSGPES SSSPGVHVRQ TKEAPAKLES QAGQQVSRGA
RDRVRSMSGG HGLRVGALDV PASQFLGSAT SPGPRTAPAA KPEKASAGTR VPVQEKTNLA
AYVPLLTQGW AEILVRRPTG NTSWLMSLEN PLSPFSSDIN NMPLQELSNA LMAAERFKEH
RDTALYKSLS VPAASTAKPP PLPRSNTDSA VVMEEGSPGE VPVLVEPPGL EDVEAALGMD
RRTDAYSRSS SVSSQEEKSL HAEELVGRGI PIERVVSSEG GRPSVDLSFQ PSQPLSKSSS
SPELQTLQDI LGDPGDKADV GRLSPEVKAR SQSGTLDGES AAWSASGEDS RGQPEGPLPS
SSPRSPSGLR PRGYTISDSA PSRRGKRVER DALKSRATAS NAEKVPGINP SFVFLQLYHS
PFFGDESNKP ILLPNESFER SVQLLDQIPS YDTHKIAVLY VGEGQSNSEL AILSNEHGSY
RYTEFLTGLG RLIELKDCQP DKVYLGGLDV CGEDGQFTYC WHDDIMQAVF HIATLMPTKD
VDKHRCDKKR HLGNDFVSIV YNDSGEDFKL GTIKGQFNFV HVIVTPLDYE CNLVSLQCRK
DMEGLVDTSV AKIVSDRNLP FVARQMALHA NMASQVHHSR SNPTDIYPSK WIARLRHIKR
LRQRICEEAA YSNPSLPLVH PPSHSKAPAQ TPAEPTPGYE VGQRKRLISS VEDFTEFV*
Mutated AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKRIQTS LTSASLGSAD
ENSVAQADDS LKNLHLELTE TCLDMMARYV FSNFTAVPKR SPVGEFLLAG GRTKTWLVGN
KLVTVTTSVG TGTRSLLGLD SGELQSGPES SSSPGVHVRQ TKEAPAKLES QAGQQVSRGA
RDRVRSMSGG HGLRVGALDV PASQFLGSAT SPGPRTAPAA KPEKASAGTR VPVQEKTNLA
AYVPLLTQGW AEILVRRPTG NTSWLMSLEN PLSPFSSDIN NMPLQELSNA LMAAERFKEH
RDTALYKSLS VPAASTAKPP PLPRSNTDSA VVMEEGSPGE VPVLVEPPGL EDVEAALGMD
RRTDAYSRSS SVSSQEEKSL HAEELVGRGI PIERVVSSEG GRPSVDLSFQ PSQPLSKSSS
SPEL*
Position of stopcodon in wt / mu CDS 5217 / 3975
Position (AA) of stopcodon in wt / mu AA sequence 1739 / 1325
Position of stopcodon in wt / mu cDNA 5335 / 4093
Position of start ATG in wt / mu cDNA 119 / 119
Last intron/exon boundary 5170
Theoretical NMD boundary in CDS 5001
Length of CDS 5217
Coding sequence (CDS) position 3973
cDNA position 4091
gDNA position 36430
Chromosomal position 2084396
Speed 0.12 s

All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project

Back to summary table

Yum, tasty mutations...

MutationT@ster 2025

Variant:

16:2084396C>T_2_ENST00000643946

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr16:2084396C>T (GRCh38)
Gene symbol TSC2
Gene constraints LOEUF: 0.18, LOF (oe): 0.13, misssense (oe): 0.99, synonymous (oe): 1.28 ? (gnomAD)
Ensembl transcript ID ENST00000643946.1
Genbank transcript ID
UniProt / AlphaMissense peptide N/A
Variant type Single base exchange
Gene region CDS
DNA changes c.4105C>T
g.36430C>T
AA changes Q1369* Score: 6.0?
Frameshift No
Length of protein NMD
Pathogenic variant (ClinVar)
Tuberous sclerosis syndrome
Tuberous sclerosis 2
See cases
pathogenicClinVar OMIM
Variant DBs
Not in dbSNP
Allele 'T' was not found in gnomAD
Protein conservation
SpeciesMatchGeneAAAlignment
Human      1369PLSKSSSSPELQTLQDILGDPGDK
mutated  no alignment    n/a
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
Protein features N/A
Phylogenetic conservation
PhyloPPhastCons
(flanking)-0.9380.04
5.7081
(flanking)6.7391
?
Splice sites No abrogation of potential splice sites predicted by MaxEntScan.
Distance from splice site N/A
Kozak consensus sequence altered? No
poly(A) signal N/A
AA sequence altered Yes
Chromosome 16
Strand 1
Original gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Original cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Wildtype AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSLRIA RPPKQGLNNS
PPVKEFKESS AAEAFRCRSI SVSEHVVRSR IQTSLTSASL GSADENSVAQ ADDSLKNLHL
ELTETCLDMM ARYVFSNFTA VPKRSPVGEF LLAGGRTKTW LVGNKLVTVT TSVGTGTRSL
LGLDSGELQS GPESSSSPGV HVRQTKEAPA KLESQAGQQV SRGARDRVRS MSGGHGLRVG
ALDVPASQFL GSATSPGPRT APAAKPEKAS AGTRVPVQEK TNLAAYVPLL TQGWAEILVR
RPTGNTSWLM SLENPLSPFS SDINNMPLQE LSNALMAAER FKEHRDTALY KSLSVPAAST
AKPPPLPRSN TDSAVVMEEG SPGEVPVLVE PPGLEDVEAA LGMDRRTDAY SRSSSVSSQE
EKSLHAEELV GRGIPIERVV SSEGGRPSVD LSFQPSQPLS KSSSSPELQT LQDILGDPGD
KADVGRLSPE VKARSQSGTL DGESAAWSAS GEDSRGQPEG PLPSSSPRSP SGLRPRGYTI
SDSAPSRRGK RVERDALKSR ATASNAEKVP GINPSFVFLQ LYHSPFFGDE SNKPILLPNE
SFERSVQLLD QIPSYDTHKI AVLYVGEGQS NSELAILSNE HGSYRYTEFL TGLGRLIELK
DCQPDKVYLG GLDVCGEDGQ FTYCWHDDIM QAVFHIATLM PTKDVDKHRC DKKRHLGNDF
VSIVYNDSGE DFKLGTIKGQ FNFVHVIVTP LDYECNLVSL QCRKDMEGLV DTSVAKIVSD
RNLPFVARQM ALHANMASQV HHSRSNPTDI YPSKWIARLR HIKRLRQRIC EEAAYSNPSL
PLVHPPSHSK APAQTPAEPT PGYEVGQRKR LISSVEDFTE FV*
Mutated AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSLRIA RPPKQGLNNS
PPVKEFKESS AAEAFRCRSI SVSEHVVRSR IQTSLTSASL GSADENSVAQ ADDSLKNLHL
ELTETCLDMM ARYVFSNFTA VPKRSPVGEF LLAGGRTKTW LVGNKLVTVT TSVGTGTRSL
LGLDSGELQS GPESSSSPGV HVRQTKEAPA KLESQAGQQV SRGARDRVRS MSGGHGLRVG
ALDVPASQFL GSATSPGPRT APAAKPEKAS AGTRVPVQEK TNLAAYVPLL TQGWAEILVR
RPTGNTSWLM SLENPLSPFS SDINNMPLQE LSNALMAAER FKEHRDTALY KSLSVPAAST
AKPPPLPRSN TDSAVVMEEG SPGEVPVLVE PPGLEDVEAA LGMDRRTDAY SRSSSVSSQE
EKSLHAEELV GRGIPIERVV SSEGGRPSVD LSFQPSQPLS KSSSSPEL*
Position of stopcodon in wt / mu CDS 5349 / 4107
Position (AA) of stopcodon in wt / mu AA sequence 1783 / 1369
Position of stopcodon in wt / mu cDNA 5467 / 4225
Position of start ATG in wt / mu cDNA 119 / 119
Last intron/exon boundary 5302
Theoretical NMD boundary in CDS 5133
Length of CDS 5349
Coding sequence (CDS) position 4105
cDNA position 4223
gDNA position 36430
Chromosomal position 2084396
Speed 0.11 s

All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project

Back to summary table

Yum, tasty mutations...

MutationT@ster 2025

Variant:

16:2084396C>T_3_ENST00000642206

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr16:2084396C>T (GRCh38)
Gene symbol TSC2
Gene constraints LOEUF: 1.24, LOF (oe): 0.59, misssense (oe): 1.05, synonymous (oe): 0.99 ? (gnomAD)
Ensembl transcript ID ENST00000642206.2
Genbank transcript ID NM_001406667 (by similarity), NM_001406668 (by similarity)
UniProt / AlphaMissense peptide N/A
Variant type Single base exchange
Gene region CDS
DNA changes c.4021C>T
g.36430C>T
AA changes Q1341* Score: 6.0?
Frameshift No
Length of protein NMD
Pathogenic variant (ClinVar)
Tuberous sclerosis syndrome
Tuberous sclerosis 2
See cases
pathogenicClinVar OMIM
Variant DBs
Not in dbSNP
Allele 'T' was not found in gnomAD
Protein conservation
SpeciesMatchGeneAAAlignment
Human      1341PLSKSSSSPELQTLQDILGDPGDK
mutated  no alignment    n/a
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
Protein features N/A
Phylogenetic conservation
PhyloPPhastCons
(flanking)-0.9380.04
5.7081
(flanking)6.7391
?
Splice sites No abrogation of potential splice sites predicted by MaxEntScan.
Distance from splice site N/A
Kozak consensus sequence altered? No
poly(A) signal N/A
AA sequence altered Yes
Chromosome 16
Strand 1
Original gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Original cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Wildtype AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEPERPL EARHAVLALL KAIVQGQVRP RATLGWVTSG CPLTVLSLLG
RVWTPASGER LGVLRALFFK VIKDYPSNED LHERLEVFKA LTDNGRHITY LEEELADFVL
QWMDVGLSSE FLLVLVNLVK FNSCYLDEYI ARMVQMICLL CVRTASSVDI EVSLQVLDAV
VCYNCLPAES LPLFIVTLCR TINVKELCEP CWKLMRNLLG THLGHSAIYN MCHLMEDRAY
MEDAPLLRGA VFFVGMALWG AHRLYSLRNS PTSVLPSFYQ AMACPNEVVS YEIVLSITRL
IKKYRKELQV VAWDILLNII ERLLQQLQTL DSPELRTIVH DLLTTVEELC DQNEFHGSQE
RYFELVERCA DQRPESSLLN LISYRAQSIH PAKDGWIQNL QALMERFFRS ESRGAVRIKV
LDVLSFVLLI NRQFYEEELI NSVVISQLSH IPEDKDHQVR KLATQLLVDL AEGCHTHHFN
SLLDIIEKVM ARSLSPPPEL EERDVAAYSA SLEDVKTAVL GLLVILQTKL YTLPASHATR
VYEMLVSHIQ LHYKHSYTLP IASSIRLQAF DFLLLLRADS LHRLGLPNKD GVVRFSPYCV
CDYMEPERGS EKKTSGPLSP PTGPPGPAPA GPAVRLGSVP YSLLFRVLLQ CLKQESDWKV
LKLVLGRLPE SLRYKVLIFT SPCSVDQLCS ALCSMLSGPK TLERLRGAPE GFSRTDLHLA
VVPVLTALIS YHNYLDKTKQ REMVYCLEQG LIHRCASQCV VALSICSVEM PDIIIKALPV
LVVKLTHISA TASMAVPLLE FLSTLARLPH LYRNFAAEQY ASVFAISLPY TNPSKFNQYI
VCLAHHVIAM WFIRCRLPFR KDFVPFITKG LRSNVLLSFD DTPEKDSFRA RSTSLNERPK
SRIQTSLTSA SLGSADENSV AQADDSLKNL HLELTETCLD MMARYVFSNF TAVPKRSPVG
EFLLAGGRTK TWLVGNKLVT VTTSVGTGTR SLLGLDSGEL QSGPESSSSP GVHVRQTKEA
PAKLESQAGQ QVSRGARDRV RSMSGGHGLR VGALDVPASQ FLGSATSPGP RTAPAAKPEK
ASAGTRVPVQ EKTNLAAYVP LLTQGWAEIL VRRPTGNTSW LMSLENPLSP FSSDINNMPL
QELSNALMAA ERFKEHRDTA LYKSLSVPAA STAKPPPLPR SNTDSAVVME EGSPGEVPVL
VEPPGLEDVE AALGMDRRTD AYSRSSSVSS QEEKSLHAEE LVGRGIPIER VVSSEGGRPS
VDLSFQPSQP LSKSSSSPEL QTLQDILGDP GDKADVGRLS PEVKARSQSG TLDGESAAWS
ASGEDSRGQP EGPLPSSSPR SPSGLRPRGY TISDSAPSRR GKRVERDALK SRATASNAEK
VPGINPSFVF LQLYHSPFFG DESNKPILLP NESQSFERSV QLLDQIPSYD THKIAVLYVG
EGQSNSELAI LSNEHGSYRY TEFLTGLGRL IELKDCQPDK VYLGGLDVCG EDGQFTYCWH
DDIMQAVFHI ATLMPTKDVD KHRCDKKRHL GNDFVSIVYN DSGEDFKLGT IKGQFNFVHV
IVTPLDYECN LVSLQCRKDM EGLVDTSVAK IVSDRNLPFV ARQMALHANM ASQVHHSRSN
PTDIYPSKWI ARLRHIKRLR QRICEEAAYS NPSLPLVHPP SHSKAPAQTP AEPTPGYEVG
QRKRLISSVE DFTEFV*
Mutated AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEPERPL EARHAVLALL KAIVQGQVRP RATLGWVTSG CPLTVLSLLG
RVWTPASGER LGVLRALFFK VIKDYPSNED LHERLEVFKA LTDNGRHITY LEEELADFVL
QWMDVGLSSE FLLVLVNLVK FNSCYLDEYI ARMVQMICLL CVRTASSVDI EVSLQVLDAV
VCYNCLPAES LPLFIVTLCR TINVKELCEP CWKLMRNLLG THLGHSAIYN MCHLMEDRAY
MEDAPLLRGA VFFVGMALWG AHRLYSLRNS PTSVLPSFYQ AMACPNEVVS YEIVLSITRL
IKKYRKELQV VAWDILLNII ERLLQQLQTL DSPELRTIVH DLLTTVEELC DQNEFHGSQE
RYFELVERCA DQRPESSLLN LISYRAQSIH PAKDGWIQNL QALMERFFRS ESRGAVRIKV
LDVLSFVLLI NRQFYEEELI NSVVISQLSH IPEDKDHQVR KLATQLLVDL AEGCHTHHFN
SLLDIIEKVM ARSLSPPPEL EERDVAAYSA SLEDVKTAVL GLLVILQTKL YTLPASHATR
VYEMLVSHIQ LHYKHSYTLP IASSIRLQAF DFLLLLRADS LHRLGLPNKD GVVRFSPYCV
CDYMEPERGS EKKTSGPLSP PTGPPGPAPA GPAVRLGSVP YSLLFRVLLQ CLKQESDWKV
LKLVLGRLPE SLRYKVLIFT SPCSVDQLCS ALCSMLSGPK TLERLRGAPE GFSRTDLHLA
VVPVLTALIS YHNYLDKTKQ REMVYCLEQG LIHRCASQCV VALSICSVEM PDIIIKALPV
LVVKLTHISA TASMAVPLLE FLSTLARLPH LYRNFAAEQY ASVFAISLPY TNPSKFNQYI
VCLAHHVIAM WFIRCRLPFR KDFVPFITKG LRSNVLLSFD DTPEKDSFRA RSTSLNERPK
SRIQTSLTSA SLGSADENSV AQADDSLKNL HLELTETCLD MMARYVFSNF TAVPKRSPVG
EFLLAGGRTK TWLVGNKLVT VTTSVGTGTR SLLGLDSGEL QSGPESSSSP GVHVRQTKEA
PAKLESQAGQ QVSRGARDRV RSMSGGHGLR VGALDVPASQ FLGSATSPGP RTAPAAKPEK
ASAGTRVPVQ EKTNLAAYVP LLTQGWAEIL VRRPTGNTSW LMSLENPLSP FSSDINNMPL
QELSNALMAA ERFKEHRDTA LYKSLSVPAA STAKPPPLPR SNTDSAVVME EGSPGEVPVL
VEPPGLEDVE AALGMDRRTD AYSRSSSVSS QEEKSLHAEE LVGRGIPIER VVSSEGGRPS
VDLSFQPSQP LSKSSSSPEL *
Position of stopcodon in wt / mu CDS 5271 / 4023
Position (AA) of stopcodon in wt / mu AA sequence 1757 / 1341
Position of stopcodon in wt / mu cDNA 5387 / 4139
Position of start ATG in wt / mu cDNA 117 / 117
Last intron/exon boundary 5222
Theoretical NMD boundary in CDS 5055
Length of CDS 5271
Coding sequence (CDS) position 4021
cDNA position 4137
gDNA position 36430
Chromosomal position 2084396
Speed 0.12 s

