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: ENST00000557933
Querying Taster for transcript #2: ENST00000455727
Querying Taster for transcript #3: ENST00000535915
Querying Taster for transcript #4: ENST00000545707
Querying Taster for transcript #5: ENST00000558518
Querying Taster for transcript #6: ENST00000560467
Querying Taster for transcript #7: ENST00000558013
Querying Taster for transcript #8: ENST00000252444
MT speed 2.46 s - this script 4.967438 s

Transcript summary:

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Yum, tasty mutations...

MutationT@ster 2025

Variant:

19:11113398T>C_3_ENST00000535915

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Prediction:

DeleteriousPermalink

Summary:

  • Model: simple_aae
  • Tree vote: 91|9 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr19:11113398T>C (GRCh38)
Gene symbol LDLR
Gene constraints LOEUF: 1.05, LOF (oe): 0.88, misssense (oe): 0.97, synonymous (oe): 1.00 ? (gnomAD)
Ensembl transcript ID ENST00000535915.5
Genbank transcript ID NM_001195799 (by similarity)
UniProt / AlphaMissense peptide LDLR_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.1184T>C
g.23981T>C
AA changes
AAE:V395A?
Score:64
Frameshift No
Length of protein Normal
Pathogenic variant (ClinVar)
Hypercholesterolemia, familial, 1
Cardiovascular phenotype
Familial hypercholesterolemia
pathogenicClinVar OMIM
Variant DBs
dbSNP IDrs779732323
gnomADhomozygous (C/C)heterozygousallele carriers
01313
Protein conservation
SpeciesMatchGeneAAAlignment
Human      395NLRNVVALDTEVASNRIYWSDLSQ
mutated  not conserved    395NLRNVVALDTEAASNRIYWSDLS
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 
22788TOPO_DOMExtracellularlost
22860CHAINlost
Phylogenetic conservation
PhyloPPhastCons
(flanking)2.0890.98
6.0611
(flanking)-0.0540.859
?
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 19
Strand 1
Original gDNA sequence snippet GGTCGCTCTGGACACGGAGGTGGCCAGCAATAGAATCTACT
Altered gDNA sequence snippet GGTCGCTCTGGACACGGAGGCGGCCAGCAATAGAATCTACT
Original cDNA sequence snippet GGTCGCTCTGGACACGGAGGTGGCCAGCAATAGAATCTACT
Altered cDNA sequence snippet GGTCGCTCTGGACACGGAGGCGGCCAGCAATAGAATCTACT
Wildtype AA sequence MGPWGWKLRW TVALLLAAAG TAVGDRCERN EFQCQDGKCI SYKWVCDGSA ECQDGSDESQ
ETCSPKTCSQ DEFRCHDGKC ISRQFVCDSD RDCLDGSDEA SCPVLTCGPA SFQCNSSTCI
PQLWACDNDP DCEDGSDEWP QRCRGLYVFQ GDSSPCSAFE FHCLSGECIH SSWRCDGGPD
CKDKSDEENC AVATCRPDEF QCSDGNCIHG SRQCDREYDC KDMSDEVGCV NVTLCEGPNK
FKCHSGECIT LDKVCNMARD CRDWSDEPIK ECGTNECLDN NGGCSHVCND LKIGYECLCP
DGFQLVAQRR CEDIDECQDP DTCSQLCVNL EGGYKCQCEE GFQLDPHTKA CKAVGSIAYL
FFTNRHEVRK MTLDRSEYTS LIPNLRNVVA LDTEVASNRI YWSDLSQRMI CSTQLDRAHG
VSSYDTVISR DIQAPDGLAV DWIHSNIYWT DSVLGTVSVA DTKGVKRKTL FRENGSKPRA
IVVDPVHGFM YWTDWGTPAK IKKGGLNGVD IYSLVTENIQ WPNGITLDLL SGRLYWVDSK
LHSISSIDVN GGNRKTILED EKRLAHPFSL AVFEDKVFWT DIINEAIFSA NRLTGSDVNL
LAENLLSPED MVLFHNLTQP RGVNWCERTT LSNGGCQYLC LPAPQINPHS PKFTCACPDG
MLLARDMRSC LTEAEAAVAT QETSTVRLKV SSTAVRTQHT TTRPVPDTSR LPGATPGLTT
VEIVTMSHQA LGDVAGRGNE KKPSSVRALS IVLPIVLLVF LCLGVFLLWK NWRLKNINSI
NFDNPVYQKT TEDEVHICHN QDGYSYPSRQ MVSLEDDVA*
Mutated AA sequence MGPWGWKLRW TVALLLAAAG TAVGDRCERN EFQCQDGKCI SYKWVCDGSA ECQDGSDESQ
ETCSPKTCSQ DEFRCHDGKC ISRQFVCDSD RDCLDGSDEA SCPVLTCGPA SFQCNSSTCI
PQLWACDNDP DCEDGSDEWP QRCRGLYVFQ GDSSPCSAFE FHCLSGECIH SSWRCDGGPD
CKDKSDEENC AVATCRPDEF QCSDGNCIHG SRQCDREYDC KDMSDEVGCV NVTLCEGPNK
FKCHSGECIT LDKVCNMARD CRDWSDEPIK ECGTNECLDN NGGCSHVCND LKIGYECLCP
DGFQLVAQRR CEDIDECQDP DTCSQLCVNL EGGYKCQCEE GFQLDPHTKA CKAVGSIAYL
FFTNRHEVRK MTLDRSEYTS LIPNLRNVVA LDTEAASNRI YWSDLSQRMI CSTQLDRAHG
VSSYDTVISR DIQAPDGLAV DWIHSNIYWT DSVLGTVSVA DTKGVKRKTL FRENGSKPRA
IVVDPVHGFM YWTDWGTPAK IKKGGLNGVD IYSLVTENIQ WPNGITLDLL SGRLYWVDSK
LHSISSIDVN GGNRKTILED EKRLAHPFSL AVFEDKVFWT DIINEAIFSA NRLTGSDVNL
LAENLLSPED MVLFHNLTQP RGVNWCERTT LSNGGCQYLC LPAPQINPHS PKFTCACPDG
MLLARDMRSC LTEAEAAVAT QETSTVRLKV SSTAVRTQHT TTRPVPDTSR LPGATPGLTT
VEIVTMSHQA LGDVAGRGNE KKPSSVRALS IVLPIVLLVF LCLGVFLLWK NWRLKNINSI
NFDNPVYQKT TEDEVHICHN QDGYSYPSRQ MVSLEDDVA*
Position of stopcodon in wt / mu CDS 2460 / 2460
Position (AA) of stopcodon in wt / mu AA sequence 820 / 820
Position of stopcodon in wt / mu cDNA 2546 / 2546
Position of start ATG in wt / mu cDNA 87 / 87
Last intron/exon boundary 2510
Theoretical NMD boundary in CDS 2373
Length of CDS 2460
Coding sequence (CDS) position 1184
cDNA position 1270
gDNA position 23981
Chromosomal position 11113398
Speed 0.35 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:

19:11113398T>C_4_ENST00000545707

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: simple_aae
  • Tree vote: 94|6 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr19:11113398T>C (GRCh38)
Gene symbol LDLR
Gene constraints LOEUF: 1.07, LOF (oe): 0.89, misssense (oe): 0.95, synonymous (oe): 0.94 ? (gnomAD)
Ensembl transcript ID ENST00000545707.5
Genbank transcript ID NM_001195803 (by similarity)
UniProt / AlphaMissense peptide LDLR_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.926T>C
g.23981T>C
AA changes
AAE:V309A?
Score:64
Frameshift No
Length of protein Normal
Pathogenic variant (ClinVar)
Hypercholesterolemia, familial, 1
Cardiovascular phenotype
Familial hypercholesterolemia
pathogenicClinVar OMIM
Variant DBs
dbSNP IDrs779732323
gnomADhomozygous (C/C)heterozygousallele carriers
01313
Protein conservation
SpeciesMatchGeneAAAlignment
Human      309NLRNVVALDTEVASNRIYWSDLSQ
mutated  not conserved    309NVVALDTEAASNRIYWSDLS
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 
22788TOPO_DOMExtracellularlost
22860CHAINlost
274313DOMAINLDL-receptor class Alost
Phylogenetic conservation
PhyloPPhastCons
(flanking)2.0890.98
6.0611
(flanking)-0.0540.859
?
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 19
Strand 1
Original gDNA sequence snippet GGTCGCTCTGGACACGGAGGTGGCCAGCAATAGAATCTACT
Altered gDNA sequence snippet GGTCGCTCTGGACACGGAGGCGGCCAGCAATAGAATCTACT
Original cDNA sequence snippet GGTCGCTCTGGACACGGAGGTGGCCAGCAATAGAATCTACT
Altered cDNA sequence snippet GGTCGCTCTGGACACGGAGGCGGCCAGCAATAGAATCTACT
Wildtype AA sequence MGPWGWKLRW TVALLLAAAG TAVGDRCERN EFQCQDGKCI SYKWVCDGSA ECQDGSDESQ
ETCLSVTCKS GDFSCGGRVN RCIPQFWRCD GQVDCDNGSD EQGCPVATCR PDEFQCSDGN
CIHGSRQCDR EYDCKDMSDE VGCVNVTLCE GPNKFKCHSG ECITLDKVCN MARDCRDWSD
EPIKECGTNE CLDNNGGCSH VCNDLKIGYE CLCPDGFQLV AQRRCEDIDE CQDPDTCSQL
CVNLEGGYKC QCEEGFQLDP HTKACKAVGS IAYLFFTNRH EVRKMTLDRS EYTSLIPNLR
NVVALDTEVA SNRIYWSDLS QRMICSTQLD RAHGVSSYDT VISRDIQAPD GLAVDWIHSN
IYWTDSVLGT VSVADTKGVK RKTLFRENGS KPRAIVVDPV HGFMYWTDWG TPAKIKKGGL
NGVDIYSLVT ENIQWPNGIT LDLLSGRLYW VDSKLHSISS IDVNGGNRKT ILEDEKRLAH
PFSLAVFEDK VFWTDIINEA IFSANRLTGS DVNLLAENLL SPEDMVLFHN LTQPREAEAA
VATQETSTVR LKVSSTAVRT QHTTTRPVPD TSRLPGATPG LTTVEIVTMS HQALGDVAGR
GNEKKPSSVR ALSIVLPIVL LVFLCLGVFL LWKNWRLKNI NSINFDNPVY QKTTEDEVHI
CHNQDGYSYP SRQMVSLEDD VA*
Mutated AA sequence MGPWGWKLRW TVALLLAAAG TAVGDRCERN EFQCQDGKCI SYKWVCDGSA ECQDGSDESQ
ETCLSVTCKS GDFSCGGRVN RCIPQFWRCD GQVDCDNGSD EQGCPVATCR PDEFQCSDGN
CIHGSRQCDR EYDCKDMSDE VGCVNVTLCE GPNKFKCHSG ECITLDKVCN MARDCRDWSD
EPIKECGTNE CLDNNGGCSH VCNDLKIGYE CLCPDGFQLV AQRRCEDIDE CQDPDTCSQL
CVNLEGGYKC QCEEGFQLDP HTKACKAVGS IAYLFFTNRH EVRKMTLDRS EYTSLIPNLR
NVVALDTEAA SNRIYWSDLS QRMICSTQLD RAHGVSSYDT VISRDIQAPD GLAVDWIHSN
IYWTDSVLGT VSVADTKGVK RKTLFRENGS KPRAIVVDPV HGFMYWTDWG TPAKIKKGGL
NGVDIYSLVT ENIQWPNGIT LDLLSGRLYW VDSKLHSISS IDVNGGNRKT ILEDEKRLAH
PFSLAVFEDK VFWTDIINEA IFSANRLTGS DVNLLAENLL SPEDMVLFHN LTQPREAEAA
VATQETSTVR LKVSSTAVRT QHTTTRPVPD TSRLPGATPG LTTVEIVTMS HQALGDVAGR
GNEKKPSSVR ALSIVLPIVL LVFLCLGVFL LWKNWRLKNI NSINFDNPVY QKTTEDEVHI
CHNQDGYSYP SRQMVSLEDD VA*
Position of stopcodon in wt / mu CDS 2049 / 2049
Position (AA) of stopcodon in wt / mu AA sequence 683 / 683
Position of stopcodon in wt / mu cDNA 2135 / 2135
Position of start ATG in wt / mu cDNA 87 / 87
Last intron/exon boundary 2099
Theoretical NMD boundary in CDS 1962
Length of CDS 2049
Coding sequence (CDS) position 926
cDNA position 1012
gDNA position 23981
Chromosomal position 11113398
Speed 0.34 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:

19:11113398T>C_2_ENST00000455727

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: simple_aae
  • Tree vote: 96|4 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr19:11113398T>C (GRCh38)
Gene symbol LDLR
Gene constraints LOEUF: 1.10, LOF (oe): 0.91, misssense (oe): 0.95, synonymous (oe): 0.97 ? (gnomAD)
Ensembl transcript ID ENST00000455727.6
Genbank transcript ID NM_001195800 (by similarity)
UniProt / AlphaMissense peptide LDLR_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.803T>C
g.23981T>C
AA changes
AAE:V268A?
Score:64
Frameshift No
Length of protein Normal
Pathogenic variant (ClinVar)
Hypercholesterolemia, familial, 1
Cardiovascular phenotype
Familial hypercholesterolemia
pathogenicClinVar OMIM
Variant DBs
dbSNP IDrs779732323
gnomADhomozygous (C/C)heterozygousallele carriers
01313
Protein conservation
SpeciesMatchGeneAAAlignment
Human      268NLRNVVALDTEVASNRIYWSDLSQ
mutated  not conserved    268NLRNVVALDTEAASNRIYWSDLS
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 
22788TOPO_DOMExtracellularlost
22860CHAINlost
234272DOMAINLDL-receptor class Alost
268270STRANDlost
Phylogenetic conservation
PhyloPPhastCons
(flanking)2.0890.98
6.0611
(flanking)-0.0540.859
?
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 19
Strand 1
Original gDNA sequence snippet GGTCGCTCTGGACACGGAGGTGGCCAGCAATAGAATCTACT
Altered gDNA sequence snippet GGTCGCTCTGGACACGGAGGCGGCCAGCAATAGAATCTACT
Original cDNA sequence snippet GGTCGCTCTGGACACGGAGGTGGCCAGCAATAGAATCTACT
Altered cDNA sequence snippet GGTCGCTCTGGACACGGAGGCGGCCAGCAATAGAATCTACT
Wildtype AA sequence MGPWGWKLRW TVALLLAAAG TAVGDRCERN EFQCQDGKCI SYKWVCDGSA ECQDGSDESQ
ETCLSVTCKS GDFSCGGRVN RCIPQFWRCD GQVDCDNGSD EQGCLTLCEG PNKFKCHSGE
CITLDKVCNM ARDCRDWSDE PIKECGTNEC LDNNGGCSHV CNDLKIGYEC LCPDGFQLVA
QRRCEDIDEC QDPDTCSQLC VNLEGGYKCQ CEEGFQLDPH TKACKAVGSI AYLFFTNRHE
VRKMTLDRSE YTSLIPNLRN VVALDTEVAS NRIYWSDLSQ RMICSTQLDR AHGVSSYDTV
ISRDIQAPDG LAVDWIHSNI YWTDSVLGTV SVADTKGVKR KTLFRENGSK PRAIVVDPVH
GFMYWTDWGT PAKIKKGGLN GVDIYSLVTE NIQWPNGITL DLLSGRLYWV DSKLHSISSI
DVNGGNRKTI LEDEKRLAHP FSLAVFEDKV FWTDIINEAI FSANRLTGSD VNLLAENLLS
PEDMVLFHNL TQPRGVNWCE RTTLSNGGCQ YLCLPAPQIN PHSPKFTCAC PDGMLLARDM
RSCLTEAEAA VATQETSTVR LKVSSTAVRT QHTTTRPVPD TSRLPGATPG LTTVEIVTMS
HQALGDVAGR GNEKKPSSVR ALSIVLPIVL LVFLCLGVFL LWKNWRLKNI NSINFDNPVY
QKTTEDEVHI CHNQDGYSYP SRQMVSLEDD VA*
Mutated AA sequence MGPWGWKLRW TVALLLAAAG TAVGDRCERN EFQCQDGKCI SYKWVCDGSA ECQDGSDESQ
ETCLSVTCKS GDFSCGGRVN RCIPQFWRCD GQVDCDNGSD EQGCLTLCEG PNKFKCHSGE
CITLDKVCNM ARDCRDWSDE PIKECGTNEC LDNNGGCSHV CNDLKIGYEC LCPDGFQLVA
QRRCEDIDEC QDPDTCSQLC VNLEGGYKCQ CEEGFQLDPH TKACKAVGSI AYLFFTNRHE
VRKMTLDRSE YTSLIPNLRN VVALDTEAAS NRIYWSDLSQ RMICSTQLDR AHGVSSYDTV
ISRDIQAPDG LAVDWIHSNI YWTDSVLGTV SVADTKGVKR KTLFRENGSK PRAIVVDPVH
GFMYWTDWGT PAKIKKGGLN GVDIYSLVTE NIQWPNGITL DLLSGRLYWV DSKLHSISSI
DVNGGNRKTI LEDEKRLAHP FSLAVFEDKV FWTDIINEAI FSANRLTGSD VNLLAENLLS
PEDMVLFHNL TQPRGVNWCE RTTLSNGGCQ YLCLPAPQIN PHSPKFTCAC PDGMLLARDM
RSCLTEAEAA VATQETSTVR LKVSSTAVRT QHTTTRPVPD TSRLPGATPG LTTVEIVTMS
HQALGDVAGR GNEKKPSSVR ALSIVLPIVL LVFLCLGVFL LWKNWRLKNI NSINFDNPVY
QKTTEDEVHI CHNQDGYSYP SRQMVSLEDD VA*
Position of stopcodon in wt / mu CDS 2079 / 2079
Position (AA) of stopcodon in wt / mu AA sequence 693 / 693
Position of stopcodon in wt / mu cDNA 2165 / 2165
Position of start ATG in wt / mu cDNA 87 / 87
Last intron/exon boundary 2129
Theoretical NMD boundary in CDS 1992
Length of CDS 2079
Coding sequence (CDS) position 803
cDNA position 889
gDNA position 23981
Chromosomal position 11113398
Speed 0.34 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:

19:11113398T>C_7_ENST00000558013

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: simple_aae
  • Tree vote: 96|4 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr19:11113398T>C (GRCh38)
Gene symbol LDLR
Gene constraints LOEUF: 1.12, LOF (oe): 0.94, misssense (oe): 0.95, synonymous (oe): 0.99 ? (gnomAD)
Ensembl transcript ID ENST00000558013.5
Genbank transcript ID NM_001195798 (by similarity)
UniProt / AlphaMissense peptide LDLR_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.1307T>C
g.23981T>C
AA changes
AAE:V436A?
Score:64
Frameshift No
Length of protein Normal
Pathogenic variant (ClinVar)
Hypercholesterolemia, familial, 1
Cardiovascular phenotype
Familial hypercholesterolemia
pathogenicClinVar OMIM
Variant DBs
dbSNP IDrs779732323
gnomADhomozygous (C/C)heterozygousallele carriers
01313
Protein conservation
SpeciesMatchGeneAAAlignment
Human      436NLRNVVALDTEVASNRIYWSDLSQ
mutated  not conserved    436NLRNVVALDTEAASNRIYWSDLS
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 
22788TOPO_DOMExtracellularlost
22860CHAINlost
397438REPEATLDL-receptor class Blost
436439TURNlost
Phylogenetic conservation
PhyloPPhastCons
(flanking)2.0890.98
6.0611
(flanking)-0.0540.859
?
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 19
Strand 1
Original gDNA sequence snippet GGTCGCTCTGGACACGGAGGTGGCCAGCAATAGAATCTACT
Altered gDNA sequence snippet GGTCGCTCTGGACACGGAGGCGGCCAGCAATAGAATCTACT
Original cDNA sequence snippet GGTCGCTCTGGACACGGAGGTGGCCAGCAATAGAATCTACT
Altered cDNA sequence snippet GGTCGCTCTGGACACGGAGGCGGCCAGCAATAGAATCTACT
Wildtype AA sequence MGPWGWKLRW TVALLLAAAG TAVGDRCERN EFQCQDGKCI SYKWVCDGSA ECQDGSDESQ
ETCLSVTCKS GDFSCGGRVN RCIPQFWRCD GQVDCDNGSD EQGCPPKTCS QDEFRCHDGK
CISRQFVCDS DRDCLDGSDE ASCPVLTCGP ASFQCNSSTC IPQLWACDND PDCEDGSDEW
PQRCRGLYVF QGDSSPCSAF EFHCLSGECI HSSWRCDGGP DCKDKSDEEN CAVATCRPDE
FQCSDGNCIH GSRQCDREYD CKDMSDEVGC VNVTLCEGPN KFKCHSGECI TLDKVCNMAR
DCRDWSDEPI KECGTNECLD NNGGCSHVCN DLKIGYECLC PDGFQLVAQR RCEDIDECQD
PDTCSQLCVN LEGGYKCQCE EGFQLDPHTK ACKAVGSIAY LFFTNRHEVR KMTLDRSEYT
SLIPNLRNVV ALDTEVASNR IYWSDLSQRM ICSTQLDRAH GVSSYDTVIS RDIQAPDGLA
VDWIHSNIYW TDSVLGTVSV ADTKGVKRKT LFRENGSKPR AIVVDPVHGF MYWTDWGTPA
KIKKGGLNGV DIYSLVTENI QWPNGITLDL LSGRLYWVDS KLHSISSIDV NGGNRKTILE
DEKRLAHPFS LAVFEDKVFW TDIINEAIFS ANRLTGSDVN LLAENLLSPE DMVLFHNLTQ
PRGVNWCERT TLSNGGCQYL CLPAPQINPH SPKFTCACPD GMLLARDMRS CLTEAEAAVA
TQETSTVRLK VSSTAVRTQH TTTRPVPDTS RLPGATPGLT TVEIVTMSHQ ALGDVAGRGN
EKKPSSVRAL SIVLPIVLLV FLCLGVFLLW KNWRLKNINS INFDNPVYQK TTEDEVHICH
NQDGYSYPSM VSLEDDVA*
Mutated AA sequence MGPWGWKLRW TVALLLAAAG TAVGDRCERN EFQCQDGKCI SYKWVCDGSA ECQDGSDESQ
ETCLSVTCKS GDFSCGGRVN RCIPQFWRCD GQVDCDNGSD EQGCPPKTCS QDEFRCHDGK
CISRQFVCDS DRDCLDGSDE ASCPVLTCGP ASFQCNSSTC IPQLWACDND PDCEDGSDEW
PQRCRGLYVF QGDSSPCSAF EFHCLSGECI HSSWRCDGGP DCKDKSDEEN CAVATCRPDE
FQCSDGNCIH GSRQCDREYD CKDMSDEVGC VNVTLCEGPN KFKCHSGECI TLDKVCNMAR
DCRDWSDEPI KECGTNECLD NNGGCSHVCN DLKIGYECLC PDGFQLVAQR RCEDIDECQD
PDTCSQLCVN LEGGYKCQCE EGFQLDPHTK ACKAVGSIAY LFFTNRHEVR KMTLDRSEYT
SLIPNLRNVV ALDTEAASNR IYWSDLSQRM ICSTQLDRAH GVSSYDTVIS RDIQAPDGLA
VDWIHSNIYW TDSVLGTVSV ADTKGVKRKT LFRENGSKPR AIVVDPVHGF MYWTDWGTPA
KIKKGGLNGV DIYSLVTENI QWPNGITLDL LSGRLYWVDS KLHSISSIDV NGGNRKTILE
DEKRLAHPFS LAVFEDKVFW TDIINEAIFS ANRLTGSDVN LLAENLLSPE DMVLFHNLTQ
PRGVNWCERT TLSNGGCQYL CLPAPQINPH SPKFTCACPD GMLLARDMRS CLTEAEAAVA
TQETSTVRLK VSSTAVRTQH TTTRPVPDTS RLPGATPGLT TVEIVTMSHQ ALGDVAGRGN
EKKPSSVRAL SIVLPIVLLV FLCLGVFLLW KNWRLKNINS INFDNPVYQK TTEDEVHICH
NQDGYSYPSM VSLEDDVA*
Position of stopcodon in wt / mu CDS 2577 / 2577
Position (AA) of stopcodon in wt / mu AA sequence 859 / 859
Position of stopcodon in wt / mu cDNA 2648 / 2648
Position of start ATG in wt / mu cDNA 72 / 72
Last intron/exon boundary 2618
Theoretical NMD boundary in CDS 2496
Length of CDS 2577
Coding sequence (CDS) position 1307
cDNA position 1378
gDNA position 23981
Chromosomal position 11113398
Speed 0.19 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:

19:11113398T>C_1_ENST00000557933

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Prediction:

DeleteriousPermalink

Summary:

  • Model: simple_aae
  • Tree vote: 99|1 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr19:11113398T>C (GRCh38)
Gene symbol LDLR
Gene constraints LOEUF: 1.11, LOF (oe): 0.94, misssense (oe): 0.94, synonymous (oe): 1.00 ? (gnomAD)
Ensembl transcript ID ENST00000557933.5
Genbank transcript ID
UniProt / AlphaMissense peptide N/A
Variant type Single base exchange
Gene region CDS
DNA changes c.1307T>C
g.23981T>C
AA changes
AAE:V436A?
Score:64
Frameshift No
Length of protein Normal
Pathogenic variant (ClinVar)
Hypercholesterolemia, familial, 1
Cardiovascular phenotype
Familial hypercholesterolemia
pathogenicClinVar OMIM
Variant DBs
dbSNP IDrs779732323
gnomADhomozygous (C/C)heterozygousallele carriers
01313
Protein conservation
SpeciesMatchGeneAAAlignment
Human      436NLRNVVALDTEVASNRIYWSDLSQ
mutated  not conserved    436NLRNVVALDTEAASNRIYWSDLS
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)2.0890.98
6.0611
(flanking)-0.0540.859
?
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 19
Strand 1
Original gDNA sequence snippet GGTCGCTCTGGACACGGAGGTGGCCAGCAATAGAATCTACT
Altered gDNA sequence snippet GGTCGCTCTGGACACGGAGGCGGCCAGCAATAGAATCTACT
Original cDNA sequence snippet GGTCGCTCTGGACACGGAGGTGGCCAGCAATAGAATCTACT
Altered cDNA sequence snippet GGTCGCTCTGGACACGGAGGCGGCCAGCAATAGAATCTACT
Wildtype AA sequence MGPWGWKLRW TVALLLAAAG TAVGDRCERN EFQCQDGKCI SYKWVCDGSA ECQDGSDESQ
ETCLSVTCKS GDFSCGGRVN RCIPQFWRCD GQVDCDNGSD EQGCPPKTCS QDEFRCHDGK
CISRQFVCDS DRDCLDGSDE ASCPVLTCGP ASFQCNSSTC IPQLWACDND PDCEDGSDEW
PQRCRGLYVF QGDSSPCSAF EFHCLSGECI HSSWRCDGGP DCKDKSDEEN CAVATCRPDE
FQCSDGNCIH GSRQCDREYD CKDMSDEVGC VNVTLCEGPN KFKCHSGECI TLDKVCNMAR
DCRDWSDEPI KECGTNECLD NNGGCSHVCN DLKIGYECLC PDGFQLVAQR RCEDIDECQD
PDTCSQLCVN LEGGYKCQCE EGFQLDPHTK ACKAVGSIAY LFFTNRHEVR KMTLDRSEYT
SLIPNLRNVV ALDTEVASNR IYWSDLSQRM ICSTQLDRAH GVSSYDTVIS RDIQAPDGLA
VDWIHSNIYW TDSVLGTVSV ADTKGVKRKT LFRENGSKPR AIVVDPVHGF MYWTDWGTPA
KIKKGGLNGV DIYSLVTENI QWPNGITLDL LSGRLYWVDS KLHSISSIDV NGGNRKTILE
DEKRLAHPFS LAVFEDKVFW TDIINEAIFS ANRLTGSDVN LLAENLLSPE DMVLFHNLTQ
PRGVNWCERT TLSNGGCQYL CLPAPQINPH SPKFTCACPD GMLLARDMRS CLTEAEAAVA
TQETSTVRLK VSSTAVRTQH TTTRPVPDTS RLPGATPGLT TVEIVTMSHQ ALGDVAGRGN
EKKPSSVRAL SIVLPIATEL GLWSRGQLCD RACLSLQCSS SSFAWGSSFY GRTGGLRTST
ASTLTTPSIR RPQRMRSTFA TTRTATATPR DRWSVWRMTW REHLPGVPSL PRTLPETSPA
LFYSKTEKTK ALPARALFYI FIHLGGRTGF GQCPCNGLGW DFGFFLSS*
Mutated AA sequence MGPWGWKLRW TVALLLAAAG TAVGDRCERN EFQCQDGKCI SYKWVCDGSA ECQDGSDESQ
ETCLSVTCKS GDFSCGGRVN RCIPQFWRCD GQVDCDNGSD EQGCPPKTCS QDEFRCHDGK
CISRQFVCDS DRDCLDGSDE ASCPVLTCGP ASFQCNSSTC IPQLWACDND PDCEDGSDEW
PQRCRGLYVF QGDSSPCSAF EFHCLSGECI HSSWRCDGGP DCKDKSDEEN CAVATCRPDE
FQCSDGNCIH GSRQCDREYD CKDMSDEVGC VNVTLCEGPN KFKCHSGECI TLDKVCNMAR
DCRDWSDEPI KECGTNECLD NNGGCSHVCN DLKIGYECLC PDGFQLVAQR RCEDIDECQD
PDTCSQLCVN LEGGYKCQCE EGFQLDPHTK ACKAVGSIAY LFFTNRHEVR KMTLDRSEYT
SLIPNLRNVV ALDTEAASNR IYWSDLSQRM ICSTQLDRAH GVSSYDTVIS RDIQAPDGLA
VDWIHSNIYW TDSVLGTVSV ADTKGVKRKT LFRENGSKPR AIVVDPVHGF MYWTDWGTPA
KIKKGGLNGV DIYSLVTENI QWPNGITLDL LSGRLYWVDS KLHSISSIDV NGGNRKTILE
DEKRLAHPFS LAVFEDKVFW TDIINEAIFS ANRLTGSDVN LLAENLLSPE DMVLFHNLTQ
PRGVNWCERT TLSNGGCQYL CLPAPQINPH SPKFTCACPD GMLLARDMRS CLTEAEAAVA
TQETSTVRLK VSSTAVRTQH TTTRPVPDTS RLPGATPGLT TVEIVTMSHQ ALGDVAGRGN
EKKPSSVRAL SIVLPIATEL GLWSRGQLCD RACLSLQCSS SSFAWGSSFY GRTGGLRTST
ASTLTTPSIR RPQRMRSTFA TTRTATATPR DRWSVWRMTW REHLPGVPSL PRTLPETSPA
LFYSKTEKTK ALPARALFYI FIHLGGRTGF GQCPCNGLGW DFGFFLSS*
Position of stopcodon in wt / mu CDS 2847 / 2847
Position (AA) of stopcodon in wt / mu AA sequence 949 / 949
Position of stopcodon in wt / mu cDNA 2934 / 2934
Position of start ATG in wt / mu cDNA 88 / 88
Last intron/exon boundary 2696
Theoretical NMD boundary in CDS 2558
Length of CDS 2847
Coding sequence (CDS) position 1307
cDNA position 1394
gDNA position 23981
Chromosomal position 11113398
Speed 0.39 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:

19:11113398T>C_6_ENST00000560467

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Prediction:

DeleteriousPermalink

Summary:

  • Model: simple_aae
  • Tree vote: 99|1 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr19:11113398T>C (GRCh38)
Gene symbol LDLR
Gene constraints LOEUF: 1.26, LOF (oe): 0.94, misssense (oe): 1.02, synonymous (oe): 1.00 ? (gnomAD)
Ensembl transcript ID ENST00000560467.2
Genbank transcript ID
UniProt / AlphaMissense peptide N/A
Variant type Single base exchange
Gene region CDS
DNA changes c.1187T>C
g.23981T>C
AA changes
AAE:V396A?
Score:64
Frameshift No
Length of protein Normal
Pathogenic variant (ClinVar)
Hypercholesterolemia, familial, 1
Cardiovascular phenotype
Familial hypercholesterolemia
pathogenicClinVar OMIM
Variant DBs
dbSNP IDrs779732323
gnomADhomozygous (C/C)heterozygousallele carriers
01313
Protein conservation
SpeciesMatchGeneAAAlignment
Human      396NLRNVVALDTEVASNRIYWSDLSQ
mutated  not conserved    396NLRNVVALDTEAASNRIYWSDLS
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)2.0890.98
6.0611
(flanking)-0.0540.859
?
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 19
Strand 1
Original gDNA sequence snippet GGTCGCTCTGGACACGGAGGTGGCCAGCAATAGAATCTACT
Altered gDNA sequence snippet GGTCGCTCTGGACACGGAGGCGGCCAGCAATAGAATCTACT
Original cDNA sequence snippet GGTCGCTCTGGACACGGAGGTGGCCAGCAATAGAATCTACT
Altered cDNA sequence snippet GGTCGCTCTGGACACGGAGGCGGCCAGCAATAGAATCTACT
Wildtype AA sequence MGPWGWKLRW TVALLLAAAG TAVGDRCERN EFQCQDGKCI SYKWVCDGSA ECQDGSDESQ
ETCLSVTCKS GDFSCGGRVN RCIPQFWRCD GQVDCDNGSD EQGCPPKTCS QDEFRCHDGK
CISRQFVCDS DRDCLDGSDE ASCPVLTCGP ASFQCNSSTC IPQLWACDND PDCEDGSDEW
PQRCRGLYVF QGDSSPCSAF EFHCLSGECI HSSWRCDGGP DCKDKSDEEN CAVATCRPDE
FQCSDGNCIH GSRQCDREYD CKDMSDEVGC VNVTLCEGPN KFKCHSGECI TLDKVCNMAR
DCRDWSDEPI KECDIDECQD PDTCSQLCVN LEGGYKCQCE EGFQLDPHTK ACKAVGSIAY
LFFTNRHEVR KMTLDRSEYT SLIPNLRNVV ALDTEVASNR IYWSDLSQRM ICSTQLDRAH
GVSSYDTVIS RDIQAPDGLA VDWIHSNIYW TDSVLGTVSV ADTKGVKRKT LFRENGSKPR
AIVVDPVHGF MYWTDWGTPA KIKKGGLNGV DIYSLVTENI QWPNGITLDL LSGRLYWVDS
KLHSISSIDV NGGNRKTILE DEKRLAHPFS LAVFEDKVFW TDIINEAIFS ANRLTGSDVN
LLAENLLSPE DMVLFHNLTQ PRGVNWCERT TLSNGGCQYL CLPAPQINPH SPKFTCACPD
GMLLARDMRS CLTEAEAAVA TQETSTVRLK VSSTAVRTQH TTTRPVPDTS RLPGATPGLT
TVEIVTMSHQ ALGDVAGRGN EKKPSSVRAL SIVLPIVLLV FLCLGVFLLW KNWRLKNINS
INFDNPVYQK TTEDEVHICH NQDGYSYPSR QMVSLEDDVA *
Mutated AA sequence MGPWGWKLRW TVALLLAAAG TAVGDRCERN EFQCQDGKCI SYKWVCDGSA ECQDGSDESQ
ETCLSVTCKS GDFSCGGRVN RCIPQFWRCD GQVDCDNGSD EQGCPPKTCS QDEFRCHDGK
CISRQFVCDS DRDCLDGSDE ASCPVLTCGP ASFQCNSSTC IPQLWACDND PDCEDGSDEW
PQRCRGLYVF QGDSSPCSAF EFHCLSGECI HSSWRCDGGP DCKDKSDEEN CAVATCRPDE
FQCSDGNCIH GSRQCDREYD CKDMSDEVGC VNVTLCEGPN KFKCHSGECI TLDKVCNMAR
DCRDWSDEPI KECDIDECQD PDTCSQLCVN LEGGYKCQCE EGFQLDPHTK ACKAVGSIAY
LFFTNRHEVR KMTLDRSEYT SLIPNLRNVV ALDTEAASNR IYWSDLSQRM ICSTQLDRAH
GVSSYDTVIS RDIQAPDGLA VDWIHSNIYW TDSVLGTVSV ADTKGVKRKT LFRENGSKPR
AIVVDPVHGF MYWTDWGTPA KIKKGGLNGV DIYSLVTENI QWPNGITLDL LSGRLYWVDS
KLHSISSIDV NGGNRKTILE DEKRLAHPFS LAVFEDKVFW TDIINEAIFS ANRLTGSDVN
LLAENLLSPE DMVLFHNLTQ PRGVNWCERT TLSNGGCQYL CLPAPQINPH SPKFTCACPD
GMLLARDMRS CLTEAEAAVA TQETSTVRLK VSSTAVRTQH TTTRPVPDTS RLPGATPGLT
TVEIVTMSHQ ALGDVAGRGN EKKPSSVRAL SIVLPIVLLV FLCLGVFLLW KNWRLKNINS
INFDNPVYQK TTEDEVHICH NQDGYSYPSR QMVSLEDDVA *
Position of stopcodon in wt / mu CDS 2463 / 2463
Position (AA) of stopcodon in wt / mu AA sequence 821 / 821
Position of stopcodon in wt / mu cDNA 2548 / 2548
Position of start ATG in wt / mu cDNA 86 / 86
Last intron/exon boundary 2512
Theoretical NMD boundary in CDS 2376
Length of CDS 2463
Coding sequence (CDS) position 1187
cDNA position 1272
gDNA position 23981
Chromosomal position 11113398
Speed 0.37 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:

19:11113398T>C_5_ENST00000558518

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: simple_aae
  • Tree vote: 99|1 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr19:11113398T>C (GRCh38)
Gene symbol LDLR
Gene constraints LOEUF: 1.09, LOF (oe): 0.92, misssense (oe): 0.95, synonymous (oe): 0.99 ? (gnomAD)
Ensembl transcript ID ENST00000558518.6
Genbank transcript ID NM_000527 (exact from MANE)
UniProt / AlphaMissense peptide LDLR_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.1307T>C
g.23981T>C
AA changes
AAE:V436A?
Score:64
Frameshift No
Length of protein Normal
Pathogenic variant (ClinVar)
Hypercholesterolemia, familial, 1
Cardiovascular phenotype
Familial hypercholesterolemia
pathogenicClinVar OMIM
Variant DBs
dbSNP IDrs779732323
gnomADhomozygous (C/C)heterozygousallele carriers
01313
Protein conservation
SpeciesMatchGeneAAAlignment
Human      436NLRNVVALDTEVASNRIYWSDLSQ
mutated  not conserved    436NLRNVVALDTEAASNRIYWSDLS
Ptroglodytes  all identical    436NLRNVVALDTEVASNRIYWSDLS
Mmulatta  all identical    436NLRNVVALDTEVASNRIYWSDLS
Fcatus  all identical    438NLKNVVALDTEVASNRIYWSDLS
Mmusculus  all identical    437NVVALDTEVTNNRIYWSDLS
Ggallus  no homologue    
Trubripes  no homologue    
Drerio  no homologue    
Dmelanogaster  not conserved    1082VAQMAIGLDKDCVEGRVYWGDIS
Celegans  no homologue    
Xtropicalis  all conserved    426RLKNVVALDMEIASNKIYWSD
Protein features
Start (aa)End (aa)FeatureDetails 
22788TOPO_DOMExtracellularlost
22860CHAINlost
397438REPEATLDL-receptor class Blost
436439TURNlost
Phylogenetic conservation
PhyloPPhastCons
(flanking)2.0890.98
6.0611
(flanking)-0.0540.859
?
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 19
Strand 1
Original gDNA sequence snippet GGTCGCTCTGGACACGGAGGTGGCCAGCAATAGAATCTACT
Altered gDNA sequence snippet GGTCGCTCTGGACACGGAGGCGGCCAGCAATAGAATCTACT
Original cDNA sequence snippet GGTCGCTCTGGACACGGAGGTGGCCAGCAATAGAATCTACT
Altered cDNA sequence snippet GGTCGCTCTGGACACGGAGGCGGCCAGCAATAGAATCTACT
Wildtype AA sequence MGPWGWKLRW TVALLLAAAG TAVGDRCERN EFQCQDGKCI SYKWVCDGSA ECQDGSDESQ
ETCLSVTCKS GDFSCGGRVN RCIPQFWRCD GQVDCDNGSD EQGCPPKTCS QDEFRCHDGK
CISRQFVCDS DRDCLDGSDE ASCPVLTCGP ASFQCNSSTC IPQLWACDND PDCEDGSDEW
PQRCRGLYVF QGDSSPCSAF EFHCLSGECI HSSWRCDGGP DCKDKSDEEN CAVATCRPDE
FQCSDGNCIH GSRQCDREYD CKDMSDEVGC VNVTLCEGPN KFKCHSGECI TLDKVCNMAR
DCRDWSDEPI KECGTNECLD NNGGCSHVCN DLKIGYECLC PDGFQLVAQR RCEDIDECQD
PDTCSQLCVN LEGGYKCQCE EGFQLDPHTK ACKAVGSIAY LFFTNRHEVR KMTLDRSEYT
SLIPNLRNVV ALDTEVASNR IYWSDLSQRM ICSTQLDRAH GVSSYDTVIS RDIQAPDGLA
VDWIHSNIYW TDSVLGTVSV ADTKGVKRKT LFRENGSKPR AIVVDPVHGF MYWTDWGTPA
KIKKGGLNGV DIYSLVTENI QWPNGITLDL LSGRLYWVDS KLHSISSIDV NGGNRKTILE
DEKRLAHPFS LAVFEDKVFW TDIINEAIFS ANRLTGSDVN LLAENLLSPE DMVLFHNLTQ
PRGVNWCERT TLSNGGCQYL CLPAPQINPH SPKFTCACPD GMLLARDMRS CLTEAEAAVA
TQETSTVRLK VSSTAVRTQH TTTRPVPDTS RLPGATPGLT TVEIVTMSHQ ALGDVAGRGN
EKKPSSVRAL SIVLPIVLLV FLCLGVFLLW KNWRLKNINS INFDNPVYQK TTEDEVHICH
NQDGYSYPSR QMVSLEDDVA *
Mutated AA sequence MGPWGWKLRW TVALLLAAAG TAVGDRCERN EFQCQDGKCI SYKWVCDGSA ECQDGSDESQ
ETCLSVTCKS GDFSCGGRVN RCIPQFWRCD GQVDCDNGSD EQGCPPKTCS QDEFRCHDGK
CISRQFVCDS DRDCLDGSDE ASCPVLTCGP ASFQCNSSTC IPQLWACDND PDCEDGSDEW
PQRCRGLYVF QGDSSPCSAF EFHCLSGECI HSSWRCDGGP DCKDKSDEEN CAVATCRPDE
FQCSDGNCIH GSRQCDREYD CKDMSDEVGC VNVTLCEGPN KFKCHSGECI TLDKVCNMAR
DCRDWSDEPI KECGTNECLD NNGGCSHVCN DLKIGYECLC PDGFQLVAQR RCEDIDECQD
PDTCSQLCVN LEGGYKCQCE EGFQLDPHTK ACKAVGSIAY LFFTNRHEVR KMTLDRSEYT
SLIPNLRNVV ALDTEAASNR IYWSDLSQRM ICSTQLDRAH GVSSYDTVIS RDIQAPDGLA
VDWIHSNIYW TDSVLGTVSV ADTKGVKRKT LFRENGSKPR AIVVDPVHGF MYWTDWGTPA
KIKKGGLNGV DIYSLVTENI QWPNGITLDL LSGRLYWVDS KLHSISSIDV NGGNRKTILE
DEKRLAHPFS LAVFEDKVFW TDIINEAIFS ANRLTGSDVN LLAENLLSPE DMVLFHNLTQ
PRGVNWCERT TLSNGGCQYL CLPAPQINPH SPKFTCACPD GMLLARDMRS CLTEAEAAVA
TQETSTVRLK VSSTAVRTQH TTTRPVPDTS RLPGATPGLT TVEIVTMSHQ ALGDVAGRGN
EKKPSSVRAL SIVLPIVLLV FLCLGVFLLW KNWRLKNINS INFDNPVYQK TTEDEVHICH
NQDGYSYPSR QMVSLEDDVA *
Position of stopcodon in wt / mu CDS 2583 / 2583
Position (AA) of stopcodon in wt / mu AA sequence 861 / 861
Position of stopcodon in wt / mu cDNA 2669 / 2669
Position of start ATG in wt / mu cDNA 87 / 87
Last intron/exon boundary 2633
Theoretical NMD boundary in CDS 2496
Length of CDS 2583
Coding sequence (CDS) position 1307
cDNA position 1393
gDNA position 23981
Chromosomal position 11113398
Speed 0.36 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:

19:11113398T>C_8_ENST00000252444

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: simple_aae
  • Tree vote: 99|1 (del | benign) ?
  • Automatic classification due to ClinVar
Analysed issue Analysis result
Variant Chr19:11113398T>C (GRCh38)
Gene symbol LDLR
Gene constraints LOEUF: 1.09, LOF (oe): 0.92, misssense (oe): 0.95, synonymous (oe): 1.00 ? (gnomAD)
Ensembl transcript ID ENST00000252444.10
Genbank transcript ID
UniProt / AlphaMissense peptide N/A
Variant type Single base exchange
Gene region CDS
DNA changes c.1565T>C
g.23981T>C
AA changes
AAE:V522A?
Score:64
Frameshift No
Length of protein Normal
Pathogenic variant (ClinVar)
Hypercholesterolemia, familial, 1
Cardiovascular phenotype
Familial hypercholesterolemia
pathogenicClinVar OMIM
Variant DBs
dbSNP IDrs779732323
gnomADhomozygous (C/C)heterozygousallele carriers
01313
Protein conservation
SpeciesMatchGeneAAAlignment
Human      522NLRNVVALDTEVASNRIYWSDLSQ
mutated  not conserved    522NLRNVVALDTEAASNRIYWSDLS
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)2.0890.98
6.0611
(flanking)-0.0540.859
?
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 19
Strand 1
Original gDNA sequence snippet GGTCGCTCTGGACACGGAGGTGGCCAGCAATAGAATCTACT
Altered gDNA sequence snippet GGTCGCTCTGGACACGGAGGCGGCCAGCAATAGAATCTACT
Original cDNA sequence snippet GGTCGCTCTGGACACGGAGGTGGCCAGCAATAGAATCTACT
Altered cDNA sequence snippet GGTCGCTCTGGACACGGAGGCGGCCAGCAATAGAATCTACT
Wildtype AA sequence MQGRPGVPPR FLSQRRRQVP GPRSRLRDIH ESPSVILGPP GEVPGFRCAL WRHLRPHLVL
GGALAPPAPI KFTEGPPATL KASVPYEVET LPQNLPAPPW SAAEIFSHVG DRCERNEFQC
QDGKCISYKW VCDGSAECQD GSDESQETCL SVTCKSGDFS CGGRVNRCIP QFWRCDGQVD
CDNGSDEQGC PPKTCSQDEF RCHDGKCISR QFVCDSDRDC LDGSDEASCP VLTCGPASFQ
CNSSTCIPQL WACDNDPDCE DGSDEWPQRC RGLYVFQGDS SPCSAFEFHC LSGECIHSSW
RCDGGPDCKD KSDEENCAVA TCRPDEFQCS DGNCIHGSRQ CDREYDCKDM SDEVGCVNVT
LCEGPNKFKC HSGECITLDK VCNMARDCRD WSDEPIKECG TNECLDNNGG CSHVCNDLKI
GYECLCPDGF QLVAQRRCED IDECQDPDTC SQLCVNLEGG YKCQCEEGFQ LDPHTKACKA
VGSIAYLFFT NRHEVRKMTL DRSEYTSLIP NLRNVVALDT EVASNRIYWS DLSQRMICST
QLDRAHGVSS YDTVISRDIQ APDGLAVDWI HSNIYWTDSV LGTVSVADTK GVKRKTLFRE
NGSKPRAIVV DPVHGFMYWT DWGTPAKIKK GGLNGVDIYS LVTENIQWPN GITLDLLSGR
LYWVDSKLHS ISSIDVNGGN RKTILEDEKR LAHPFSLAVF EDKVFWTDII NEAIFSANRL
TGSDVNLLAE NLLSPEDMVL FHNLTQPRGV NWCERTTLSN GGCQYLCLPA PQINPHSPKF
TCACPDGMLL ARDMRSCLTE AEAAVATQET STVRLKVSST AVRTQHTTTR PVPDTSRLPG
ATPGLTTVEI VTMSHQALGD VAGRGNEKKP SSVRALSIVL PIVLLVFLCL GVFLLWKNWR
LKNINSINFD NPVYQKTTED EVHICHNQDG YSYPSRQMVS LEDDVA*
Mutated AA sequence MQGRPGVPPR FLSQRRRQVP GPRSRLRDIH ESPSVILGPP GEVPGFRCAL WRHLRPHLVL
GGALAPPAPI KFTEGPPATL KASVPYEVET LPQNLPAPPW SAAEIFSHVG DRCERNEFQC
QDGKCISYKW VCDGSAECQD GSDESQETCL SVTCKSGDFS CGGRVNRCIP QFWRCDGQVD
CDNGSDEQGC PPKTCSQDEF RCHDGKCISR QFVCDSDRDC LDGSDEASCP VLTCGPASFQ
CNSSTCIPQL WACDNDPDCE DGSDEWPQRC RGLYVFQGDS SPCSAFEFHC LSGECIHSSW
RCDGGPDCKD KSDEENCAVA TCRPDEFQCS DGNCIHGSRQ CDREYDCKDM SDEVGCVNVT
LCEGPNKFKC HSGECITLDK VCNMARDCRD WSDEPIKECG TNECLDNNGG CSHVCNDLKI
GYECLCPDGF QLVAQRRCED IDECQDPDTC SQLCVNLEGG YKCQCEEGFQ LDPHTKACKA
VGSIAYLFFT NRHEVRKMTL DRSEYTSLIP NLRNVVALDT EAASNRIYWS DLSQRMICST
QLDRAHGVSS YDTVISRDIQ APDGLAVDWI HSNIYWTDSV LGTVSVADTK GVKRKTLFRE
NGSKPRAIVV DPVHGFMYWT DWGTPAKIKK GGLNGVDIYS LVTENIQWPN GITLDLLSGR
LYWVDSKLHS ISSIDVNGGN RKTILEDEKR LAHPFSLAVF EDKVFWTDII NEAIFSANRL
TGSDVNLLAE NLLSPEDMVL FHNLTQPRGV NWCERTTLSN GGCQYLCLPA PQINPHSPKF
TCACPDGMLL ARDMRSCLTE AEAAVATQET STVRLKVSST AVRTQHTTTR PVPDTSRLPG
ATPGLTTVEI VTMSHQALGD VAGRGNEKKP SSVRALSIVL PIVLLVFLCL GVFLLWKNWR
LKNINSINFD NPVYQKTTED EVHICHNQDG YSYPSRQMVS LEDDVA*
Position of stopcodon in wt / mu CDS 2841 / 2841
Position (AA) of stopcodon in wt / mu AA sequence 947 / 947
Position of stopcodon in wt / mu cDNA 2857 / 2857
Position of start ATG in wt / mu cDNA 17 / 17
Last intron/exon boundary 2821
Theoretical NMD boundary in CDS 2754
Length of CDS 2841
Coding sequence (CDS) position 1565
cDNA position 1581
gDNA position 23981
Chromosomal position 11113398
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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