All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project

Back to summary table

Yum, tasty mutations...

MutationT@ster 2025

Variant:

16:2084396C>T_6_ENST00000645186

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr16:2084396C>T (GRCh38)
Gene symbol TSC2
Gene constraints LOEUF: 0.61, LOF (oe): 0.27, misssense (oe): 1.10, synonymous (oe): 1.24 ? (gnomAD)
Ensembl transcript ID ENST00000645186.2
Genbank transcript ID
UniProt / AlphaMissense peptide N/A
Variant type Single base exchange
Gene region CDS
DNA changes c.4264C>T
g.36430C>T
AA changes Q1422* Score: 6.0?
Frameshift No
Length of protein NMD
Pathogenic variant (ClinVar)
Tuberous sclerosis syndrome
Tuberous sclerosis 2
See cases
pathogenicClinVar OMIM
Variant DBs
Not in dbSNP
Allele 'T' was not found in gnomAD
Protein conservation
SpeciesMatchGeneAAAlignment
Human      1422PLSKSSSSPELQTLQDILGDPGDK
mutated  no alignment    n/a
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
Protein features N/A
Phylogenetic conservation
PhyloPPhastCons
(flanking)-0.9380.04
5.7081
(flanking)6.7391
?
Splice sites No abrogation of potential splice sites predicted by MaxEntScan.
Distance from splice site N/A
Kozak consensus sequence altered? No
poly(A) signal N/A
AA sequence altered Yes
Chromosome 16
Strand 1
Original gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Original cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Wildtype AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSLRIA RPPKQGLNNS
PPVKEFKESS AAEAFRCRSI SVSEHVVRSR IQTSLTSASL GSADENSVAQ ADDSLKNLHL
ELTETCLDMM ARYVFSNFTA VPKRSPVGEF LLAGGRTKTW LVGNKLVTVT TSVGTGTRSL
LGLDSGELQS GPESSSSPGV HVRQTKEAPA KLESQAGQQV SRGARDRVRS MSGGHGLRVG
ALDVPASQFL GSATSPGPRT APAAKPEKAS AGTRVPVQEK TNLAAYVPLL TQGWAEILVR
RPTGNTSWLM SLENPLSPFS SDINNMPLQE LSNALMAAER FKEHRDTALY KSLSVPAAST
AKPPPLPRSN TVASFSSLYQ SSCQGQLHRS VSWAGIASQR EAVGCRAPLC LIGAVLVASS
AHPHDSAVVM EEGSPGEVPV LVEPPGLEDV EAALGMDRRT DAYSRSSSVS SQEEKSLHAE
ELVGRGIPIE RVVSSEGGRP SVDLSFQPSQ PLSKSSSSPE LQTLQDILGD PGDKADVGRL
SPEVKARSQS GTLDGESAAW SASGEDSRGQ PEGPLPSSSP RSPSGLRPRG YTISDSAPSR
RGKRVERDAL KSRATASNAE KVPGINPSFV FLQLYHSPFF GDESNKPILL PNESQSFERS
VQLLDQIPSY DTHKIAVLYV GEGQSNSELA ILSNEHGSYR YTEFLTGLGR LIELKDCQPD
KVYLGGLDVC GEDGQFTYCW HDDIMQAVFH IATLMPTKDV DKHRCDKKRH LGNDFVSIVY
NDSGEDFKLG TIKGQFNFVH VIVTPLDYEC NLVSLQCRKD MEGLVDTSVA KIVSDRNLPF
VARQMALHAN MASQVHHSRS NPTDIYPSKW IARLRHIKRL RQRICEEAAY SNPSLPLVHP
PSHSKAPAQT PAEPTPGYEV GQRKRLISSV EDFTEFV*
Mutated AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSLRIA RPPKQGLNNS
PPVKEFKESS AAEAFRCRSI SVSEHVVRSR IQTSLTSASL GSADENSVAQ ADDSLKNLHL
ELTETCLDMM ARYVFSNFTA VPKRSPVGEF LLAGGRTKTW LVGNKLVTVT TSVGTGTRSL
LGLDSGELQS GPESSSSPGV HVRQTKEAPA KLESQAGQQV SRGARDRVRS MSGGHGLRVG
ALDVPASQFL GSATSPGPRT APAAKPEKAS AGTRVPVQEK TNLAAYVPLL TQGWAEILVR
RPTGNTSWLM SLENPLSPFS SDINNMPLQE LSNALMAAER FKEHRDTALY KSLSVPAAST
AKPPPLPRSN TVASFSSLYQ SSCQGQLHRS VSWAGIASQR EAVGCRAPLC LIGAVLVASS
AHPHDSAVVM EEGSPGEVPV LVEPPGLEDV EAALGMDRRT DAYSRSSSVS SQEEKSLHAE
ELVGRGIPIE RVVSSEGGRP SVDLSFQPSQ PLSKSSSSPE L*
Position of stopcodon in wt / mu CDS 5514 / 4266
Position (AA) of stopcodon in wt / mu AA sequence 1838 / 1422
Position of stopcodon in wt / mu cDNA 5624 / 4376
Position of start ATG in wt / mu cDNA 111 / 111
Last intron/exon boundary 5459
Theoretical NMD boundary in CDS 5298
Length of CDS 5514
Coding sequence (CDS) position 4264
cDNA position 4374
gDNA position 36430
Chromosomal position 2084396
Speed 0.11 s

All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project

Back to summary table

Yum, tasty mutations...

MutationT@ster 2025

Variant:

16:2084396C>T_4_ENST00000382538

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr16:2084396C>T (GRCh38)
Gene symbol TSC2
Gene constraints LOEUF: 0.17, LOF (oe): 0.12, misssense (oe): 0.98, synonymous (oe): 1.29 ? (gnomAD)
Ensembl transcript ID ENST00000382538.10
Genbank transcript ID NM_001406687 (by similarity), NM_001406692 (by similarity), NM_001406697 (by similarity), NM_001406698 (by similarity), NM_001406694 (by similarity), NM_001406695 (by similarity), NM_001406696 (by similarity), NM_001406681 (by similarity), NM_001406677 (by similarity), NM_001406675 (by similarity), NM_001406676 (by similarity), NM_001318829 (by similarity), NM_001406679 (by similarity), NM_001406686 (by similarity)
UniProt / AlphaMissense peptide TSC2_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.3829C>T
g.36430C>T
AA changes Q1277* Score: 6.0?
Frameshift No
Length of protein NMD
Pathogenic variant (ClinVar)
Tuberous sclerosis syndrome
Tuberous sclerosis 2
See cases
pathogenicClinVar OMIM
Variant DBs
Not in dbSNP
Allele 'T' was not found in gnomAD
Protein conservation
SpeciesMatchGeneAAAlignment
Human      1277PLSKSSSSPELQTLQDILGDPGDK
mutated  no alignment    n/a
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
Protein features
Start (aa)End (aa)FeatureDetails 
11807CHAINlost
13311352REGIONlost
13371337MOD_RESPhosphoserinelost
13381338MOD_RESPhosphoserinelost
13461346MOD_RESPhosphoserinelost
13641364MOD_RESPhosphoserinelost
13641488REGIONlost
13701394COMPBIASPolar residueslost
13871387MOD_RESPhosphoserinelost
14111411MOD_RESPhosphoserinelost
14181418MOD_RESPhosphoserinelost
14201420MOD_RESPhosphoserinelost
14521452MOD_RESPhosphoserinelost
14621462MOD_RESPhosphothreoninelost
14691484COMPBIASBasic and acidic residueslost
15311758DOMAINRap-GAPlost
17641764MOD_RESPhosphoserinelost
17651793REGIONlost
17981798MOD_RESPhosphoserinelost
17991799MOD_RESPhosphoserinelost
Phylogenetic conservation
PhyloPPhastCons
(flanking)-0.9380.04
5.7081
(flanking)6.7391
?
Splice sites No abrogation of potential splice sites predicted by MaxEntScan.
Distance from splice site N/A
Kozak consensus sequence altered? No
poly(A) signal N/A
AA sequence altered Yes
Chromosome 16
Strand 1
Original gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Original cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Wildtype AA sequence MECGLNNRIR MIGQICEVAK TKKFEEHAVE ALWKAVADLL QPERPLEARH AVLALLKAIV
QGQGERLGVL RALFFKVIKD YPSNEDLHER LEVFKALTDN GRHITYLEEE LADFVLQWMD
VGLSSEFLLV LVNLVKFNSC YLDEYIARMV QMICLLCVRT ASSVDIEVSL QVLDAVVCYN
CLPAESLPLF IVTLCRTINV KELCEPCWKL MRNLLGTHLG HSAIYNMCHL MEDRAYMEDA
PLLRGAVFFV GMALWGAHRL YSLRNSPTSV LPSFYQAMAC PNEVVSYEIV LSITRLIKKY
RKELQVVAWD ILLNIIERLL QQLQTLDSPE LRTIVHDLLT TVEELCDQNE FHGSQERYFE
LVERCADQRP ESSLLNLISY RAQSIHPAKD GWIQNLQALM ERFFRSESRG AVRIKVLDVL
SFVLLINRQF YEEELINSVV ISQLSHIPED KDHQVRKLAT QLLVDLAEGC HTHHFNSLLD
IIEKVMARSL SPPPELEERD VAAYSASLED VKTAVLGLLV ILQTKLYTLP ASHATRVYEM
LVSHIQLHYK HSYTLPIASS IRLQAFDFLL LLRADSLHRL GLPNKDGVVR FSPYCVCDYM
EPERGSEKKT SGPLSPPTGP PGPAPAGPAV RLGSVPYSLL FRVLLQCLKQ ESDWKVLKLV
LGRLPESLRY KVLIFTSPCS VDQLCSALCS MLSGPKTLER LRGAPEGFSR TDLHLAVVPV
LTALISYHNY LDKTKQREMV YCLEQGLIHR CASQCVVALS ICSVEMPDII IKALPVLVVK
LTHISATASM AVPLLEFLST LARLPHLYRN FAAEQYASVF AISLPYTNPS KFNQYIVCLA
HHVIAMWFIR CRLPFRKDFV PFITKGLRSN VLLSFDDTPE KDSFRARSTS LNERPKSRIQ
TSLTSASLGS ADENSVAQAD DSLKNLHLEL TETCLDMMAR YVFSNFTAVP KRSPVGEFLL
AGGRTKTWLV GNKLVTVTTS VGTGTRSLLG LDSGELQSGP ESSSSPGVHV RQTKEAPAKL
ESQAGQQVSR GARDRVRSMS GGHGLRVGAL DVPASQFLGS ATSPGPRTAP AAKPEKASAG
TRVPVQEKTN LAAYVPLLTQ GWAEILVRRP TGNTSWLMSL ENPLSPFSSD INNMPLQELS
NALMAAERFK EHRDTALYKS LSVPAASTAK PPPLPRSNTD SAVVMEEGSP GEVPVLVEPP
GLEDVEAALG MDRRTDAYSR SSSVSSQEEK SLHAEELVGR GIPIERVVSS EGGRPSVDLS
FQPSQPLSKS SSSPELQTLQ DILGDPGDKA DVGRLSPEVK ARSQSGTLDG ESAAWSASGE
DSRGQPEGPL PSSSPRSPSG LRPRGYTISD SAPSRRGKRV ERDALKSRAT ASNAEKVPGI
NPSFVFLQLY HSPFFGDESN KPILLPNESQ SFERSVQLLD QIPSYDTHKI AVLYVGEGQS
NSELAILSNE HGSYRYTEFL TGLGRLIELK DCQPDKVYLG GLDVCGEDGQ FTYCWHDDIM
QAVFHIATLM PTKDVDKHRC DKKRHLGNDF VSIVYNDSGE DFKLGTIKGQ FNFVHVIVTP
LDYECNLVSL QCRKDMEGLV DTSVAKIVSD RNLPFVARQM ALHANMASQV HHSRSNPTDI
YPSKWIARLR HIKRLRQRIC EEAAYSNPSL PLVHPPSHSK APAQTPAEPT PGYEVGQRKR
LISSVEDFTE FV*
Mutated AA sequence MECGLNNRIR MIGQICEVAK TKKFEEHAVE ALWKAVADLL QPERPLEARH AVLALLKAIV
QGQGERLGVL RALFFKVIKD YPSNEDLHER LEVFKALTDN GRHITYLEEE LADFVLQWMD
VGLSSEFLLV LVNLVKFNSC YLDEYIARMV QMICLLCVRT ASSVDIEVSL QVLDAVVCYN
CLPAESLPLF IVTLCRTINV KELCEPCWKL MRNLLGTHLG HSAIYNMCHL MEDRAYMEDA
PLLRGAVFFV GMALWGAHRL YSLRNSPTSV LPSFYQAMAC PNEVVSYEIV LSITRLIKKY
RKELQVVAWD ILLNIIERLL QQLQTLDSPE LRTIVHDLLT TVEELCDQNE FHGSQERYFE
LVERCADQRP ESSLLNLISY RAQSIHPAKD GWIQNLQALM ERFFRSESRG AVRIKVLDVL
SFVLLINRQF YEEELINSVV ISQLSHIPED KDHQVRKLAT QLLVDLAEGC HTHHFNSLLD
IIEKVMARSL SPPPELEERD VAAYSASLED VKTAVLGLLV ILQTKLYTLP ASHATRVYEM
LVSHIQLHYK HSYTLPIASS IRLQAFDFLL LLRADSLHRL GLPNKDGVVR FSPYCVCDYM
EPERGSEKKT SGPLSPPTGP PGPAPAGPAV RLGSVPYSLL FRVLLQCLKQ ESDWKVLKLV
LGRLPESLRY KVLIFTSPCS VDQLCSALCS MLSGPKTLER LRGAPEGFSR TDLHLAVVPV
LTALISYHNY LDKTKQREMV YCLEQGLIHR CASQCVVALS ICSVEMPDII IKALPVLVVK
LTHISATASM AVPLLEFLST LARLPHLYRN FAAEQYASVF AISLPYTNPS KFNQYIVCLA
HHVIAMWFIR CRLPFRKDFV PFITKGLRSN VLLSFDDTPE KDSFRARSTS LNERPKSRIQ
TSLTSASLGS ADENSVAQAD DSLKNLHLEL TETCLDMMAR YVFSNFTAVP KRSPVGEFLL
AGGRTKTWLV GNKLVTVTTS VGTGTRSLLG LDSGELQSGP ESSSSPGVHV RQTKEAPAKL
ESQAGQQVSR GARDRVRSMS GGHGLRVGAL DVPASQFLGS ATSPGPRTAP AAKPEKASAG
TRVPVQEKTN LAAYVPLLTQ GWAEILVRRP TGNTSWLMSL ENPLSPFSSD INNMPLQELS
NALMAAERFK EHRDTALYKS LSVPAASTAK PPPLPRSNTD SAVVMEEGSP GEVPVLVEPP
GLEDVEAALG MDRRTDAYSR SSSVSSQEEK SLHAEELVGR GIPIERVVSS EGGRPSVDLS
FQPSQPLSKS SSSPEL*
Position of stopcodon in wt / mu CDS 5079 / 3831
Position (AA) of stopcodon in wt / mu AA sequence 1693 / 1277
Position of stopcodon in wt / mu cDNA 5174 / 3926
Position of start ATG in wt / mu cDNA 96 / 96
Last intron/exon boundary 5009
Theoretical NMD boundary in CDS 4863
Length of CDS 5079
Coding sequence (CDS) position 3829
cDNA position 3924
gDNA position 36430
Chromosomal position 2084396
Speed 0.11 s

All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project

Back to summary table

Yum, tasty mutations...

MutationT@ster 2025

Variant:

16:2084396C>T_8_ENST00000644335

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr16:2084396C>T (GRCh38)
Gene symbol TSC2
Gene constraints LOEUF: 0.18, LOF (oe): 0.12, misssense (oe): 0.98, synonymous (oe): 1.28 ? (gnomAD)
Ensembl transcript ID ENST00000644335.1
Genbank transcript ID
UniProt / AlphaMissense peptide N/A
Variant type Single base exchange
Gene region CDS
DNA changes c.3976C>T
g.36430C>T
AA changes Q1326* Score: 6.0?
Frameshift No
Length of protein NMD
Pathogenic variant (ClinVar)
Tuberous sclerosis syndrome
Tuberous sclerosis 2
See cases
pathogenicClinVar OMIM
Variant DBs
Not in dbSNP
Allele 'T' was not found in gnomAD
Protein conservation
SpeciesMatchGeneAAAlignment
Human      1326PLSKSSSSPELQTLQDILGDPGDK
mutated  no alignment    n/a
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
Protein features N/A
Phylogenetic conservation
PhyloPPhastCons
(flanking)-0.9380.04
5.7081
(flanking)6.7391
?
Splice sites No abrogation of potential splice sites predicted by MaxEntScan.
Distance from splice site N/A
Kozak consensus sequence altered? No
poly(A) signal N/A
AA sequence altered Yes
Chromosome 16
Strand 1
Original gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Original cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Wildtype AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSRIQT SLTSASLGSA
DENSVAQADD SLKNLHLELT ETCLDMMARY VFSNFTAVPK RSPVGEFLLA GGRTKTWLVG
NKLVTVTTSV GTGTRSLLGL DSGELQSGPE SSSSPGVHVR QTKEAPAKLE SQAGQQVSRG
ARDRVRSMSG GHGLRVGALD VPASQFLGSA TSPGPRTAPA AKPEKASAGT RVPVQEKTNL
AAYVPLLTQG WAEILVRRPT GNTSWLMSLE NPLSPFSSDI NNMPLQELSN ALMAAERFKE
HRDTALYKSL SVPAASTAKP PPLPRSNTDS AVVMEEGSPG EVPVLVEPPG LEDVEAALGM
DRRTDAYSRS SSVSSQEEKS LHAEELVGRG IPIERVVSSE GGRPSVDLSF QPSQPLSKSS
SSPELQTLQD ILGDPGDKAD VGRLSPEVKA RSQSGTLDGE SAAWSASGED SRGQPEGPLP
SSSPRSPSGL RPRGYTISDS APSRRGKRVE RDALKSRATA SNAEKVPGIN PSFVFLQLYH
SPFFGDESNK PILLPNESFE RSVQLLDQIP SYDTHKIAVL YVGEGQSNSE LAILSNEHGS
YRYTEFLTGL GRLIELKDCQ PDKVYLGGLD VCGEDGQFTY CWHDDIMQAV FHIATLMPTK
DVDKHRCDKK RHLGNDFVSI VYNDSGEDFK LGTIKGQFNF VHVIVTPLDY ECNLVSLQCR
KDMEGLVDTS VAKIVSDRNL PFVARQMALH ANMASQVHHS RSNPTDIYPS KWIARLRHIK
RLRQRICEEA AYSNPSLPLV HPPSHSKAPA QTPAEPTPGY EVGQRKRLIS SVEDFTEFV*
Mutated AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSRIQT SLTSASLGSA
DENSVAQADD SLKNLHLELT ETCLDMMARY VFSNFTAVPK RSPVGEFLLA GGRTKTWLVG
NKLVTVTTSV GTGTRSLLGL DSGELQSGPE SSSSPGVHVR QTKEAPAKLE SQAGQQVSRG
ARDRVRSMSG GHGLRVGALD VPASQFLGSA TSPGPRTAPA AKPEKASAGT RVPVQEKTNL
AAYVPLLTQG WAEILVRRPT GNTSWLMSLE NPLSPFSSDI NNMPLQELSN ALMAAERFKE
HRDTALYKSL SVPAASTAKP PPLPRSNTDS AVVMEEGSPG EVPVLVEPPG LEDVEAALGM
DRRTDAYSRS SSVSSQEEKS LHAEELVGRG IPIERVVSSE GGRPSVDLSF QPSQPLSKSS
SSPEL*
Position of stopcodon in wt / mu CDS 5220 / 3978
Position (AA) of stopcodon in wt / mu AA sequence 1740 / 1326
Position of stopcodon in wt / mu cDNA 5320 / 4078
Position of start ATG in wt / mu cDNA 101 / 101
Last intron/exon boundary 5155
Theoretical NMD boundary in CDS 5004
Length of CDS 5220
Coding sequence (CDS) position 3976
cDNA position 4076
gDNA position 36430
Chromosomal position 2084396
Speed 0.11 s

All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project

Back to summary table

Yum, tasty mutations...

MutationT@ster 2025

Variant:

16:2084396C>T_9_ENST00000646388

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr16:2084396C>T (GRCh38)
Gene symbol TSC2
Gene constraints LOEUF: 0.21, LOF (oe): 0.15, misssense (oe): 0.99, synonymous (oe): 1.28 ? (gnomAD)
Ensembl transcript ID ENST00000646388.1
Genbank transcript ID
UniProt / AlphaMissense peptide N/A
Variant type Single base exchange
Gene region CDS
DNA changes c.4174C>T
g.36430C>T
AA changes Q1392* Score: 6.0?
Frameshift No
Length of protein NMD
Pathogenic variant (ClinVar)
Tuberous sclerosis syndrome
Tuberous sclerosis 2
See cases
pathogenicClinVar OMIM
Variant DBs
Not in dbSNP
Allele 'T' was not found in gnomAD
Protein conservation
SpeciesMatchGeneAAAlignment
Human      1392PLSKSSSSPELQTLQDILGDPGDK
mutated  no alignment    n/a
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
Protein features N/A
Phylogenetic conservation
PhyloPPhastCons
(flanking)-0.9380.04
5.7081
(flanking)6.7391
?
Splice sites No abrogation of potential splice sites predicted by MaxEntScan.
Distance from splice site N/A
Kozak consensus sequence altered? No
poly(A) signal N/A
AA sequence altered Yes
Chromosome 16
Strand 1
Original gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Original cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Wildtype AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSLRIA RPPKQGLNNS
PPVKEFKESS AAEAFRCRSI SVSEHVVRSR IQTSLTSASL GSADENSVAQ ADDSLKNLHL
ELTETCLDMM ARYVFSNFTA VPKRSPVGEF LLAGGRTKTW LVGNKLVTVT TSVGTGTRSL
LGLDSGELQS GPESSSSPGV HVRQTKEAPA KLESQAGQQV SRGARDRVRS MSGGHGLRVG
ALDVPASQFL GSATSPGPRT APAAKPEKAS AGTRVPVQEK TNLAAYVPLL TQGWAEILVR
RPTGNTSWLM SLENPLSPFS SDINNMPLQE LSNALMAAER FKEHRDTALY KSLSVPAAST
AKPPPLPRSN TVASFSSLYQ SSCQGQLHRS VSWADSAVVM EEGSPGEVPV LVEPPGLEDV
EAALGMDRRT DAYSRSSSVS SQEEKSLHAE ELVGRGIPIE RVVSSEGGRP SVDLSFQPSQ
PLSKSSSSPE LQTLQDILGD PGDKADVGRL SPEVKARSQS GTLDGESAAW SASGEDSRGQ
PEGPLPSSSP RSPSGLRPRG YTISDSAPSR RGKRVERDAL KSRATASNAE KVPGINPSFV
FLQLYHSPFF GDESNKPILL PNESFERSVQ LLDQIPSYDT HKIAVLYVGE GQSNSELAIL
SNEHGSYRYT EFLTGLGRLI ELKDCQPDKV YLGGLDVCGE DGQFTYCWHD DIMQAVFHIA
TLMPTKDVDK HRCDKKRHLG NDFVSIVYND SGEDFKLGTI KGQFNFVHVI VTPLDYECNL
VSLQCRKDME GLVDTSVAKI VSDRNLPFVA RQMALHANMA SQVHHSRSNP TDIYPSKWIA
RLRHIKRLRQ RICEEAAYSN PSLPLVHPPS HSKAPAQTPA EPTPGYEVGQ RKRLISSVED
FTEFV*
Mutated AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSLRIA RPPKQGLNNS
PPVKEFKESS AAEAFRCRSI SVSEHVVRSR IQTSLTSASL GSADENSVAQ ADDSLKNLHL
ELTETCLDMM ARYVFSNFTA VPKRSPVGEF LLAGGRTKTW LVGNKLVTVT TSVGTGTRSL
LGLDSGELQS GPESSSSPGV HVRQTKEAPA KLESQAGQQV SRGARDRVRS MSGGHGLRVG
ALDVPASQFL GSATSPGPRT APAAKPEKAS AGTRVPVQEK TNLAAYVPLL TQGWAEILVR
RPTGNTSWLM SLENPLSPFS SDINNMPLQE LSNALMAAER FKEHRDTALY KSLSVPAAST
AKPPPLPRSN TVASFSSLYQ SSCQGQLHRS VSWADSAVVM EEGSPGEVPV LVEPPGLEDV
EAALGMDRRT DAYSRSSSVS SQEEKSLHAE ELVGRGIPIE RVVSSEGGRP SVDLSFQPSQ
PLSKSSSSPE L*
Position of stopcodon in wt / mu CDS 5418 / 4176
Position (AA) of stopcodon in wt / mu AA sequence 1806 / 1392
Position of stopcodon in wt / mu cDNA 5504 / 4262
Position of start ATG in wt / mu cDNA 87 / 87
Last intron/exon boundary 5339
Theoretical NMD boundary in CDS 5202
Length of CDS 5418
Coding sequence (CDS) position 4174
cDNA position 4260
gDNA position 36430
Chromosomal position 2084396
Speed 0.11 s

All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project

Back to summary table

Yum, tasty mutations...

MutationT@ster 2025

Variant:

16:2084396C>T_7_ENST00000401874

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr16:2084396C>T (GRCh38)
Gene symbol TSC2
Gene constraints LOEUF: 0.18, LOF (oe): 0.12, misssense (oe): 0.98, synonymous (oe): 1.28 ? (gnomAD)
Ensembl transcript ID ENST00000401874.7
Genbank transcript ID NM_001077183 (by similarity), NM_001406673 (by similarity)
UniProt / AlphaMissense peptide TSC2_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.3973C>T
g.36430C>T
AA changes Q1325* Score: 6.0?
Frameshift No
Length of protein NMD
Pathogenic variant (ClinVar)
Tuberous sclerosis syndrome
Tuberous sclerosis 2
See cases
pathogenicClinVar OMIM
Variant DBs
Not in dbSNP
Allele 'T' was not found in gnomAD
Protein conservation
SpeciesMatchGeneAAAlignment
Human      1325PLSKSSSSPELQTLQDILGDPGDK
mutated  no alignment    n/a
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
Protein features
Start (aa)End (aa)FeatureDetails 
11807CHAINlost
13311352REGIONlost
13371337MOD_RESPhosphoserinelost
13381338MOD_RESPhosphoserinelost
13461346MOD_RESPhosphoserinelost
13641364MOD_RESPhosphoserinelost
13641488REGIONlost
13701394COMPBIASPolar residueslost
13871387MOD_RESPhosphoserinelost
14111411MOD_RESPhosphoserinelost
14181418MOD_RESPhosphoserinelost
14201420MOD_RESPhosphoserinelost
14521452MOD_RESPhosphoserinelost
14621462MOD_RESPhosphothreoninelost
14691484COMPBIASBasic and acidic residueslost
15311758DOMAINRap-GAPlost
17641764MOD_RESPhosphoserinelost
17651793REGIONlost
17981798MOD_RESPhosphoserinelost
17991799MOD_RESPhosphoserinelost
Phylogenetic conservation
PhyloPPhastCons
(flanking)-0.9380.04
5.7081
(flanking)6.7391
?
Splice sites No abrogation of potential splice sites predicted by MaxEntScan.
Distance from splice site N/A
Kozak consensus sequence altered? No
poly(A) signal N/A
AA sequence altered Yes
Chromosome 16
Strand 1
Original gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Original cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Wildtype AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKRIQTS LTSASLGSAD
ENSVAQADDS LKNLHLELTE TCLDMMARYV FSNFTAVPKR SPVGEFLLAG GRTKTWLVGN
KLVTVTTSVG TGTRSLLGLD SGELQSGPES SSSPGVHVRQ TKEAPAKLES QAGQQVSRGA
RDRVRSMSGG HGLRVGALDV PASQFLGSAT SPGPRTAPAA KPEKASAGTR VPVQEKTNLA
AYVPLLTQGW AEILVRRPTG NTSWLMSLEN PLSPFSSDIN NMPLQELSNA LMAAERFKEH
RDTALYKSLS VPAASTAKPP PLPRSNTDSA VVMEEGSPGE VPVLVEPPGL EDVEAALGMD
RRTDAYSRSS SVSSQEEKSL HAEELVGRGI PIERVVSSEG GRPSVDLSFQ PSQPLSKSSS
SPELQTLQDI LGDPGDKADV GRLSPEVKAR SQSGTLDGES AAWSASGEDS RGQPEGPLPS
SSPRSPSGLR PRGYTISDSA PSRRGKRVER DALKSRATAS NAEKVPGINP SFVFLQLYHS
PFFGDESNKP ILLPNESQSF ERSVQLLDQI PSYDTHKIAV LYVGEGQSNS ELAILSNEHG
SYRYTEFLTG LGRLIELKDC QPDKVYLGGL DVCGEDGQFT YCWHDDIMQA VFHIATLMPT
KDVDKHRCDK KRHLGNDFVS IVYNDSGEDF KLGTIKGQFN FVHVIVTPLD YECNLVSLQC
RKDMEGLVDT SVAKIVSDRN LPFVARQMAL HANMASQVHH SRSNPTDIYP SKWIARLRHI
KRLRQRICEE AAYSNPSLPL VHPPSHSKAP AQTPAEPTPG YEVGQRKRLI SSVEDFTEFV
*
Mutated AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKRIQTS LTSASLGSAD
ENSVAQADDS LKNLHLELTE TCLDMMARYV FSNFTAVPKR SPVGEFLLAG GRTKTWLVGN
KLVTVTTSVG TGTRSLLGLD SGELQSGPES SSSPGVHVRQ TKEAPAKLES QAGQQVSRGA
RDRVRSMSGG HGLRVGALDV PASQFLGSAT SPGPRTAPAA KPEKASAGTR VPVQEKTNLA
AYVPLLTQGW AEILVRRPTG NTSWLMSLEN PLSPFSSDIN NMPLQELSNA LMAAERFKEH
RDTALYKSLS VPAASTAKPP PLPRSNTDSA VVMEEGSPGE VPVLVEPPGL EDVEAALGMD
RRTDAYSRSS SVSSQEEKSL HAEELVGRGI PIERVVSSEG GRPSVDLSFQ PSQPLSKSSS
SPEL*
Position of stopcodon in wt / mu CDS 5223 / 3975
Position (AA) of stopcodon in wt / mu AA sequence 1741 / 1325
Position of stopcodon in wt / mu cDNA 5329 / 4081
Position of start ATG in wt / mu cDNA 107 / 107
Last intron/exon boundary 5164
Theoretical NMD boundary in CDS 5007
Length of CDS 5223
Coding sequence (CDS) position 3973
cDNA position 4079
gDNA position 36430
Chromosomal position 2084396
Speed 0.12 s

All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project

Back to summary table

Yum, tasty mutations...

MutationT@ster 2025

Variant:

16:2084396C>T_5_ENST00000219476

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr16:2084396C>T (GRCh38)
Gene symbol TSC2
Gene constraints LOEUF: 0.20, LOF (oe): 0.15, misssense (oe): 0.99, synonymous (oe): 1.28 ? (gnomAD)
Ensembl transcript ID ENST00000219476.9
Genbank transcript ID NM_000548 (exact from MANE), NM_001406680 (by similarity)
UniProt / AlphaMissense peptide TSC2_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.4174C>T
g.36430C>T
AA changes Q1392* Score: 6.0?
Frameshift No
Length of protein NMD
Pathogenic variant (ClinVar)
Tuberous sclerosis syndrome
Tuberous sclerosis 2
See cases
pathogenicClinVar OMIM
Variant DBs
Not in dbSNP
Allele 'T' was not found in gnomAD
Protein conservation
SpeciesMatchGeneAAAlignment
Human      1392PLSKSSSSPELQTLQDILGDPGDKADVGRLSPEVKARSQSGTLDGESAAWSASGEDSRGQPEGPLPSSSPRSPSGLRPRGYTISDSAPSRRGKRVERDALKSRATASNAEKVPGINPSFVFLQLYHSPFFGD
mutated  no alignment    n/a
Ptroglodytes  all identical    1274PLSKSSSSPELQTLQDILGDPGDKADVGRLSPEVKARSQSGTLDGESAAWSASGEDSRGQPEGPLPSSSPRSPSGLRPRGYTISDSAPSRRGK
Mmulatta  partly conserved    1592PLSKSSSSPELQTLQDILGDPGDKADVGRLSPEVKARSQSGILDGESAAWPASGEDSRGQPEGPLPSSSPRSPSGLRPRGYTISDSAPSRRGRRVERDAFKSRATASNAEKVPGINPSFV
Fcatus  partly conserved    1389PLSKSSSSPELQTLQDTLGDPGDKADVGRLSPEAKARSQSGTLDGAGAAWSTPGEESQGRGPARPEGPLPSGCPRSPGGLRPRGYTISDSAPSRRGKRVERDAFKSRAGASNTEKVP
Mmusculus  partly conserved    1394PLSKSSSSPELQTLQDILGDLGDKIDIGRLSPEAKVRSQSGILDGEAATWSATGEESRITVPPEGPLPSSSPRSPSGLRPRGYTISDSAPSRRGKRVERDNFKSRAAASSAEKVPGI
Ggallus  partly conserved    1414PLSKSSSSPELQTLQEILKDANGREVTRRLSTEVKSKSQSGNLEGEGLGSWLNKGEDARAAGSGGLDGSGPTTSPRSPSGHRPRGYTISDSAPSRRGK
Trubripes  partly conserved    1393GLNKSSSSPELQTLPEAFSKAAMESESATGDVSWSRTPSEGKPPPPPPHLEKMEGTITDANGLEGHGQGSEGPAAGAGRMRLEFPAAPVQ
Drerio  no homologue    
Dmelanogaster  no alignment    n/a
Celegans  no homologue    
Xtropicalis  partly conserved    1398TLSKSSSSPELQTLQELPKELGPTEDIKKPSADFKTLPHVENPLSHRTKSEEERSAGALAKPEGEMRLEPELPVLSPQSPTGHRPRGHTISDSEPSRRG
Protein features
Start (aa)End (aa)FeatureDetails 
11807CHAINlost
13641488REGIONlost
13701394COMPBIASPolar residueslost
14111411MOD_RESPhosphoserinelost
14181418MOD_RESPhosphoserinelost
14201420MOD_RESPhosphoserinelost
14521452MOD_RESPhosphoserinelost
14621462MOD_RESPhosphothreoninelost
14691484COMPBIASBasic and acidic residueslost
15311758DOMAINRap-GAPlost
17641764MOD_RESPhosphoserinelost
17651793REGIONlost
17981798MOD_RESPhosphoserinelost
17991799MOD_RESPhosphoserinelost
Phylogenetic conservation
PhyloPPhastCons
(flanking)-0.9380.04
5.7081
(flanking)6.7391
?
Splice sites No abrogation of potential splice sites predicted by MaxEntScan.
Distance from splice site N/A
Kozak consensus sequence altered? No
poly(A) signal N/A
AA sequence altered Yes
Chromosome 16
Strand 1
Original gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Original cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Wildtype AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSLRIA RPPKQGLNNS
PPVKEFKESS AAEAFRCRSI SVSEHVVRSR IQTSLTSASL GSADENSVAQ ADDSLKNLHL
ELTETCLDMM ARYVFSNFTA VPKRSPVGEF LLAGGRTKTW LVGNKLVTVT TSVGTGTRSL
LGLDSGELQS GPESSSSPGV HVRQTKEAPA KLESQAGQQV SRGARDRVRS MSGGHGLRVG
ALDVPASQFL GSATSPGPRT APAAKPEKAS AGTRVPVQEK TNLAAYVPLL TQGWAEILVR
RPTGNTSWLM SLENPLSPFS SDINNMPLQE LSNALMAAER FKEHRDTALY KSLSVPAAST
AKPPPLPRSN TVASFSSLYQ SSCQGQLHRS VSWADSAVVM EEGSPGEVPV LVEPPGLEDV
EAALGMDRRT DAYSRSSSVS SQEEKSLHAE ELVGRGIPIE RVVSSEGGRP SVDLSFQPSQ
PLSKSSSSPE LQTLQDILGD PGDKADVGRL SPEVKARSQS GTLDGESAAW SASGEDSRGQ
PEGPLPSSSP RSPSGLRPRG YTISDSAPSR RGKRVERDAL KSRATASNAE KVPGINPSFV
FLQLYHSPFF GDESNKPILL PNESQSFERS VQLLDQIPSY DTHKIAVLYV GEGQSNSELA
ILSNEHGSYR YTEFLTGLGR LIELKDCQPD KVYLGGLDVC GEDGQFTYCW HDDIMQAVFH
IATLMPTKDV DKHRCDKKRH LGNDFVSIVY NDSGEDFKLG TIKGQFNFVH VIVTPLDYEC
NLVSLQCRKD MEGLVDTSVA KIVSDRNLPF VARQMALHAN MASQVHHSRS NPTDIYPSKW
IARLRHIKRL RQRICEEAAY SNPSLPLVHP PSHSKAPAQT PAEPTPGYEV GQRKRLISSV
EDFTEFV*
Mutated AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSLRIA RPPKQGLNNS
PPVKEFKESS AAEAFRCRSI SVSEHVVRSR IQTSLTSASL GSADENSVAQ ADDSLKNLHL
ELTETCLDMM ARYVFSNFTA VPKRSPVGEF LLAGGRTKTW LVGNKLVTVT TSVGTGTRSL
LGLDSGELQS GPESSSSPGV HVRQTKEAPA KLESQAGQQV SRGARDRVRS MSGGHGLRVG
ALDVPASQFL GSATSPGPRT APAAKPEKAS AGTRVPVQEK TNLAAYVPLL TQGWAEILVR
RPTGNTSWLM SLENPLSPFS SDINNMPLQE LSNALMAAER FKEHRDTALY KSLSVPAAST
AKPPPLPRSN TVASFSSLYQ SSCQGQLHRS VSWADSAVVM EEGSPGEVPV LVEPPGLEDV
EAALGMDRRT DAYSRSSSVS SQEEKSLHAE ELVGRGIPIE RVVSSEGGRP SVDLSFQPSQ
PLSKSSSSPE L*
Position of stopcodon in wt / mu CDS 5424 / 4176
Position (AA) of stopcodon in wt / mu AA sequence 1808 / 1392
Position of stopcodon in wt / mu cDNA 5534 / 4286
Position of start ATG in wt / mu cDNA 111 / 111
Last intron/exon boundary 5369
Theoretical NMD boundary in CDS 5208
Length of CDS 5424
Coding sequence (CDS) position 4174
cDNA position 4284
gDNA position 36430
Chromosomal position 2084396
Speed 0.13 s

All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project

Back to summary table

Yum, tasty mutations...

MutationT@ster 2025

Variant:

16:2084396C>T_12_ENST00000642365

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr16:2084396C>T (GRCh38)
Gene symbol TSC2
Gene constraints LOEUF: 0.22, LOF (oe): 0.16, misssense (oe): 0.99, synonymous (oe): 1.31 ? (gnomAD)
Ensembl transcript ID ENST00000642365.2
Genbank transcript ID NM_001406663 (by similarity)
UniProt / AlphaMissense peptide N/A
Variant type Single base exchange
Gene region CDS
DNA changes c.4171C>T
g.36430C>T
AA changes Q1391* Score: 6.0?
Frameshift No
Length of protein NMD
Pathogenic variant (ClinVar)
Tuberous sclerosis syndrome
Tuberous sclerosis 2
See cases
pathogenicClinVar OMIM
Variant DBs
Not in dbSNP
Allele 'T' was not found in gnomAD
Protein conservation
SpeciesMatchGeneAAAlignment
Human      1391PLSKSSSSPELQTLQDILGDPGDK
mutated  no alignment    n/a
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
Protein features N/A
Phylogenetic conservation
PhyloPPhastCons
(flanking)-0.9380.04
5.7081
(flanking)6.7391
?
Splice sites No abrogation of potential splice sites predicted by MaxEntScan.
Distance from splice site N/A
Kozak consensus sequence altered? No
poly(A) signal N/A
AA sequence altered Yes
Chromosome 16
Strand 1
Original gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Original cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Wildtype AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSLRIA RPPKQGLNNS
PPVKEFKESS AAEAFRCRSI SVSEHVVRRI QTSLTSASLG SADENSVAQA DDSLKNLHLE
LTETCLDMMA RYVFSNFTAV PKRSPVGEFL LAGGRTKTWL VGNKLVTVTT SVGTGTRSLL
GLDSGELQSG PESSSSPGVH VRQTKEAPAK LESQAGQQVS RGARDRVRSM SGGHGLRVGA
LDVPASQFLG SATSPGPRTA PAAKPEKASA GTRVPVQEKT NLAAYVPLLT QGWAEILVRR
PTGNTSWLMS LENPLSPFSS DINNMPLQEL SNALMAAERF KEHRDTALYK SLSVPAASTA
KPPPLPRSNT VASFSSLYQS SCQGQLHRSV SWADSAVVME EGSPGEVPVL VEPPGLEDVE
AALGMDRRTD AYSRSSSVSS QEEKSLHAEE LVGRGIPIER VVSSEGGRPS VDLSFQPSQP
LSKSSSSPEL QTLQDILGDP GDKADVGRLS PEVKARSQSG TLDGESAAWS ASGEDSRGQP
EGPLPSSSPR SPSGLRPRGY TISDSAPSRR GKRVERDALK SRATASNAEK VPGINPSFVF
LQLYHSPFFG DESNKPILLP NESQSFERSV QLLDQIPSYD THKIAVLYVG EGQSNSELAI
LSNEHGSYRY TEFLTGLGRL IELKDCQPDK VYLGGLDVCG EDGQFTYCWH DDIMQAVFHI
ATLMPTKDVD KHRCDKKRHL GNDFVSIVYN DSGEDFKLGT IKGQFNFVHV IVTPLDYECN
LVSLQCRKDM EGLVDTSVAK IVSDRNLPFV ARQMALHANM ASQVHHSRSN PTDIYPSKWI
ARLRHIKRLR QRICEEAAYS NPSLPLVHPP SHSKAPAQTP AEPTPGYEVG QRKRLISSVE
DFTEFV*
Mutated AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSLRIA RPPKQGLNNS
PPVKEFKESS AAEAFRCRSI SVSEHVVRRI QTSLTSASLG SADENSVAQA DDSLKNLHLE
LTETCLDMMA RYVFSNFTAV PKRSPVGEFL LAGGRTKTWL VGNKLVTVTT SVGTGTRSLL
GLDSGELQSG PESSSSPGVH VRQTKEAPAK LESQAGQQVS RGARDRVRSM SGGHGLRVGA
LDVPASQFLG SATSPGPRTA PAAKPEKASA GTRVPVQEKT NLAAYVPLLT QGWAEILVRR
PTGNTSWLMS LENPLSPFSS DINNMPLQEL SNALMAAERF KEHRDTALYK SLSVPAASTA
KPPPLPRSNT VASFSSLYQS SCQGQLHRSV SWADSAVVME EGSPGEVPVL VEPPGLEDVE
AALGMDRRTD AYSRSSSVSS QEEKSLHAEE LVGRGIPIER VVSSEGGRPS VDLSFQPSQP
LSKSSSSPEL *
Position of stopcodon in wt / mu CDS 5421 / 4173
Position (AA) of stopcodon in wt / mu AA sequence 1807 / 1391
Position of stopcodon in wt / mu cDNA 5492 / 4244
Position of start ATG in wt / mu cDNA 72 / 72
Last intron/exon boundary 5327
Theoretical NMD boundary in CDS 5205
Length of CDS 5421
Coding sequence (CDS) position 4171
cDNA position 4242
gDNA position 36430
Chromosomal position 2084396
Speed 0.12 s

All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project

Back to summary table

Yum, tasty mutations...

MutationT@ster 2025

Variant:

16:2084396C>T_13_ENST00000644329

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr16:2084396C>T (GRCh38)
Gene symbol TSC2
Gene constraints LOEUF: 0.21, LOF (oe): 0.15, misssense (oe): 0.99, synonymous (oe): 1.28 ? (gnomAD)
Ensembl transcript ID ENST00000644329.1
Genbank transcript ID
UniProt / AlphaMissense peptide N/A
Variant type Single base exchange
Gene region CDS
DNA changes c.3973C>T
g.36430C>T
AA changes Q1325* Score: 6.0?
Frameshift No
Length of protein NMD
Pathogenic variant (ClinVar)
Tuberous sclerosis syndrome
Tuberous sclerosis 2
See cases
pathogenicClinVar OMIM
Variant DBs
Not in dbSNP
Allele 'T' was not found in gnomAD
Protein conservation
SpeciesMatchGeneAAAlignment
Human      1325PLSKSSSSPELQTLQDILGDPGDK
mutated  no alignment    n/a
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
Protein features N/A
Phylogenetic conservation
PhyloPPhastCons
(flanking)-0.9380.04
5.7081
(flanking)6.7391
?
Splice sites No abrogation of potential splice sites predicted by MaxEntScan.
Distance from splice site N/A
Kozak consensus sequence altered? No
poly(A) signal N/A
AA sequence altered Yes
Chromosome 16
Strand 1
Original gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Original cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Wildtype AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKRIQTS LTSASLGSAD
ENSVAQADDS LKNLHLELTE TCLDMMARYV FSNFTAVPKR SPVGEFLLAG GRTKTWLVGN
KLVTVTTSVG TGTRSLLGLD SGELQSGPES SSSPGVHVRQ TKEAPAKLES QAGQQVSRGA
RDRVRSMSGG HGLRVGALDV PASQFLGSAT SPGPRTAPAA KPEKASAGTR VPVQEKTNLA
AYVPLLTQGW AEILVRRPTG NTSWLMSLEN PLSPFSSDIN NMPLQELSNA LMAAERFKEH
RDTALYKSLS VPAASTAKPP PLPRSNTDSA VVMEEGSPGE VPVLVEPPGL EDVEAALGMD
RRTDAYSRSS SVSSQEEKSL HAEELVGRGI PIERVVSSEG GRPSVDLSFQ PSQPLSKSSS
SPELQTLQDI LGDPGDKADV GRLSPEVKAR SQSGTLDGES AAWSASGEDS RGQPEGPLPS
SSPRSPSGLR PRGYTISDSA PSRRGKRVER DALKSRATAS NAEKVPGINP SFVFLQLYHS
PFFGDESNKP ILLPNESQSF ERSVQLLDQI PSYDTHKIAV LYVGEGQSNS ELAILSNEHG
SYRYTEFLTG LGRLIELKDC QPDKVYLGGL DVCGEDGQFT YCWHDDIMQA VFHIATLMPT
KDVDKHRCDK KRHLGNDFVS IVYNDSGEDF KLGTIKGQFN FVHVIVTPLD YECNLVSLQC
RKDMEGLVDT SVAKIVSDRN LPFVARQMAL HANVSGGGSR RELVGQAQVP PDSELTPCLR
PQMASQVHHS RSNPTDIYPS KWIARLRHIK RLRQRICEEA AYSNPSLPLV HPPSHSKAPA
QTPAEPTPGY EVGQRKRLIS SVEDFTEFV*
Mutated AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKRIQTS LTSASLGSAD
ENSVAQADDS LKNLHLELTE TCLDMMARYV FSNFTAVPKR SPVGEFLLAG GRTKTWLVGN
KLVTVTTSVG TGTRSLLGLD SGELQSGPES SSSPGVHVRQ TKEAPAKLES QAGQQVSRGA
RDRVRSMSGG HGLRVGALDV PASQFLGSAT SPGPRTAPAA KPEKASAGTR VPVQEKTNLA
AYVPLLTQGW AEILVRRPTG NTSWLMSLEN PLSPFSSDIN NMPLQELSNA LMAAERFKEH
RDTALYKSLS VPAASTAKPP PLPRSNTDSA VVMEEGSPGE VPVLVEPPGL EDVEAALGMD
RRTDAYSRSS SVSSQEEKSL HAEELVGRGI PIERVVSSEG GRPSVDLSFQ PSQPLSKSSS
SPEL*
Position of stopcodon in wt / mu CDS 5310 / 3975
Position (AA) of stopcodon in wt / mu AA sequence 1770 / 1325
Position of stopcodon in wt / mu cDNA 5372 / 4037
Position of start ATG in wt / mu cDNA 63 / 63
Last intron/exon boundary 5207
Theoretical NMD boundary in CDS 5094
Length of CDS 5310
Coding sequence (CDS) position 3973
cDNA position 4035
gDNA position 36430
Chromosomal position 2084396
Speed 0.12 s

All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project

Back to summary table

Yum, tasty mutations...

MutationT@ster 2025

Variant:

16:2084396C>T_10_ENST00000439673

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr16:2084396C>T (GRCh38)
Gene symbol TSC2
Gene constraints LOEUF: 0.17, LOF (oe): 0.12, misssense (oe): 0.98, synonymous (oe): 1.27 ? (gnomAD)
Ensembl transcript ID ENST00000439673.6
Genbank transcript ID NM_001406693 (by similarity), NM_001318827 (by similarity), NM_001406678 (by similarity), NM_001406685 (by similarity), NM_001406688 (by similarity)
UniProt / AlphaMissense peptide TSC2_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.3865C>T
g.36430C>T
AA changes Q1289* Score: 6.0?
Frameshift No
Length of protein NMD
Pathogenic variant (ClinVar)
Tuberous sclerosis syndrome
Tuberous sclerosis 2
See cases
pathogenicClinVar OMIM
Variant DBs
Not in dbSNP
Allele 'T' was not found in gnomAD
Protein conservation
SpeciesMatchGeneAAAlignment
Human      1289PLSKSSSSPELQTLQDILGDPGDK
mutated  no alignment    n/a
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
Protein features
Start (aa)End (aa)FeatureDetails 
11807CHAINlost
13311352REGIONlost
13371337MOD_RESPhosphoserinelost
13381338MOD_RESPhosphoserinelost
13461346MOD_RESPhosphoserinelost
13641364MOD_RESPhosphoserinelost
13641488REGIONlost
13701394COMPBIASPolar residueslost
13871387MOD_RESPhosphoserinelost
14111411MOD_RESPhosphoserinelost
14181418MOD_RESPhosphoserinelost
14201420MOD_RESPhosphoserinelost
14521452MOD_RESPhosphoserinelost
14621462MOD_RESPhosphothreoninelost
14691484COMPBIASBasic and acidic residueslost
15311758DOMAINRap-GAPlost
17641764MOD_RESPhosphoserinelost
17651793REGIONlost
17981798MOD_RESPhosphoserinelost
17991799MOD_RESPhosphoserinelost
Phylogenetic conservation
PhyloPPhastCons
(flanking)-0.9380.04
5.7081
(flanking)6.7391
?
Splice sites No abrogation of potential splice sites predicted by MaxEntScan.
Distance from splice site N/A
Kozak consensus sequence altered? No
poly(A) signal N/A
AA sequence altered Yes
Chromosome 16
Strand 1
Original gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Original cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Wildtype AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEGERLG VLRALFFKVI KDYPSNEDLH ERLEVFKALT DNGRHITYLE
EELADFVLQW MDVGLSSEFL LVLVNLVKFN SCYLDEYIAR MVQMICLLCV RTASSVDIEV
SLQVLDAVVC YNCLPAESLP LFIVTLCRTI NVKELCEPCW KLMRNLLGTH LGHSAIYNMC
HLMEDRAYME DAPLLRGAVF FVGMALWGAH RLYSLRNSPT SVLPSFYQAM ACPNEVVSYE
IVLSITRLIK KYRKELQVVA WDILLNIIER LLQQLQTLDS PELRTIVHDL LTTVEELCDQ
NEFHGSQERY FELVERCADQ RPESSLLNLI SYRAQSIHPA KDGWIQNLQA LMERFFRSES
RGAVRIKVLD VLSFVLLINR QFYEEELINS VVISQLSHIP EDKDHQVRKL ATQLLVDLAE
GCHTHHFNSL LDIIEKVMAR SLSPPPELEE RDVAAYSASL EDVKTAVLGL LVILQTKLYT
LPASHATRVY EMLVSHIQLH YKHSYTLPIA SSIRLQAFDF LLLLRADSLH RLGLPNKDGV
VRFSPYCVCD YMEPERGSEK KTSGPLSPPT GPPGPAPAGP AVRLGSVPYS LLFRVLLQCL
KQESDWKVLK LVLGRLPESL RYKVLIFTSP CSVDQLCSAL CSMLSGPKTL ERLRGAPEGF
SRTDLHLAVV PVLTALISYH NYLDKTKQRE MVYCLEQGLI HRCASQCVVA LSICSVEMPD
IIIKALPVLV VKLTHISATA SMAVPLLEFL STLARLPHLY RNFAAEQYAS VFAISLPYTN
PSKFNQYIVC LAHHVIAMWF IRCRLPFRKD FVPFITKGLR SNVLLSFDDT PEKDSFRARS
TSLNERPKSR IQTSLTSASL GSADENSVAQ ADDSLKNLHL ELTETCLDMM ARYVFSNFTA
VPKRSPVGEF LLAGGRTKTW LVGNKLVTVT TSVGTGTRSL LGLDSGELQS GPESSSSPGV
HVRQTKEAPA KLESQAGQQV SRGARDRVRS MSGGHGLRVG ALDVPASQFL GSATSPGPRT
APAAKPEKAS AGTRVPVQEK TNLAAYVPLL TQGWAEILVR RPTGNTSWLM SLENPLSPFS
SDINNMPLQE LSNALMAAER FKEHRDTALY KSLSVPAAST AKPPPLPRSN TDSAVVMEEG
SPGEVPVLVE PPGLEDVEAA LGMDRRTDAY SRSSSVSSQE EKSLHAEELV GRGIPIERVV
SSEGGRPSVD LSFQPSQPLS KSSSSPELQT LQDILGDPGD KADVGRLSPE VKARSQSGTL
DGESAAWSAS GEDSRGQPEG PLPSSSPRSP SGLRPRGYTI SDSAPSRRGK RVERDALKSR
ATASNAEKVP GINPSFVFLQ LYHSPFFGDE SNKPILLPNE SQSFERSVQL LDQIPSYDTH
KIAVLYVGEG QSNSELAILS NEHGSYRYTE FLTGLGRLIE LKDCQPDKVY LGGLDVCGED
GQFTYCWHDD IMQAVFHIAT LMPTKDVDKH RCDKKRHLGN DFVSIVYNDS GEDFKLGTIK
GQFNFVHVIV TPLDYECNLV SLQCRKDMEG LVDTSVAKIV SDRNLPFVAR QMALHANMAS
QVHHSRSNPT DIYPSKWIAR LRHIKRLRQR ICEEAAYSNP SLPLVHPPSH SKAPAQTPAE
PTPGYEVGQR KRLISSVEDF TEFV*
Mutated AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEGERLG VLRALFFKVI KDYPSNEDLH ERLEVFKALT DNGRHITYLE
EELADFVLQW MDVGLSSEFL LVLVNLVKFN SCYLDEYIAR MVQMICLLCV RTASSVDIEV
SLQVLDAVVC YNCLPAESLP LFIVTLCRTI NVKELCEPCW KLMRNLLGTH LGHSAIYNMC
HLMEDRAYME DAPLLRGAVF FVGMALWGAH RLYSLRNSPT SVLPSFYQAM ACPNEVVSYE
IVLSITRLIK KYRKELQVVA WDILLNIIER LLQQLQTLDS PELRTIVHDL LTTVEELCDQ
NEFHGSQERY FELVERCADQ RPESSLLNLI SYRAQSIHPA KDGWIQNLQA LMERFFRSES
RGAVRIKVLD VLSFVLLINR QFYEEELINS VVISQLSHIP EDKDHQVRKL ATQLLVDLAE
GCHTHHFNSL LDIIEKVMAR SLSPPPELEE RDVAAYSASL EDVKTAVLGL LVILQTKLYT
LPASHATRVY EMLVSHIQLH YKHSYTLPIA SSIRLQAFDF LLLLRADSLH RLGLPNKDGV
VRFSPYCVCD YMEPERGSEK KTSGPLSPPT GPPGPAPAGP AVRLGSVPYS LLFRVLLQCL
KQESDWKVLK LVLGRLPESL RYKVLIFTSP CSVDQLCSAL CSMLSGPKTL ERLRGAPEGF
SRTDLHLAVV PVLTALISYH NYLDKTKQRE MVYCLEQGLI HRCASQCVVA LSICSVEMPD
IIIKALPVLV VKLTHISATA SMAVPLLEFL STLARLPHLY RNFAAEQYAS VFAISLPYTN
PSKFNQYIVC LAHHVIAMWF IRCRLPFRKD FVPFITKGLR SNVLLSFDDT PEKDSFRARS
TSLNERPKSR IQTSLTSASL GSADENSVAQ ADDSLKNLHL ELTETCLDMM ARYVFSNFTA
VPKRSPVGEF LLAGGRTKTW LVGNKLVTVT TSVGTGTRSL LGLDSGELQS GPESSSSPGV
HVRQTKEAPA KLESQAGQQV SRGARDRVRS MSGGHGLRVG ALDVPASQFL GSATSPGPRT
APAAKPEKAS AGTRVPVQEK TNLAAYVPLL TQGWAEILVR RPTGNTSWLM SLENPLSPFS
SDINNMPLQE LSNALMAAER FKEHRDTALY KSLSVPAAST AKPPPLPRSN TDSAVVMEEG
SPGEVPVLVE PPGLEDVEAA LGMDRRTDAY SRSSSVSSQE EKSLHAEELV GRGIPIERVV
SSEGGRPSVD LSFQPSQPLS KSSSSPEL*
Position of stopcodon in wt / mu CDS 5115 / 3867
Position (AA) of stopcodon in wt / mu AA sequence 1705 / 1289
Position of stopcodon in wt / mu cDNA 5196 / 3948
Position of start ATG in wt / mu cDNA 82 / 82
Last intron/exon boundary 5031
Theoretical NMD boundary in CDS 4899
Length of CDS 5115
Coding sequence (CDS) position 3865
cDNA position 3946
gDNA position 36430
Chromosomal position 2084396
Speed 0.10 s

All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project

Back to summary table

Yum, tasty mutations...

MutationT@ster 2025

Variant:

16:2084396C>T_14_ENST00000642797

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr16:2084396C>T (GRCh38)
Gene symbol TSC2
Gene constraints LOEUF: 0.17, LOF (oe): 0.12, misssense (oe): 0.98, synonymous (oe): 1.28 ? (gnomAD)
Ensembl transcript ID ENST00000642797.1
Genbank transcript ID NM_001363528 (by similarity), NM_001406671 (by similarity)
UniProt / AlphaMissense peptide N/A
Variant type Single base exchange
Gene region CDS
DNA changes c.3976C>T
g.36430C>T
AA changes Q1326* Score: 6.0?
Frameshift No
Length of protein NMD
Pathogenic variant (ClinVar)
Tuberous sclerosis syndrome
Tuberous sclerosis 2
See cases
pathogenicClinVar OMIM
Variant DBs
Not in dbSNP
Allele 'T' was not found in gnomAD
Protein conservation
SpeciesMatchGeneAAAlignment
Human      1326PLSKSSSSPELQTLQDILGDPGDK
mutated  no alignment    n/a
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
Protein features N/A
Phylogenetic conservation
PhyloPPhastCons
(flanking)-0.9380.04
5.7081
(flanking)6.7391
?
Splice sites No abrogation of potential splice sites predicted by MaxEntScan.
Distance from splice site N/A
Kozak consensus sequence altered? No
poly(A) signal N/A
AA sequence altered Yes
Chromosome 16
Strand 1
Original gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Original cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Wildtype AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSRIQT SLTSASLGSA
DENSVAQADD SLKNLHLELT ETCLDMMARY VFSNFTAVPK RSPVGEFLLA GGRTKTWLVG
NKLVTVTTSV GTGTRSLLGL DSGELQSGPE SSSSPGVHVR QTKEAPAKLE SQAGQQVSRG
ARDRVRSMSG GHGLRVGALD VPASQFLGSA TSPGPRTAPA AKPEKASAGT RVPVQEKTNL
AAYVPLLTQG WAEILVRRPT GNTSWLMSLE NPLSPFSSDI NNMPLQELSN ALMAAERFKE
HRDTALYKSL SVPAASTAKP PPLPRSNTDS AVVMEEGSPG EVPVLVEPPG LEDVEAALGM
DRRTDAYSRS SSVSSQEEKS LHAEELVGRG IPIERVVSSE GGRPSVDLSF QPSQPLSKSS
SSPELQTLQD ILGDPGDKAD VGRLSPEVKA RSQSGTLDGE SAAWSASGED SRGQPEGPLP
SSSPRSPSGL RPRGYTISDS APSRRGKRVE RDALKSRATA SNAEKVPGIN PSFVFLQLYH
SPFFGDESNK PILLPNESQS FERSVQLLDQ IPSYDTHKIA VLYVGEGQSN SELAILSNEH
GSYRYTEFLT GLGRLIELKD CQPDKVYLGG LDVCGEDGQF TYCWHDDIMQ AVFHIATLMP
TKDVDKHRCD KKRHLGNDFV SIVYNDSGED FKLGTIKGQF NFVHVIVTPL DYECNLVSLQ
CRKDMEGLVD TSVAKIVSDR NLPFVARQMA LHANMASQVH HSRSNPTDIY PSKWIARLRH
IKRLRQRICE EAAYSNPSLP LVHPPSHSKA PAQTPAEPTP GYEVGQRKRL ISSVEDFTEF
V*
Mutated AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSRIQT SLTSASLGSA
DENSVAQADD SLKNLHLELT ETCLDMMARY VFSNFTAVPK RSPVGEFLLA GGRTKTWLVG
NKLVTVTTSV GTGTRSLLGL DSGELQSGPE SSSSPGVHVR QTKEAPAKLE SQAGQQVSRG
ARDRVRSMSG GHGLRVGALD VPASQFLGSA TSPGPRTAPA AKPEKASAGT RVPVQEKTNL
AAYVPLLTQG WAEILVRRPT GNTSWLMSLE NPLSPFSSDI NNMPLQELSN ALMAAERFKE
HRDTALYKSL SVPAASTAKP PPLPRSNTDS AVVMEEGSPG EVPVLVEPPG LEDVEAALGM
DRRTDAYSRS SSVSSQEEKS LHAEELVGRG IPIERVVSSE GGRPSVDLSF QPSQPLSKSS
SSPEL*
Position of stopcodon in wt / mu CDS 5226 / 3978
Position (AA) of stopcodon in wt / mu AA sequence 1742 / 1326
Position of stopcodon in wt / mu cDNA 5280 / 4032
Position of start ATG in wt / mu cDNA 55 / 55
Last intron/exon boundary 5115
Theoretical NMD boundary in CDS 5010
Length of CDS 5226
Coding sequence (CDS) position 3976
cDNA position 4030
gDNA position 36430
Chromosomal position 2084396
Speed 0.10 s

All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project

Back to summary table

Yum, tasty mutations...

MutationT@ster 2025

Variant:

16:2084396C>T_11_ENST00000350773

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr16:2084396C>T (GRCh38)
Gene symbol TSC2
Gene constraints LOEUF: 0.17, LOF (oe): 0.12, misssense (oe): 0.99, synonymous (oe): 1.28 ? (gnomAD)
Ensembl transcript ID ENST00000350773.9
Genbank transcript ID NM_001406683 (by similarity), NM_001406689 (by similarity), NM_001114382 (by similarity), NM_001406664 (by similarity), NM_001406670 (by similarity), NM_001406682 (by similarity)
UniProt / AlphaMissense peptide TSC2_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.4105C>T
g.36430C>T
AA changes Q1369* Score: 6.0?
Frameshift No
Length of protein NMD
Pathogenic variant (ClinVar)
Tuberous sclerosis syndrome
Tuberous sclerosis 2
See cases
pathogenicClinVar OMIM
Variant DBs
Not in dbSNP
Allele 'T' was not found in gnomAD
Protein conservation
SpeciesMatchGeneAAAlignment
Human      1369PLSKSSSSPELQTLQDILGDPGDK
mutated  no alignment    n/a
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
Protein features
Start (aa)End (aa)FeatureDetails 
11807CHAINlost
13641488REGIONlost
13701394COMPBIASPolar residueslost
13871387MOD_RESPhosphoserinelost
14111411MOD_RESPhosphoserinelost
14181418MOD_RESPhosphoserinelost
14201420MOD_RESPhosphoserinelost
14521452MOD_RESPhosphoserinelost
14621462MOD_RESPhosphothreoninelost
14691484COMPBIASBasic and acidic residueslost
15311758DOMAINRap-GAPlost
17641764MOD_RESPhosphoserinelost
17651793REGIONlost
17981798MOD_RESPhosphoserinelost
17991799MOD_RESPhosphoserinelost
Phylogenetic conservation
PhyloPPhastCons
(flanking)-0.9380.04
5.7081
(flanking)6.7391
?
Splice sites No abrogation of potential splice sites predicted by MaxEntScan.
Distance from splice site N/A
Kozak consensus sequence altered? No
poly(A) signal N/A
AA sequence altered Yes
Chromosome 16
Strand 1
Original gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Original cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Wildtype AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSLRIA RPPKQGLNNS
PPVKEFKESS AAEAFRCRSI SVSEHVVRSR IQTSLTSASL GSADENSVAQ ADDSLKNLHL
ELTETCLDMM ARYVFSNFTA VPKRSPVGEF LLAGGRTKTW LVGNKLVTVT TSVGTGTRSL
LGLDSGELQS GPESSSSPGV HVRQTKEAPA KLESQAGQQV SRGARDRVRS MSGGHGLRVG
ALDVPASQFL GSATSPGPRT APAAKPEKAS AGTRVPVQEK TNLAAYVPLL TQGWAEILVR
RPTGNTSWLM SLENPLSPFS SDINNMPLQE LSNALMAAER FKEHRDTALY KSLSVPAAST
AKPPPLPRSN TDSAVVMEEG SPGEVPVLVE PPGLEDVEAA LGMDRRTDAY SRSSSVSSQE
EKSLHAEELV GRGIPIERVV SSEGGRPSVD LSFQPSQPLS KSSSSPELQT LQDILGDPGD
KADVGRLSPE VKARSQSGTL DGESAAWSAS GEDSRGQPEG PLPSSSPRSP SGLRPRGYTI
SDSAPSRRGK RVERDALKSR ATASNAEKVP GINPSFVFLQ LYHSPFFGDE SNKPILLPNE
SQSFERSVQL LDQIPSYDTH KIAVLYVGEG QSNSELAILS NEHGSYRYTE FLTGLGRLIE
LKDCQPDKVY LGGLDVCGED GQFTYCWHDD IMQAVFHIAT LMPTKDVDKH RCDKKRHLGN
DFVSIVYNDS GEDFKLGTIK GQFNFVHVIV TPLDYECNLV SLQCRKDMEG LVDTSVAKIV
SDRNLPFVAR QMALHANMAS QVHHSRSNPT DIYPSKWIAR LRHIKRLRQR ICEEAAYSNP
SLPLVHPPSH SKAPAQTPAE PTPGYEVGQR KRLISSVEDF TEFV*
Mutated AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSLRIA RPPKQGLNNS
PPVKEFKESS AAEAFRCRSI SVSEHVVRSR IQTSLTSASL GSADENSVAQ ADDSLKNLHL
ELTETCLDMM ARYVFSNFTA VPKRSPVGEF LLAGGRTKTW LVGNKLVTVT TSVGTGTRSL
LGLDSGELQS GPESSSSPGV HVRQTKEAPA KLESQAGQQV SRGARDRVRS MSGGHGLRVG
ALDVPASQFL GSATSPGPRT APAAKPEKAS AGTRVPVQEK TNLAAYVPLL TQGWAEILVR
RPTGNTSWLM SLENPLSPFS SDINNMPLQE LSNALMAAER FKEHRDTALY KSLSVPAAST
AKPPPLPRSN TDSAVVMEEG SPGEVPVLVE PPGLEDVEAA LGMDRRTDAY SRSSSVSSQE
EKSLHAEELV GRGIPIERVV SSEGGRPSVD LSFQPSQPLS KSSSSPEL*
Position of stopcodon in wt / mu CDS 5355 / 4107
Position (AA) of stopcodon in wt / mu AA sequence 1785 / 1369
Position of stopcodon in wt / mu cDNA 5430 / 4182
Position of start ATG in wt / mu cDNA 76 / 76
Last intron/exon boundary 5265
Theoretical NMD boundary in CDS 5139
Length of CDS 5355
Coding sequence (CDS) position 4105
cDNA position 4180
gDNA position 36430
Chromosomal position 2084396
Speed 0.12 s

All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project

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Yum, tasty mutations...

MutationT@ster 2025

Variant:

16:2084396C>T_16_ENST00000642561

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr16:2084396C>T (GRCh38)
Gene symbol TSC2
Gene constraints LOEUF: 0.21, LOF (oe): 0.15, misssense (oe): 0.98, synonymous (oe): 1.28 ? (gnomAD)
Ensembl transcript ID ENST00000642561.1
Genbank transcript ID NM_001370405 (by similarity)
UniProt / AlphaMissense peptide N/A
Variant type Single base exchange
Gene region CDS
DNA changes c.4045C>T
g.36430C>T
AA changes Q1349* Score: 6.0?
Frameshift No
Length of protein NMD
Pathogenic variant (ClinVar)
Tuberous sclerosis syndrome
Tuberous sclerosis 2
See cases
pathogenicClinVar OMIM
Variant DBs
Not in dbSNP
Allele 'T' was not found in gnomAD
Protein conservation
SpeciesMatchGeneAAAlignment
Human      1349PLSKSSSSPELQTLQDILGDPGDK
mutated  no alignment    n/a
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
Protein features N/A
Phylogenetic conservation
PhyloPPhastCons
(flanking)-0.9380.04
5.7081
(flanking)6.7391
?
Splice sites No abrogation of potential splice sites predicted by MaxEntScan.
Distance from splice site N/A
Kozak consensus sequence altered? No
poly(A) signal N/A
AA sequence altered Yes
Chromosome 16
Strand 1
Original gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Original cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Wildtype AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSRIQT SLTSASLGSA
DENSVAQADD SLKNLHLELT ETCLDMMARY VFSNFTAVPK RSPVGEFLLA GGRTKTWLVG
NKLVTVTTSV GTGTRSLLGL DSGELQSGPE SSSSPGVHVR QTKEAPAKLE SQAGQQVSRG
ARDRVRSMSG GHGLRVGALD VPASQFLGSA TSPGPRTAPA AKPEKASAGT RVPVQEKTNL
AAYVPLLTQG WAEILVRRPT GNTSWLMSLE NPLSPFSSDI NNMPLQELSN ALMAAERFKE
HRDTALYKSL SVPAASTAKP PPLPRSNTVA SFSSLYQSSC QGQLHRSVSW ADSAVVMEEG
SPGEVPVLVE PPGLEDVEAA LGMDRRTDAY SRSSSVSSQE EKSLHAEELV GRGIPIERVV
SSEGGRPSVD LSFQPSQPLS KSSSSPELQT LQDILGDPGD KADVGRLSPE VKARSQSGTL
DGESAAWSAS GEDSRGQPEG PLPSSSPRSP SGLRPRGYTI SDSAPSRRGK RVERDALKSR
ATASNAEKVP GINPSFVFLQ LYHSPFFGDE SNKPILLPNE SQSFERSVQL LDQIPSYDTH
KIAVLYVGEG QSNSELAILS NEHGSYRYTE FLTGLGRLIE LKDCQPDKVY LGGLDVCGED
GQFTYCWHDD IMQAVFHIAT LMPTKDVDKH RCDKKRHLGN DFVSIVYNDS GEDFKLGTIK
GQFNFVHVIV TPLDYECNLV SLQCRKDMEG LVDTSVAKIV SDRNLPFVAR QMALHANVHH
SRSNPTDIYP SKWIARLRHI KRLRQRICEE AAYSNPSLPL VHPPSHSKAP AQTPAEPTPG
YEVGQRKRLI SSVEDFTEFV *
Mutated AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSRIQT SLTSASLGSA
DENSVAQADD SLKNLHLELT ETCLDMMARY VFSNFTAVPK RSPVGEFLLA GGRTKTWLVG
NKLVTVTTSV GTGTRSLLGL DSGELQSGPE SSSSPGVHVR QTKEAPAKLE SQAGQQVSRG
ARDRVRSMSG GHGLRVGALD VPASQFLGSA TSPGPRTAPA AKPEKASAGT RVPVQEKTNL
AAYVPLLTQG WAEILVRRPT GNTSWLMSLE NPLSPFSSDI NNMPLQELSN ALMAAERFKE
HRDTALYKSL SVPAASTAKP PPLPRSNTVA SFSSLYQSSC QGQLHRSVSW ADSAVVMEEG
SPGEVPVLVE PPGLEDVEAA LGMDRRTDAY SRSSSVSSQE EKSLHAEELV GRGIPIERVV
SSEGGRPSVD LSFQPSQPLS KSSSSPEL*
Position of stopcodon in wt / mu CDS 5283 / 4047
Position (AA) of stopcodon in wt / mu AA sequence 1761 / 1349
Position of stopcodon in wt / mu cDNA 5335 / 4099
Position of start ATG in wt / mu cDNA 53 / 53
Last intron/exon boundary 5170
Theoretical NMD boundary in CDS 5067
Length of CDS 5283
Coding sequence (CDS) position 4045
cDNA position 4097
gDNA position 36430
Chromosomal position 2084396
Speed 0.12 s

All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project

Back to summary table

Yum, tasty mutations...

MutationT@ster 2025

Variant:

16:2084396C>T_17_ENST00000568454

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr16:2084396C>T (GRCh38)
Gene symbol TSC2
Gene constraints LOEUF: 0.18, LOF (oe): 0.13, misssense (oe): 0.98, synonymous (oe): 1.28 ? (gnomAD)
Ensembl transcript ID ENST00000568454.6
Genbank transcript ID NM_001318832 (by similarity)
UniProt / AlphaMissense peptide N/A
Variant type Single base exchange
Gene region CDS
DNA changes c.4006C>T
g.36430C>T
AA changes Q1336* Score: 6.0?
Frameshift No
Length of protein NMD
Pathogenic variant (ClinVar)
Tuberous sclerosis syndrome
Tuberous sclerosis 2
See cases
pathogenicClinVar OMIM
Variant DBs
Not in dbSNP
Allele 'T' was not found in gnomAD
Protein conservation
SpeciesMatchGeneAAAlignment
Human      1336PLSKSSSSPELQTLQDILGDPGDK
mutated  no alignment    n/a
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
Protein features N/A
Phylogenetic conservation
PhyloPPhastCons
(flanking)-0.9380.04
5.7081
(flanking)6.7391
?
Splice sites No abrogation of potential splice sites predicted by MaxEntScan.
Distance from splice site N/A
Kozak consensus sequence altered? No
poly(A) signal N/A
AA sequence altered Yes
Chromosome 16
Strand 1
Original gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Original cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Wildtype AA sequence MEGFSGASWS TMAKPTSKDS GLKEKFKILL GLGTPRPNPR SAEGKQTEFI ITAEILRELS
MECGLNNRIR MIGQICEVAK TKKFEEHAVE ALWKAVADLL QPERPLEARH AVLALLKAIV
QGQGERLGVL RALFFKVIKD YPSNEDLHER LEVFKALTDN GRHITYLEEE LADFVLQWMD
VGLSSEFLLV LVNLVKFNSC YLDEYIARMV QMICLLCVRT ASSVDIEVSL QVLDAVVCYN
CLPAESLPLF IVTLCRTINV KELCEPCWKL MRNLLGTHLG HSAIYNMCHL MEDRAYMEDA
PLLRGAVFFV GMALWGAHRL YSLRNSPTSV LPSFYQAMAC PNEVVSYEIV LSITRLIKKY
RKELQVVAWD ILLNIIERLL QQLQTLDSPE LRTIVHDLLT TVEELCDQNE FHGSQERYFE
LVERCADQRP ESSLLNLISY RAQSIHPAKD GWIQNLQALM ERFFRSESRG AVRIKVLDVL
SFVLLINRQF YEEELINSVV ISQLSHIPED KDHQVRKLAT QLLVDLAEGC HTHHFNSLLD
IIEKVMARSL SPPPELEERD VAAYSASLED VKTAVLGLLV ILQTKLYTLP ASHATRVYEM
LVSHIQLHYK HSYTLPIASS IRLQAFDFLL LLRADSLHRL GLPNKDGVVR FSPYCVCDYM
EPERGSEKKT SGPLSPPTGP PGPAPAGPAV RLGSVPYSLL FRVLLQCLKQ ESDWKVLKLV
LGRLPESLRY KVLIFTSPCS VDQLCSALCS MLSGPKTLER LRGAPEGFSR TDLHLAVVPV
LTALISYHNY LDKTKQREMV YCLEQGLIHR CASQCVVALS ICSVEMPDII IKALPVLVVK
LTHISATASM AVPLLEFLST LARLPHLYRN FAAEQYASVF AISLPYTNPS KFNQYIVCLA
HHVIAMWFIR CRLPFRKDFV PFITKGLRSN VLLSFDDTPE KDSFRARSTS LNERPKRIQT
SLTSASLGSA DENSVAQADD SLKNLHLELT ETCLDMMARY VFSNFTAVPK RSPVGEFLLA
GGRTKTWLVG NKLVTVTTSV GTGTRSLLGL DSGELQSGPE SSSSPGVHVR QTKEAPAKLE
SQAGQQVSRG ARDRVRSMSG GHGLRVGALD VPASQFLGSA TSPGPRTAPA AKPEKASAGT
RVPVQEKTNL AAYVPLLTQG WAEILVRRPT GNTSWLMSLE NPLSPFSSDI NNMPLQELSN
ALMAAERFKE HRDTALYKSL SVPAASTAKP PPLPRSNTDS AVVMEEGSPG EVPVLVEPPG
LEDVEAALGM DRRTDAYSRS SSVSSQEEKS LHAEELVGRG IPIERVVSSE GGRPSVDLSF
QPSQPLSKSS SSPELQTLQD ILGDPGDKAD VGRLSPEVKA RSQSGTLDGE SAAWSASGED
SRGQPEGPLP SSSPRSPSGL RPRGYTISDS APSRRGKRVE RDALKSRATA SNAEKVPGIN
PSFVFLQLYH SPFFGDESNK PILLPNESQS FERSVQLLDQ IPSYDTHKIA VLYVGEGQSN
SELAILSNEH GSYRYTEFLT GLGRLIELKD CQPDKVYLGG LDVCGEDGQF TYCWHDDIMQ
AVFHIATLMP TKDVDKHRCD KKRHLGNDFV SIVYNDSGED FKLGTIKGQF NFVHVIVTPL
DYECNLVSLQ CRKDMEGLVD TSVAKIVSDR NLPFVARQMA LHANMASQVH HSRSNPTDIY
PSKWIARLRH IKRLRQRICE EAAYSNPSLP LVHPPSHSKA PAQTPAEPTP GYEVGQRKRL
ISSVEDFTEF V*
Mutated AA sequence MEGFSGASWS TMAKPTSKDS GLKEKFKILL GLGTPRPNPR SAEGKQTEFI ITAEILRELS
MECGLNNRIR MIGQICEVAK TKKFEEHAVE ALWKAVADLL QPERPLEARH AVLALLKAIV
QGQGERLGVL RALFFKVIKD YPSNEDLHER LEVFKALTDN GRHITYLEEE LADFVLQWMD
VGLSSEFLLV LVNLVKFNSC YLDEYIARMV QMICLLCVRT ASSVDIEVSL QVLDAVVCYN
CLPAESLPLF IVTLCRTINV KELCEPCWKL MRNLLGTHLG HSAIYNMCHL MEDRAYMEDA
PLLRGAVFFV GMALWGAHRL YSLRNSPTSV LPSFYQAMAC PNEVVSYEIV LSITRLIKKY
RKELQVVAWD ILLNIIERLL QQLQTLDSPE LRTIVHDLLT TVEELCDQNE FHGSQERYFE
LVERCADQRP ESSLLNLISY RAQSIHPAKD GWIQNLQALM ERFFRSESRG AVRIKVLDVL
SFVLLINRQF YEEELINSVV ISQLSHIPED KDHQVRKLAT QLLVDLAEGC HTHHFNSLLD
IIEKVMARSL SPPPELEERD VAAYSASLED VKTAVLGLLV ILQTKLYTLP ASHATRVYEM
LVSHIQLHYK HSYTLPIASS IRLQAFDFLL LLRADSLHRL GLPNKDGVVR FSPYCVCDYM
EPERGSEKKT SGPLSPPTGP PGPAPAGPAV RLGSVPYSLL FRVLLQCLKQ ESDWKVLKLV
LGRLPESLRY KVLIFTSPCS VDQLCSALCS MLSGPKTLER LRGAPEGFSR TDLHLAVVPV
LTALISYHNY LDKTKQREMV YCLEQGLIHR CASQCVVALS ICSVEMPDII IKALPVLVVK
LTHISATASM AVPLLEFLST LARLPHLYRN FAAEQYASVF AISLPYTNPS KFNQYIVCLA
HHVIAMWFIR CRLPFRKDFV PFITKGLRSN VLLSFDDTPE KDSFRARSTS LNERPKRIQT
SLTSASLGSA DENSVAQADD SLKNLHLELT ETCLDMMARY VFSNFTAVPK RSPVGEFLLA
GGRTKTWLVG NKLVTVTTSV GTGTRSLLGL DSGELQSGPE SSSSPGVHVR QTKEAPAKLE
SQAGQQVSRG ARDRVRSMSG GHGLRVGALD VPASQFLGSA TSPGPRTAPA AKPEKASAGT
RVPVQEKTNL AAYVPLLTQG WAEILVRRPT GNTSWLMSLE NPLSPFSSDI NNMPLQELSN
ALMAAERFKE HRDTALYKSL SVPAASTAKP PPLPRSNTDS AVVMEEGSPG EVPVLVEPPG
LEDVEAALGM DRRTDAYSRS SSVSSQEEKS LHAEELVGRG IPIERVVSSE GGRPSVDLSF
QPSQPLSKSS SSPEL*
Position of stopcodon in wt / mu CDS 5256 / 4008
Position (AA) of stopcodon in wt / mu AA sequence 1752 / 1336
Position of stopcodon in wt / mu cDNA 5324 / 4076
Position of start ATG in wt / mu cDNA 69 / 69
Last intron/exon boundary 5159
Theoretical NMD boundary in CDS 5040
Length of CDS 5256
Coding sequence (CDS) position 4006
cDNA position 4074
gDNA position 36430
Chromosomal position 2084396
Speed 0.11 s

All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project

Back to summary table

Yum, tasty mutations...

MutationT@ster 2025

Variant:

16:2084396C>T_15_ENST00000644043

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr16:2084396C>T (GRCh38)
Gene symbol TSC2
Gene constraints LOEUF: 0.20, LOF (oe): 0.15, misssense (oe): 0.98, synonymous (oe): 1.28 ? (gnomAD)
Ensembl transcript ID ENST00000644043.1
Genbank transcript ID NM_001406690 (by similarity), NM_021055 (by similarity)
UniProt / AlphaMissense peptide TSC2_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.4045C>T
g.36430C>T
AA changes Q1349* Score: 6.0?
Frameshift No
Length of protein NMD
Pathogenic variant (ClinVar)
Tuberous sclerosis syndrome
Tuberous sclerosis 2
See cases
pathogenicClinVar OMIM
Variant DBs
Not in dbSNP
Allele 'T' was not found in gnomAD
Protein conservation
SpeciesMatchGeneAAAlignment
Human      1349PLSKSSSSPELQTLQDILGDPGDK
mutated  no alignment    n/a
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
Protein features
Start (aa)End (aa)FeatureDetails 
11807CHAINlost
13311352REGIONlost
13641364MOD_RESPhosphoserinelost
13641488REGIONlost
13701394COMPBIASPolar residueslost
13871387MOD_RESPhosphoserinelost
14111411MOD_RESPhosphoserinelost
14181418MOD_RESPhosphoserinelost
14201420MOD_RESPhosphoserinelost
14521452MOD_RESPhosphoserinelost
14621462MOD_RESPhosphothreoninelost
14691484COMPBIASBasic and acidic residueslost
15311758DOMAINRap-GAPlost
17641764MOD_RESPhosphoserinelost
17651793REGIONlost
17981798MOD_RESPhosphoserinelost
17991799MOD_RESPhosphoserinelost
Phylogenetic conservation
PhyloPPhastCons
(flanking)-0.9380.04
5.7081
(flanking)6.7391
?
Splice sites No abrogation of potential splice sites predicted by MaxEntScan.
Distance from splice site N/A
Kozak consensus sequence altered? No
poly(A) signal N/A
AA sequence altered Yes
Chromosome 16
Strand 1
Original gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Original cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Wildtype AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSRIQT SLTSASLGSA
DENSVAQADD SLKNLHLELT ETCLDMMARY VFSNFTAVPK RSPVGEFLLA GGRTKTWLVG
NKLVTVTTSV GTGTRSLLGL DSGELQSGPE SSSSPGVHVR QTKEAPAKLE SQAGQQVSRG
ARDRVRSMSG GHGLRVGALD VPASQFLGSA TSPGPRTAPA AKPEKASAGT RVPVQEKTNL
AAYVPLLTQG WAEILVRRPT GNTSWLMSLE NPLSPFSSDI NNMPLQELSN ALMAAERFKE
HRDTALYKSL SVPAASTAKP PPLPRSNTVA SFSSLYQSSC QGQLHRSVSW ADSAVVMEEG
SPGEVPVLVE PPGLEDVEAA LGMDRRTDAY SRSSSVSSQE EKSLHAEELV GRGIPIERVV
SSEGGRPSVD LSFQPSQPLS KSSSSPELQT LQDILGDPGD KADVGRLSPE VKARSQSGTL
DGESAAWSAS GEDSRGQPEG PLPSSSPRSP SGLRPRGYTI SDSAPSRRGK RVERDALKSR
ATASNAEKVP GINPSFVFLQ LYHSPFFGDE SNKPILLPNE SQSFERSVQL LDQIPSYDTH
KIAVLYVGEG QSNSELAILS NEHGSYRYTE FLTGLGRLIE LKDCQPDKVY LGGLDVCGED
GQFTYCWHDD IMQAVFHIAT LMPTKDVDKH RCDKKRHLGN DFVSIVYNDS GEDFKLGTIK
GQFNFVHVIV TPLDYECNLV SLQCRKDMEG LVDTSVAKIV SDRNLPFVAR QMALHANMAS
QVHHSRSNPT DIYPSKWIAR LRHIKRLRQR ICEEAAYSNP SLPLVHPPSH SKAPAQTPAE
PTPGYEVGQR KRLISSVEDF TEFV*
Mutated AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKSRIQT SLTSASLGSA
DENSVAQADD SLKNLHLELT ETCLDMMARY VFSNFTAVPK RSPVGEFLLA GGRTKTWLVG
NKLVTVTTSV GTGTRSLLGL DSGELQSGPE SSSSPGVHVR QTKEAPAKLE SQAGQQVSRG
ARDRVRSMSG GHGLRVGALD VPASQFLGSA TSPGPRTAPA AKPEKASAGT RVPVQEKTNL
AAYVPLLTQG WAEILVRRPT GNTSWLMSLE NPLSPFSSDI NNMPLQELSN ALMAAERFKE
HRDTALYKSL SVPAASTAKP PPLPRSNTVA SFSSLYQSSC QGQLHRSVSW ADSAVVMEEG
SPGEVPVLVE PPGLEDVEAA LGMDRRTDAY SRSSSVSSQE EKSLHAEELV GRGIPIERVV
SSEGGRPSVD LSFQPSQPLS KSSSSPEL*
Position of stopcodon in wt / mu CDS 5295 / 4047
Position (AA) of stopcodon in wt / mu AA sequence 1765 / 1349
Position of stopcodon in wt / mu cDNA 5349 / 4101
Position of start ATG in wt / mu cDNA 55 / 55
Last intron/exon boundary 5184
Theoretical NMD boundary in CDS 5079
Length of CDS 5295
Coding sequence (CDS) position 4045
cDNA position 4099
gDNA position 36430
Chromosomal position 2084396
Speed 0.11 s

All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project

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Yum, tasty mutations...

MutationT@ster 2025

Variant:

16:2084396C>T_18_ENST00000642936

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Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr16:2084396C>T (GRCh38)
Gene symbol TSC2
Gene constraints LOEUF: 0.21, LOF (oe): 0.15, misssense (oe): 0.98, synonymous (oe): 1.28 ? (gnomAD)
Ensembl transcript ID ENST00000642936.1
Genbank transcript ID NM_001406691 (by similarity), NM_001406665 (by similarity), NM_001370404 (by similarity), NM_001318831 (by similarity)
UniProt / AlphaMissense peptide TSC2_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.4042C>T
g.36430C>T
AA changes Q1348* Score: 6.0?
Frameshift No
Length of protein NMD
Pathogenic variant (ClinVar)
Tuberous sclerosis syndrome
Tuberous sclerosis 2
See cases
pathogenicClinVar OMIM
Variant DBs
Not in dbSNP
Allele 'T' was not found in gnomAD
Protein conservation
SpeciesMatchGeneAAAlignment
Human      1348PLSKSSSSPELQTLQDILGDPGDK
mutated  no alignment    n/a
Ptroglodytes  no homologue    
Mmulatta  no homologue    
Fcatus  no homologue    
Mmusculus  no homologue    
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  no homologue    
Protein features
Start (aa)End (aa)FeatureDetails 
11807CHAINlost
13311352REGIONlost
13641364MOD_RESPhosphoserinelost
13641488REGIONlost
13701394COMPBIASPolar residueslost
13871387MOD_RESPhosphoserinelost
14111411MOD_RESPhosphoserinelost
14181418MOD_RESPhosphoserinelost
14201420MOD_RESPhosphoserinelost
14521452MOD_RESPhosphoserinelost
14621462MOD_RESPhosphothreoninelost
14691484COMPBIASBasic and acidic residueslost
15311758DOMAINRap-GAPlost
17641764MOD_RESPhosphoserinelost
17651793REGIONlost
17981798MOD_RESPhosphoserinelost
17991799MOD_RESPhosphoserinelost
Phylogenetic conservation
PhyloPPhastCons
(flanking)-0.9380.04
5.7081
(flanking)6.7391
?
Splice sites No abrogation of potential splice sites predicted by MaxEntScan.
Distance from splice site N/A
Kozak consensus sequence altered? No
poly(A) signal N/A
AA sequence altered Yes
Chromosome 16
Strand 1
Original gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered gDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Original cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGCAGACTCTGCAGGACATCCTC
Altered cDNA sequence snippet CCAGCTCCTCTCCCGAGCTGTAGACTCTGCAGGACATCCTC
Wildtype AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKRIQTS LTSASLGSAD
ENSVAQADDS LKNLHLELTE TCLDMMARYV FSNFTAVPKR SPVGEFLLAG GRTKTWLVGN
KLVTVTTSVG TGTRSLLGLD SGELQSGPES SSSPGVHVRQ TKEAPAKLES QAGQQVSRGA
RDRVRSMSGG HGLRVGALDV PASQFLGSAT SPGPRTAPAA KPEKASAGTR VPVQEKTNLA
AYVPLLTQGW AEILVRRPTG NTSWLMSLEN PLSPFSSDIN NMPLQELSNA LMAAERFKEH
RDTALYKSLS VPAASTAKPP PLPRSNTVAS FSSLYQSSCQ GQLHRSVSWA DSAVVMEEGS
PGEVPVLVEP PGLEDVEAAL GMDRRTDAYS RSSSVSSQEE KSLHAEELVG RGIPIERVVS
SEGGRPSVDL SFQPSQPLSK SSSSPELQTL QDILGDPGDK ADVGRLSPEV KARSQSGTLD
GESAAWSASG EDSRGQPEGP LPSSSPRSPS GLRPRGYTIS DSAPSRRGKR VERDALKSRA
TASNAEKVPG INPSFVFLQL YHSPFFGDES NKPILLPNES QSFERSVQLL DQIPSYDTHK
IAVLYVGEGQ SNSELAILSN EHGSYRYTEF LTGLGRLIEL KDCQPDKVYL GGLDVCGEDG
QFTYCWHDDI MQAVFHIATL MPTKDVDKHR CDKKRHLGND FVSIVYNDSG EDFKLGTIKG
QFNFVHVIVT PLDYECNLVS LQCRKDMEGL VDTSVAKIVS DRNLPFVARQ MALHANMASQ
VHHSRSNPTD IYPSKWIARL RHIKRLRQRI CEEAAYSNPS LPLVHPPSHS KAPAQTPAEP
TPGYEVGQRK RLISSVEDFT EFV*
Mutated AA sequence MAKPTSKDSG LKEKFKILLG LGTPRPNPRS AEGKQTEFII TAEILRELSM ECGLNNRIRM
IGQICEVAKT KKFEEHAVEA LWKAVADLLQ PERPLEARHA VLALLKAIVQ GQGERLGVLR
ALFFKVIKDY PSNEDLHERL EVFKALTDNG RHITYLEEEL ADFVLQWMDV GLSSEFLLVL
VNLVKFNSCY LDEYIARMVQ MICLLCVRTA SSVDIEVSLQ VLDAVVCYNC LPAESLPLFI
VTLCRTINVK ELCEPCWKLM RNLLGTHLGH SAIYNMCHLM EDRAYMEDAP LLRGAVFFVG
MALWGAHRLY SLRNSPTSVL PSFYQAMACP NEVVSYEIVL SITRLIKKYR KELQVVAWDI
LLNIIERLLQ QLQTLDSPEL RTIVHDLLTT VEELCDQNEF HGSQERYFEL VERCADQRPE
SSLLNLISYR AQSIHPAKDG WIQNLQALME RFFRSESRGA VRIKVLDVLS FVLLINRQFY
EEELINSVVI SQLSHIPEDK DHQVRKLATQ LLVDLAEGCH THHFNSLLDI IEKVMARSLS
PPPELEERDV AAYSASLEDV KTAVLGLLVI LQTKLYTLPA SHATRVYEML VSHIQLHYKH
SYTLPIASSI RLQAFDFLLL LRADSLHRLG LPNKDGVVRF SPYCVCDYME PERGSEKKTS
GPLSPPTGPP GPAPAGPAVR LGSVPYSLLF RVLLQCLKQE SDWKVLKLVL GRLPESLRYK
VLIFTSPCSV DQLCSALCSM LSGPKTLERL RGAPEGFSRT DLHLAVVPVL TALISYHNYL
DKTKQREMVY CLEQGLIHRC ASQCVVALSI CSVEMPDIII KALPVLVVKL THISATASMA
VPLLEFLSTL ARLPHLYRNF AAEQYASVFA ISLPYTNPSK FNQYIVCLAH HVIAMWFIRC
RLPFRKDFVP FITKGLRSNV LLSFDDTPEK DSFRARSTSL NERPKRIQTS LTSASLGSAD
ENSVAQADDS LKNLHLELTE TCLDMMARYV FSNFTAVPKR SPVGEFLLAG GRTKTWLVGN
KLVTVTTSVG TGTRSLLGLD SGELQSGPES SSSPGVHVRQ TKEAPAKLES QAGQQVSRGA
RDRVRSMSGG HGLRVGALDV PASQFLGSAT SPGPRTAPAA KPEKASAGTR VPVQEKTNLA
AYVPLLTQGW AEILVRRPTG NTSWLMSLEN PLSPFSSDIN NMPLQELSNA LMAAERFKEH
RDTALYKSLS VPAASTAKPP PLPRSNTVAS FSSLYQSSCQ GQLHRSVSWA DSAVVMEEGS
PGEVPVLVEP PGLEDVEAAL GMDRRTDAYS RSSSVSSQEE KSLHAEELVG RGIPIERVVS
SEGGRPSVDL SFQPSQPLSK SSSSPEL*
Position of stopcodon in wt / mu CDS 5292 / 4044
Position (AA) of stopcodon in wt / mu AA sequence 1764 / 1348
Position of stopcodon in wt / mu cDNA 5401 / 4153
Position of start ATG in wt / mu cDNA 110 / 110
Last intron/exon boundary 5236
Theoretical NMD boundary in CDS 5076
Length of CDS 5292
Coding sequence (CDS) position 4042
cDNA position 4151
gDNA position 36430
Chromosomal position 2084396
Speed 0.11 s

All positions are in basepairs (bp) if not explicitly stated differently. cDNA/gDNA/chromosomal position: Ins/del are shown as 'last normal base / first normal base'.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project

Back to summary table