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: ENST00000393087
Querying Taster for transcript #2: ENST00000440909
Querying Taster for transcript #3: ENST00000355814
Querying Taster for transcript #4: ENST00000437397
Querying Taster for transcript #5: ENST00000448921
Querying Taster for transcript #6: ENST00000636712
Querying Taster for transcript #7: ENST00000393088
Querying Taster for transcript #8: ENST00000404814
Querying Taster for transcript #9: ENST00000449399
MT speed 0.95 s - this script 3.475066 s

Transcript summary:

Permalink

Yum, tasty mutations...

MutationT@ster 2025

Variant:

14:94378610C>A_2_ENST00000440909

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
Analysed issue Analysis result
Variant Chr14:94378610C>A (GRCh38)
Gene symbol SERPINA1
Gene constraints LOEUF: 1.13, LOF (oe): 0.79, misssense (oe): 1.02, synonymous (oe): 1.00 ? (gnomAD)
Ensembl transcript ID ENST00000440909.5
Genbank transcript ID NM_001002235 (by similarity), NM_001127700 (by similarity)
UniProt / AlphaMissense peptide A1AT_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.1096G>T
g.12084G>T
AA changes
AAE:E366*K367-G368-T369-E370-A371-A372-G373-A374-M375-F376-L377-E378-A379-I380-P381-M382-S383-I384-P385-P386-E387-V388-K389-F390-N391-K392-P393-F394-V395-F396-L397-M398-I399-E400-Q401-N402-T403-K404-S405-P406-L407-F408-M409-G410-K411-V412-V413-N414-P415-T416-Q417-K418-*419-?
Score:------------------------------------------------------
Frameshift No
Length of protein Strongly truncated protein, might cause NMD (-53 AA / more than 10% missing)
Pathogenic variant (ClinVar) Variant not listed in ClinVar as (likely) pathogenic.
Variant DBs
Not in dbSNP
gnomADhomozygous (A/A)heterozygousallele carriers
011
Protein conservation
SpeciesMatchGeneAAAlignment
Human      366KAVHKAVLTIDEKGTEAAGAMFLE
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 
25418CHAINlost
366381STRANDlost
368392REGIONlost
375418PEPTIDElost
382383SITEReactive bondlost
383383MOD_RESPhosphoserinelost
387389STRANDlost
394400STRANDlost
401403TURNlost
406414STRANDlost
Phylogenetic conservation
PhyloPPhastCons
(flanking)5.3571
5.271
(flanking)-0.3430.234
?
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 14
Strand -1
Original gDNA sequence snippet AGGCTGTGCTGACCATCGACGAGAAAGGGACTGAAGCTGCT
Altered gDNA sequence snippet AGGCTGTGCTGACCATCGACTAGAAAGGGACTGAAGCTGCT
Original cDNA sequence snippet AGGCTGTGCTGACCATCGACGAGAAAGGGACTGAAGCTGCT
Altered cDNA sequence snippet AGGCTGTGCTGACCATCGACTAGAAAGGGACTGAAGCTGCT
Wildtype AA sequence MPSSVSWGIL LLAGLCCLVP VSLAEDPQGD AAQKTDTSHH DQDHPTFNKI TPNLAEFAFS
LYRQLAHQSN STNIFFSPVS IATAFAMLSL GTKADTHDEI LEGLNFNLTE IPEAQIHEGF
QELLRTLNQP DSQLQLTTGN GLFLSEGLKL VDKFLEDVKK LYHSEAFTVN FGDTEEAKKQ
INDYVEKGTQ GKIVDLVKEL DRDTVFALVN YIFFKGKWER PFEVKDTEEE DFHVDQVTTV
KVPMMKRLGM FNIQHCKKLS SWVLLMKYLG NATAIFFLPD EGKLQHLENE LTHDIITKFL
ENEDRRSASL HLPKLSITGT YDLKSVLGQL GITKVFSNGA DLSGVTEEAP LKLSKAVHKA
VLTIDEKGTE AAGAMFLEAI PMSIPPEVKF NKPFVFLMIE QNTKSPLFMG KVVNPTQK*
Mutated AA sequence MPSSVSWGIL LLAGLCCLVP VSLAEDPQGD AAQKTDTSHH DQDHPTFNKI TPNLAEFAFS
LYRQLAHQSN STNIFFSPVS IATAFAMLSL GTKADTHDEI LEGLNFNLTE IPEAQIHEGF
QELLRTLNQP DSQLQLTTGN GLFLSEGLKL VDKFLEDVKK LYHSEAFTVN FGDTEEAKKQ
INDYVEKGTQ GKIVDLVKEL DRDTVFALVN YIFFKGKWER PFEVKDTEEE DFHVDQVTTV
KVPMMKRLGM FNIQHCKKLS SWVLLMKYLG NATAIFFLPD EGKLQHLENE LTHDIITKFL
ENEDRRSASL HLPKLSITGT YDLKSVLGQL GITKVFSNGA DLSGVTEEAP LKLSKAVHKA
VLTID*
Position of stopcodon in wt / mu CDS 1257 / 1098
Position (AA) of stopcodon in wt / mu AA sequence 419 / 366
Position of stopcodon in wt / mu cDNA 1442 / 1283
Position of start ATG in wt / mu cDNA 186 / 186
Last intron/exon boundary 1250
Theoretical NMD boundary in CDS 1014
Length of CDS 1257
Coding sequence (CDS) position 1096
cDNA position 1281
gDNA position 12084
Chromosomal position 94378610
Speed 0.09 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:

14:94378610C>A_3_ENST00000355814

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
Analysed issue Analysis result
Variant Chr14:94378610C>A (GRCh38)
Gene symbol SERPINA1
Gene constraints LOEUF: 1.13, LOF (oe): 0.79, misssense (oe): 1.02, synonymous (oe): 1.00 ? (gnomAD)
Ensembl transcript ID ENST00000355814.8
Genbank transcript ID
UniProt / AlphaMissense peptide A1AT_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.1096G>T
g.12084G>T
AA changes
AAE:E366*K367-G368-T369-E370-A371-A372-G373-A374-M375-F376-L377-E378-A379-I380-P381-M382-S383-I384-P385-P386-E387-V388-K389-F390-N391-K392-P393-F394-V395-F396-L397-M398-I399-E400-Q401-N402-T403-K404-S405-P406-L407-F408-M409-G410-K411-V412-V413-N414-P415-T416-Q417-K418-*419-?
Score:------------------------------------------------------
Frameshift No
Length of protein Strongly truncated protein, might cause NMD (-53 AA / more than 10% missing)
Pathogenic variant (ClinVar) Variant not listed in ClinVar as (likely) pathogenic.
Variant DBs
Not in dbSNP
gnomADhomozygous (A/A)heterozygousallele carriers
011
Protein conservation
SpeciesMatchGeneAAAlignment
Human      366KAVHKAVLTIDEKGTEAAGAMFLE
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 
25418CHAINlost
366381STRANDlost
368392REGIONlost
375418PEPTIDElost
382383SITEReactive bondlost
383383MOD_RESPhosphoserinelost
387389STRANDlost
394400STRANDlost
401403TURNlost
406414STRANDlost
Phylogenetic conservation
PhyloPPhastCons
(flanking)5.3571
5.271
(flanking)-0.3430.234
?
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 14
Strand -1
Original gDNA sequence snippet AGGCTGTGCTGACCATCGACGAGAAAGGGACTGAAGCTGCT
Altered gDNA sequence snippet AGGCTGTGCTGACCATCGACTAGAAAGGGACTGAAGCTGCT
Original cDNA sequence snippet AGGCTGTGCTGACCATCGACGAGAAAGGGACTGAAGCTGCT
Altered cDNA sequence snippet AGGCTGTGCTGACCATCGACTAGAAAGGGACTGAAGCTGCT
Wildtype AA sequence MPSSVSWGIL LLAGLCCLVP VSLAEDPQGD AAQKTDTSHH DQDHPTFNKI TPNLAEFAFS
LYRQLAHQSN STNIFFSPVS IATAFAMLSL GTKADTHDEI LEGLNFNLTE IPEAQIHEGF
QELLRTLNQP DSQLQLTTGN GLFLSEGLKL VDKFLEDVKK LYHSEAFTVN FGDTEEAKKQ
INDYVEKGTQ GKIVDLVKEL DRDTVFALVN YIFFKGKWER PFEVKDTEEE DFHVDQVTTV
KVPMMKRLGM FNIQHCKKLS SWVLLMKYLG NATAIFFLPD EGKLQHLENE LTHDIITKFL
ENEDRRSASL HLPKLSITGT YDLKSVLGQL GITKVFSNGA DLSGVTEEAP LKLSKAVHKA
VLTIDEKGTE AAGAMFLEAI PMSIPPEVKF NKPFVFLMIE QNTKSPLFMG KVVNPTQK*
Mutated AA sequence MPSSVSWGIL LLAGLCCLVP VSLAEDPQGD AAQKTDTSHH DQDHPTFNKI TPNLAEFAFS
LYRQLAHQSN STNIFFSPVS IATAFAMLSL GTKADTHDEI LEGLNFNLTE IPEAQIHEGF
QELLRTLNQP DSQLQLTTGN GLFLSEGLKL VDKFLEDVKK LYHSEAFTVN FGDTEEAKKQ
INDYVEKGTQ GKIVDLVKEL DRDTVFALVN YIFFKGKWER PFEVKDTEEE DFHVDQVTTV
KVPMMKRLGM FNIQHCKKLS SWVLLMKYLG NATAIFFLPD EGKLQHLENE LTHDIITKFL
ENEDRRSASL HLPKLSITGT YDLKSVLGQL GITKVFSNGA DLSGVTEEAP LKLSKAVHKA
VLTID*
Position of stopcodon in wt / mu CDS 1257 / 1098
Position (AA) of stopcodon in wt / mu AA sequence 419 / 366
Position of stopcodon in wt / mu cDNA 1534 / 1375
Position of start ATG in wt / mu cDNA 278 / 278
Last intron/exon boundary 1342
Theoretical NMD boundary in CDS 1014
Length of CDS 1257
Coding sequence (CDS) position 1096
cDNA position 1373
gDNA position 12084
Chromosomal position 94378610
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:

14:94378610C>A_1_ENST00000393087

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
Analysed issue Analysis result
Variant Chr14:94378610C>A (GRCh38)
Gene symbol SERPINA1
Gene constraints LOEUF: 1.13, LOF (oe): 0.79, misssense (oe): 1.02, synonymous (oe): 1.00 ? (gnomAD)
Ensembl transcript ID ENST00000393087.9
Genbank transcript ID NM_000295 (exact from MANE)
UniProt / AlphaMissense peptide A1AT_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.1096G>T
g.12084G>T
AA changes
AAE:E366*K367-G368-T369-E370-A371-A372-G373-A374-M375-F376-L377-E378-A379-I380-P381-M382-S383-I384-P385-P386-E387-V388-K389-F390-N391-K392-P393-F394-V395-F396-L397-M398-I399-E400-Q401-N402-T403-K404-S405-P406-L407-F408-M409-G410-K411-V412-V413-N414-P415-T416-Q417-K418-*419-?
Score:------------------------------------------------------
Frameshift No
Length of protein Strongly truncated protein, might cause NMD (-53 AA / more than 10% missing)
Pathogenic variant (ClinVar) Variant not listed in ClinVar as (likely) pathogenic.
Variant DBs
Not in dbSNP
gnomADhomozygous (A/A)heterozygousallele carriers
011
Protein conservation
SpeciesMatchGeneAAAlignment
Human      366KAVHKAVLTIDEKGTEAAGAMFLEAIPMSIPPEVKFNKPFVFLMIEQNTKSPLFMGKVVNPTQK*
mutated  no alignment    n/a
Ptroglodytes  all conserved    366VLTIDEKGTEAAGAMFLEAIPMSIPPEVKFNKPFVFLMIEQNTKSPLFVGKVVNPTQK
Mmulatta  all conserved    406VLTIDEKGTEAAGAMFLEAIPMSIPPEVKFNKPFVFLMIEQNTKSPLFMGKVVNPTQK
Fcatus  no alignment    n/a
Mmusculus  partly conserved    384AVLTIDETGTEAAAVTVLQMVPMSMPPILRFDHPFLFIIFEEHTQSPIFLGKVVDPTHK
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 
25418CHAINlost
366381STRANDlost
368392REGIONlost
375418PEPTIDElost
382383SITEReactive bondlost
383383MOD_RESPhosphoserinelost
387389STRANDlost
394400STRANDlost
401403TURNlost
406414STRANDlost
Phylogenetic conservation
PhyloPPhastCons
(flanking)5.3571
5.271
(flanking)-0.3430.234
?
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 14
Strand -1
Original gDNA sequence snippet AGGCTGTGCTGACCATCGACGAGAAAGGGACTGAAGCTGCT
Altered gDNA sequence snippet AGGCTGTGCTGACCATCGACTAGAAAGGGACTGAAGCTGCT
Original cDNA sequence snippet AGGCTGTGCTGACCATCGACGAGAAAGGGACTGAAGCTGCT
Altered cDNA sequence snippet AGGCTGTGCTGACCATCGACTAGAAAGGGACTGAAGCTGCT
Wildtype AA sequence MPSSVSWGIL LLAGLCCLVP VSLAEDPQGD AAQKTDTSHH DQDHPTFNKI TPNLAEFAFS
LYRQLAHQSN STNIFFSPVS IATAFAMLSL GTKADTHDEI LEGLNFNLTE IPEAQIHEGF
QELLRTLNQP DSQLQLTTGN GLFLSEGLKL VDKFLEDVKK LYHSEAFTVN FGDTEEAKKQ
INDYVEKGTQ GKIVDLVKEL DRDTVFALVN YIFFKGKWER PFEVKDTEEE DFHVDQVTTV
KVPMMKRLGM FNIQHCKKLS SWVLLMKYLG NATAIFFLPD EGKLQHLENE LTHDIITKFL
ENEDRRSASL HLPKLSITGT YDLKSVLGQL GITKVFSNGA DLSGVTEEAP LKLSKAVHKA
VLTIDEKGTE AAGAMFLEAI PMSIPPEVKF NKPFVFLMIE QNTKSPLFMG KVVNPTQK*
Mutated AA sequence MPSSVSWGIL LLAGLCCLVP VSLAEDPQGD AAQKTDTSHH DQDHPTFNKI TPNLAEFAFS
LYRQLAHQSN STNIFFSPVS IATAFAMLSL GTKADTHDEI LEGLNFNLTE IPEAQIHEGF
QELLRTLNQP DSQLQLTTGN GLFLSEGLKL VDKFLEDVKK LYHSEAFTVN FGDTEEAKKQ
INDYVEKGTQ GKIVDLVKEL DRDTVFALVN YIFFKGKWER PFEVKDTEEE DFHVDQVTTV
KVPMMKRLGM FNIQHCKKLS SWVLLMKYLG NATAIFFLPD EGKLQHLENE LTHDIITKFL
ENEDRRSASL HLPKLSITGT YDLKSVLGQL GITKVFSNGA DLSGVTEEAP LKLSKAVHKA
VLTID*
Position of stopcodon in wt / mu CDS 1257 / 1098
Position (AA) of stopcodon in wt / mu AA sequence 419 / 366
Position of stopcodon in wt / mu cDNA 1304 / 1145
Position of start ATG in wt / mu cDNA 48 / 48
Last intron/exon boundary 1112
Theoretical NMD boundary in CDS 1014
Length of CDS 1257
Coding sequence (CDS) position 1096
cDNA position 1143
gDNA position 12084
Chromosomal position 94378610
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:

14:94378610C>A_4_ENST00000437397

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
Analysed issue Analysis result
Variant Chr14:94378610C>A (GRCh38)
Gene symbol SERPINA1
Gene constraints LOEUF: 1.13, LOF (oe): 0.79, misssense (oe): 1.02, synonymous (oe): 1.00 ? (gnomAD)
Ensembl transcript ID ENST00000437397.5
Genbank transcript ID NM_001127707 (by similarity), NM_001127706 (by similarity), NM_001127702 (by similarity)
UniProt / AlphaMissense peptide A1AT_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.1096G>T
g.12084G>T
AA changes
AAE:E366*K367-G368-T369-E370-A371-A372-G373-A374-M375-F376-L377-E378-A379-I380-P381-M382-S383-I384-P385-P386-E387-V388-K389-F390-N391-K392-P393-F394-V395-F396-L397-M398-I399-E400-Q401-N402-T403-K404-S405-P406-L407-F408-M409-G410-K411-V412-V413-N414-P415-T416-Q417-K418-*419-?
Score:------------------------------------------------------
Frameshift No
Length of protein Strongly truncated protein, might cause NMD (-53 AA / more than 10% missing)
Pathogenic variant (ClinVar) Variant not listed in ClinVar as (likely) pathogenic.
Variant DBs
Not in dbSNP
gnomADhomozygous (A/A)heterozygousallele carriers
011
Protein conservation
SpeciesMatchGeneAAAlignment
Human      366KAVHKAVLTIDEKGTEAAGAMFLE
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 
25418CHAINlost
366381STRANDlost
368392REGIONlost
375418PEPTIDElost
382383SITEReactive bondlost
383383MOD_RESPhosphoserinelost
387389STRANDlost
394400STRANDlost
401403TURNlost
406414STRANDlost
Phylogenetic conservation
PhyloPPhastCons
(flanking)5.3571
5.271
(flanking)-0.3430.234
?
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 14
Strand -1
Original gDNA sequence snippet AGGCTGTGCTGACCATCGACGAGAAAGGGACTGAAGCTGCT
Altered gDNA sequence snippet AGGCTGTGCTGACCATCGACTAGAAAGGGACTGAAGCTGCT
Original cDNA sequence snippet AGGCTGTGCTGACCATCGACGAGAAAGGGACTGAAGCTGCT
Altered cDNA sequence snippet AGGCTGTGCTGACCATCGACTAGAAAGGGACTGAAGCTGCT
Wildtype AA sequence MPSSVSWGIL LLAGLCCLVP VSLAEDPQGD AAQKTDTSHH DQDHPTFNKI TPNLAEFAFS
LYRQLAHQSN STNIFFSPVS IATAFAMLSL GTKADTHDEI LEGLNFNLTE IPEAQIHEGF
QELLRTLNQP DSQLQLTTGN GLFLSEGLKL VDKFLEDVKK LYHSEAFTVN FGDTEEAKKQ
INDYVEKGTQ GKIVDLVKEL DRDTVFALVN YIFFKGKWER PFEVKDTEEE DFHVDQVTTV
KVPMMKRLGM FNIQHCKKLS SWVLLMKYLG NATAIFFLPD EGKLQHLENE LTHDIITKFL
ENEDRRSASL HLPKLSITGT YDLKSVLGQL GITKVFSNGA DLSGVTEEAP LKLSKAVHKA
VLTIDEKGTE AAGAMFLEAI PMSIPPEVKF NKPFVFLMIE QNTKSPLFMG KVVNPTQK*
Mutated AA sequence MPSSVSWGIL LLAGLCCLVP VSLAEDPQGD AAQKTDTSHH DQDHPTFNKI TPNLAEFAFS
LYRQLAHQSN STNIFFSPVS IATAFAMLSL GTKADTHDEI LEGLNFNLTE IPEAQIHEGF
QELLRTLNQP DSQLQLTTGN GLFLSEGLKL VDKFLEDVKK LYHSEAFTVN FGDTEEAKKQ
INDYVEKGTQ GKIVDLVKEL DRDTVFALVN YIFFKGKWER PFEVKDTEEE DFHVDQVTTV
KVPMMKRLGM FNIQHCKKLS SWVLLMKYLG NATAIFFLPD EGKLQHLENE LTHDIITKFL
ENEDRRSASL HLPKLSITGT YDLKSVLGQL GITKVFSNGA DLSGVTEEAP LKLSKAVHKA
VLTID*
Position of stopcodon in wt / mu CDS 1257 / 1098
Position (AA) of stopcodon in wt / mu AA sequence 419 / 366
Position of stopcodon in wt / mu cDNA 1638 / 1479
Position of start ATG in wt / mu cDNA 382 / 382
Last intron/exon boundary 1446
Theoretical NMD boundary in CDS 1014
Length of CDS 1257
Coding sequence (CDS) position 1096
cDNA position 1477
gDNA position 12084
Chromosomal position 94378610
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:

14:94378610C>A_5_ENST00000448921

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
Analysed issue Analysis result
Variant Chr14:94378610C>A (GRCh38)
Gene symbol SERPINA1
Gene constraints LOEUF: 1.13, LOF (oe): 0.79, misssense (oe): 1.02, synonymous (oe): 1.00 ? (gnomAD)
Ensembl transcript ID ENST00000448921.5
Genbank transcript ID NM_001127704 (by similarity), NM_001127703 (by similarity), NM_001127705 (by similarity), NM_001002236 (by similarity), NM_001127701 (by similarity)
UniProt / AlphaMissense peptide A1AT_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.1096G>T
g.12084G>T
AA changes
AAE:E366*K367-G368-T369-E370-A371-A372-G373-A374-M375-F376-L377-E378-A379-I380-P381-M382-S383-I384-P385-P386-E387-V388-K389-F390-N391-K392-P393-F394-V395-F396-L397-M398-I399-E400-Q401-N402-T403-K404-S405-P406-L407-F408-M409-G410-K411-V412-V413-N414-P415-T416-Q417-K418-*419-?
Score:------------------------------------------------------
Frameshift No
Length of protein Strongly truncated protein, might cause NMD (-53 AA / more than 10% missing)
Pathogenic variant (ClinVar) Variant not listed in ClinVar as (likely) pathogenic.
Variant DBs
Not in dbSNP
gnomADhomozygous (A/A)heterozygousallele carriers
011
Protein conservation
SpeciesMatchGeneAAAlignment
Human      366KAVHKAVLTIDEKGTEAAGAMFLE
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 
25418CHAINlost
366381STRANDlost
368392REGIONlost
375418PEPTIDElost
382383SITEReactive bondlost
383383MOD_RESPhosphoserinelost
387389STRANDlost
394400STRANDlost
401403TURNlost
406414STRANDlost
Phylogenetic conservation
PhyloPPhastCons
(flanking)5.3571
5.271
(flanking)-0.3430.234
?
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 14
Strand -1
Original gDNA sequence snippet AGGCTGTGCTGACCATCGACGAGAAAGGGACTGAAGCTGCT
Altered gDNA sequence snippet AGGCTGTGCTGACCATCGACTAGAAAGGGACTGAAGCTGCT
Original cDNA sequence snippet AGGCTGTGCTGACCATCGACGAGAAAGGGACTGAAGCTGCT
Altered cDNA sequence snippet AGGCTGTGCTGACCATCGACTAGAAAGGGACTGAAGCTGCT
Wildtype AA sequence MPSSVSWGIL LLAGLCCLVP VSLAEDPQGD AAQKTDTSHH DQDHPTFNKI TPNLAEFAFS
LYRQLAHQSN STNIFFSPVS IATAFAMLSL GTKADTHDEI LEGLNFNLTE IPEAQIHEGF
QELLRTLNQP DSQLQLTTGN GLFLSEGLKL VDKFLEDVKK LYHSEAFTVN FGDTEEAKKQ
INDYVEKGTQ GKIVDLVKEL DRDTVFALVN YIFFKGKWER PFEVKDTEEE DFHVDQVTTV
KVPMMKRLGM FNIQHCKKLS SWVLLMKYLG NATAIFFLPD EGKLQHLENE LTHDIITKFL
ENEDRRSASL HLPKLSITGT YDLKSVLGQL GITKVFSNGA DLSGVTEEAP LKLSKAVHKA
VLTIDEKGTE AAGAMFLEAI PMSIPPEVKF NKPFVFLMIE QNTKSPLFMG KVVNPTQK*
Mutated AA sequence MPSSVSWGIL LLAGLCCLVP VSLAEDPQGD AAQKTDTSHH DQDHPTFNKI TPNLAEFAFS
LYRQLAHQSN STNIFFSPVS IATAFAMLSL GTKADTHDEI LEGLNFNLTE IPEAQIHEGF
QELLRTLNQP DSQLQLTTGN GLFLSEGLKL VDKFLEDVKK LYHSEAFTVN FGDTEEAKKQ
INDYVEKGTQ GKIVDLVKEL DRDTVFALVN YIFFKGKWER PFEVKDTEEE DFHVDQVTTV
KVPMMKRLGM FNIQHCKKLS SWVLLMKYLG NATAIFFLPD EGKLQHLENE LTHDIITKFL
ENEDRRSASL HLPKLSITGT YDLKSVLGQL GITKVFSNGA DLSGVTEEAP LKLSKAVHKA
VLTID*
Position of stopcodon in wt / mu CDS 1257 / 1098
Position (AA) of stopcodon in wt / mu AA sequence 419 / 366
Position of stopcodon in wt / mu cDNA 1830 / 1671
Position of start ATG in wt / mu cDNA 574 / 574
Last intron/exon boundary 1638
Theoretical NMD boundary in CDS 1014
Length of CDS 1257
Coding sequence (CDS) position 1096
cDNA position 1669
gDNA position 12084
Chromosomal position 94378610
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:

14:94378610C>A_6_ENST00000636712

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
Analysed issue Analysis result
Variant Chr14:94378610C>A (GRCh38)
Gene symbol SERPINA1
Gene constraints LOEUF: 1.13, LOF (oe): 0.79, misssense (oe): 1.02, synonymous (oe): 1.00 ? (gnomAD)
Ensembl transcript ID ENST00000636712.1
Genbank transcript ID
UniProt / AlphaMissense peptide A1AT_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.1096G>T
g.12084G>T
AA changes
AAE:E366*K367-G368-T369-E370-A371-A372-G373-A374-M375-F376-L377-E378-A379-I380-P381-M382-S383-I384-P385-P386-E387-V388-K389-F390-N391-K392-P393-F394-V395-F396-L397-M398-I399-E400-Q401-N402-T403-K404-S405-P406-L407-F408-M409-G410-K411-V412-V413-N414-P415-T416-Q417-K418-*419-?
Score:------------------------------------------------------
Frameshift No
Length of protein Strongly truncated protein, might cause NMD (-53 AA / more than 10% missing)
Pathogenic variant (ClinVar) Variant not listed in ClinVar as (likely) pathogenic.
Variant DBs
Not in dbSNP
gnomADhomozygous (A/A)heterozygousallele carriers
011
Protein conservation
SpeciesMatchGeneAAAlignment
Human      366KAVHKAVLTIDEKGTEAAGAMFLE
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 
25418CHAINlost
366381STRANDlost
368392REGIONlost
375418PEPTIDElost
382383SITEReactive bondlost
383383MOD_RESPhosphoserinelost
387389STRANDlost
394400STRANDlost
401403TURNlost
406414STRANDlost
Phylogenetic conservation
PhyloPPhastCons
(flanking)5.3571
5.271
(flanking)-0.3430.234
?
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 14
Strand -1
Original gDNA sequence snippet AGGCTGTGCTGACCATCGACGAGAAAGGGACTGAAGCTGCT
Altered gDNA sequence snippet AGGCTGTGCTGACCATCGACTAGAAAGGGACTGAAGCTGCT
Original cDNA sequence snippet AGGCTGTGCTGACCATCGACGAGAAAGGGACTGAAGCTGCT
Altered cDNA sequence snippet AGGCTGTGCTGACCATCGACTAGAAAGGGACTGAAGCTGCT
Wildtype AA sequence MPSSVSWGIL LLAGLCCLVP VSLAEDPQGD AAQKTDTSHH DQDHPTFNKI TPNLAEFAFS
LYRQLAHQSN STNIFFSPVS IATAFAMLSL GTKADTHDEI LEGLNFNLTE IPEAQIHEGF
QELLRTLNQP DSQLQLTTGN GLFLSEGLKL VDKFLEDVKK LYHSEAFTVN FGDTEEAKKQ
INDYVEKGTQ GKIVDLVKEL DRDTVFALVN YIFFKGKWER PFEVKDTEEE DFHVDQVTTV
KVPMMKRLGM FNIQHCKKLS SWVLLMKYLG NATAIFFLPD EGKLQHLENE LTHDIITKFL
ENEDRRSASL HLPKLSITGT YDLKSVLGQL GITKVFSNGA DLSGVTEEAP LKLSKAVHKA
VLTIDEKGTE AAGAMFLEAI PMSIPPEVKF NKPFVFLMIE QNTKSPLFMG KVVNPTQK*
Mutated AA sequence MPSSVSWGIL LLAGLCCLVP VSLAEDPQGD AAQKTDTSHH DQDHPTFNKI TPNLAEFAFS
LYRQLAHQSN STNIFFSPVS IATAFAMLSL GTKADTHDEI LEGLNFNLTE IPEAQIHEGF
QELLRTLNQP DSQLQLTTGN GLFLSEGLKL VDKFLEDVKK LYHSEAFTVN FGDTEEAKKQ
INDYVEKGTQ GKIVDLVKEL DRDTVFALVN YIFFKGKWER PFEVKDTEEE DFHVDQVTTV
KVPMMKRLGM FNIQHCKKLS SWVLLMKYLG NATAIFFLPD EGKLQHLENE LTHDIITKFL
ENEDRRSASL HLPKLSITGT YDLKSVLGQL GITKVFSNGA DLSGVTEEAP LKLSKAVHKA
VLTID*
Position of stopcodon in wt / mu CDS 1257 / 1098
Position (AA) of stopcodon in wt / mu AA sequence 419 / 366
Position of stopcodon in wt / mu cDNA 1409 / 1250
Position of start ATG in wt / mu cDNA 153 / 153
Last intron/exon boundary 1217
Theoretical NMD boundary in CDS 1014
Length of CDS 1257
Coding sequence (CDS) position 1096
cDNA position 1248
gDNA position 12084
Chromosomal position 94378610
Speed 0.09 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:

14:94378610C>A_7_ENST00000393088

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
Analysed issue Analysis result
Variant Chr14:94378610C>A (GRCh38)
Gene symbol SERPINA1
Gene constraints LOEUF: 1.13, LOF (oe): 0.79, misssense (oe): 1.02, synonymous (oe): 1.00 ? (gnomAD)
Ensembl transcript ID ENST00000393088.8
Genbank transcript ID
UniProt / AlphaMissense peptide A1AT_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.1096G>T
g.12084G>T
AA changes
AAE:E366*K367-G368-T369-E370-A371-A372-G373-A374-M375-F376-L377-E378-A379-I380-P381-M382-S383-I384-P385-P386-E387-V388-K389-F390-N391-K392-P393-F394-V395-F396-L397-M398-I399-E400-Q401-N402-T403-K404-S405-P406-L407-F408-M409-G410-K411-V412-V413-N414-P415-T416-Q417-K418-*419-?
Score:------------------------------------------------------
Frameshift No
Length of protein Strongly truncated protein, might cause NMD (-53 AA / more than 10% missing)
Pathogenic variant (ClinVar) Variant not listed in ClinVar as (likely) pathogenic.
Variant DBs
Not in dbSNP
gnomADhomozygous (A/A)heterozygousallele carriers
011
Protein conservation
SpeciesMatchGeneAAAlignment
Human      366KAVHKAVLTIDEKGTEAAGAMFLE
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 
25418CHAINlost
366381STRANDlost
368392REGIONlost
375418PEPTIDElost
382383SITEReactive bondlost
383383MOD_RESPhosphoserinelost
387389STRANDlost
394400STRANDlost
401403TURNlost
406414STRANDlost
Phylogenetic conservation
PhyloPPhastCons
(flanking)5.3571
5.271
(flanking)-0.3430.234
?
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 14
Strand -1
Original gDNA sequence snippet AGGCTGTGCTGACCATCGACGAGAAAGGGACTGAAGCTGCT
Altered gDNA sequence snippet AGGCTGTGCTGACCATCGACTAGAAAGGGACTGAAGCTGCT
Original cDNA sequence snippet AGGCTGTGCTGACCATCGACGAGAAAGGGACTGAAGCTGCT
Altered cDNA sequence snippet AGGCTGTGCTGACCATCGACTAGAAAGGGACTGAAGCTGCT
Wildtype AA sequence MPSSVSWGIL LLAGLCCLVP VSLAEDPQGD AAQKTDTSHH DQDHPTFNKI TPNLAEFAFS
LYRQLAHQSN STNIFFSPVS IATAFAMLSL GTKADTHDEI LEGLNFNLTE IPEAQIHEGF
QELLRTLNQP DSQLQLTTGN GLFLSEGLKL VDKFLEDVKK LYHSEAFTVN FGDTEEAKKQ
INDYVEKGTQ GKIVDLVKEL DRDTVFALVN YIFFKGKWER PFEVKDTEEE DFHVDQVTTV
KVPMMKRLGM FNIQHCKKLS SWVLLMKYLG NATAIFFLPD EGKLQHLENE LTHDIITKFL
ENEDRRSASL HLPKLSITGT YDLKSVLGQL GITKVFSNGA DLSGVTEEAP LKLSKAVHKA
VLTIDEKGTE AAGAMFLEAI PMSIPPEVKF NKPFVFLMIE QNTKSPLFMG KVVNPTQK*
Mutated AA sequence MPSSVSWGIL LLAGLCCLVP VSLAEDPQGD AAQKTDTSHH DQDHPTFNKI TPNLAEFAFS
LYRQLAHQSN STNIFFSPVS IATAFAMLSL GTKADTHDEI LEGLNFNLTE IPEAQIHEGF
QELLRTLNQP DSQLQLTTGN GLFLSEGLKL VDKFLEDVKK LYHSEAFTVN FGDTEEAKKQ
INDYVEKGTQ GKIVDLVKEL DRDTVFALVN YIFFKGKWER PFEVKDTEEE DFHVDQVTTV
KVPMMKRLGM FNIQHCKKLS SWVLLMKYLG NATAIFFLPD EGKLQHLENE LTHDIITKFL
ENEDRRSASL HLPKLSITGT YDLKSVLGQL GITKVFSNGA DLSGVTEEAP LKLSKAVHKA
VLTID*
Position of stopcodon in wt / mu CDS 1257 / 1098
Position (AA) of stopcodon in wt / mu AA sequence 419 / 366
Position of stopcodon in wt / mu cDNA 1812 / 1653
Position of start ATG in wt / mu cDNA 556 / 556
Last intron/exon boundary 1620
Theoretical NMD boundary in CDS 1014
Length of CDS 1257
Coding sequence (CDS) position 1096
cDNA position 1651
gDNA position 12084
Chromosomal position 94378610
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:

14:94378610C>A_8_ENST00000404814

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
Analysed issue Analysis result
Variant Chr14:94378610C>A (GRCh38)
Gene symbol SERPINA1
Gene constraints LOEUF: 1.13, LOF (oe): 0.79, misssense (oe): 1.02, synonymous (oe): 1.00 ? (gnomAD)
Ensembl transcript ID ENST00000404814.8
Genbank transcript ID
UniProt / AlphaMissense peptide A1AT_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.1096G>T
g.12084G>T
AA changes
AAE:E366*K367-G368-T369-E370-A371-A372-G373-A374-M375-F376-L377-E378-A379-I380-P381-M382-S383-I384-P385-P386-E387-V388-K389-F390-N391-K392-P393-F394-V395-F396-L397-M398-I399-E400-Q401-N402-T403-K404-S405-P406-L407-F408-M409-G410-K411-V412-V413-N414-P415-T416-Q417-K418-*419-?
Score:------------------------------------------------------
Frameshift No
Length of protein Strongly truncated protein, might cause NMD (-53 AA / more than 10% missing)
Pathogenic variant (ClinVar) Variant not listed in ClinVar as (likely) pathogenic.
Variant DBs
Not in dbSNP
gnomADhomozygous (A/A)heterozygousallele carriers
011
Protein conservation
SpeciesMatchGeneAAAlignment
Human      366KAVHKAVLTIDEKGTEAAGAMFLE
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 
25418CHAINlost
366381STRANDlost
368392REGIONlost
375418PEPTIDElost
382383SITEReactive bondlost
383383MOD_RESPhosphoserinelost
387389STRANDlost
394400STRANDlost
401403TURNlost
406414STRANDlost
Phylogenetic conservation
PhyloPPhastCons
(flanking)5.3571
5.271
(flanking)-0.3430.234
?
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 14
Strand -1
Original gDNA sequence snippet AGGCTGTGCTGACCATCGACGAGAAAGGGACTGAAGCTGCT
Altered gDNA sequence snippet AGGCTGTGCTGACCATCGACTAGAAAGGGACTGAAGCTGCT
Original cDNA sequence snippet AGGCTGTGCTGACCATCGACGAGAAAGGGACTGAAGCTGCT
Altered cDNA sequence snippet AGGCTGTGCTGACCATCGACTAGAAAGGGACTGAAGCTGCT
Wildtype AA sequence MPSSVSWGIL LLAGLCCLVP VSLAEDPQGD AAQKTDTSHH DQDHPTFNKI TPNLAEFAFS
LYRQLAHQSN STNIFFSPVS IATAFAMLSL GTKADTHDEI LEGLNFNLTE IPEAQIHEGF
QELLRTLNQP DSQLQLTTGN GLFLSEGLKL VDKFLEDVKK LYHSEAFTVN FGDTEEAKKQ
INDYVEKGTQ GKIVDLVKEL DRDTVFALVN YIFFKGKWER PFEVKDTEEE DFHVDQVTTV
KVPMMKRLGM FNIQHCKKLS SWVLLMKYLG NATAIFFLPD EGKLQHLENE LTHDIITKFL
ENEDRRSASL HLPKLSITGT YDLKSVLGQL GITKVFSNGA DLSGVTEEAP LKLSKAVHKA
VLTIDEKGTE AAGAMFLEAI PMSIPPEVKF NKPFVFLMIE QNTKSPLFMG KVVNPTQK*
Mutated AA sequence MPSSVSWGIL LLAGLCCLVP VSLAEDPQGD AAQKTDTSHH DQDHPTFNKI TPNLAEFAFS
LYRQLAHQSN STNIFFSPVS IATAFAMLSL GTKADTHDEI LEGLNFNLTE IPEAQIHEGF
QELLRTLNQP DSQLQLTTGN GLFLSEGLKL VDKFLEDVKK LYHSEAFTVN FGDTEEAKKQ
INDYVEKGTQ GKIVDLVKEL DRDTVFALVN YIFFKGKWER PFEVKDTEEE DFHVDQVTTV
KVPMMKRLGM FNIQHCKKLS SWVLLMKYLG NATAIFFLPD EGKLQHLENE LTHDIITKFL
ENEDRRSASL HLPKLSITGT YDLKSVLGQL GITKVFSNGA DLSGVTEEAP LKLSKAVHKA
VLTID*
Position of stopcodon in wt / mu CDS 1257 / 1098
Position (AA) of stopcodon in wt / mu AA sequence 419 / 366
Position of stopcodon in wt / mu cDNA 1568 / 1409
Position of start ATG in wt / mu cDNA 312 / 312
Last intron/exon boundary 1376
Theoretical NMD boundary in CDS 1014
Length of CDS 1257
Coding sequence (CDS) position 1096
cDNA position 1407
gDNA position 12084
Chromosomal position 94378610
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:

14:94378610C>A_9_ENST00000449399

Back to summary table

Prediction:

DeleteriousPermalink

Summary:

  • Model: complex_aae
  • Tree vote: 10|0 (del | benign) ?
Analysed issue Analysis result
Variant Chr14:94378610C>A (GRCh38)
Gene symbol SERPINA1
Gene constraints LOEUF: 1.13, LOF (oe): 0.79, misssense (oe): 1.02, synonymous (oe): 1.00 ? (gnomAD)
Ensembl transcript ID ENST00000449399.7
Genbank transcript ID
UniProt / AlphaMissense peptide A1AT_HUMAN | AlphaMissense: transcript, gene
Variant type Single base exchange
Gene region CDS
DNA changes c.1096G>T
g.12084G>T
AA changes
AAE:E366*K367-G368-T369-E370-A371-A372-G373-A374-M375-F376-L377-E378-A379-I380-P381-M382-S383-I384-P385-P386-E387-V388-K389-F390-N391-K392-P393-F394-V395-F396-L397-M398-I399-E400-Q401-N402-T403-K404-S405-P406-L407-F408-M409-G410-K411-V412-V413-N414-P415-T416-Q417-K418-*419-?
Score:------------------------------------------------------
Frameshift No
Length of protein Strongly truncated protein, might cause NMD (-53 AA / more than 10% missing)
Pathogenic variant (ClinVar) Variant not listed in ClinVar as (likely) pathogenic.
Variant DBs
Not in dbSNP
gnomADhomozygous (A/A)heterozygousallele carriers
011
Protein conservation
SpeciesMatchGeneAAAlignment
Human      366KAVHKAVLTIDEKGTEAAGAMFLE
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 
25418CHAINlost
366381STRANDlost
368392REGIONlost
375418PEPTIDElost
382383SITEReactive bondlost
383383MOD_RESPhosphoserinelost
387389STRANDlost
394400STRANDlost
401403TURNlost
406414STRANDlost
Phylogenetic conservation
PhyloPPhastCons
(flanking)5.3571
5.271
(flanking)-0.3430.234
?
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 14
Strand -1
Original gDNA sequence snippet AGGCTGTGCTGACCATCGACGAGAAAGGGACTGAAGCTGCT
Altered gDNA sequence snippet AGGCTGTGCTGACCATCGACTAGAAAGGGACTGAAGCTGCT
Original cDNA sequence snippet AGGCTGTGCTGACCATCGACGAGAAAGGGACTGAAGCTGCT
Altered cDNA sequence snippet AGGCTGTGCTGACCATCGACTAGAAAGGGACTGAAGCTGCT
Wildtype AA sequence MPSSVSWGIL LLAGLCCLVP VSLAEDPQGD AAQKTDTSHH DQDHPTFNKI TPNLAEFAFS
LYRQLAHQSN STNIFFSPVS IATAFAMLSL GTKADTHDEI LEGLNFNLTE IPEAQIHEGF
QELLRTLNQP DSQLQLTTGN GLFLSEGLKL VDKFLEDVKK LYHSEAFTVN FGDTEEAKKQ
INDYVEKGTQ GKIVDLVKEL DRDTVFALVN YIFFKGKWER PFEVKDTEEE DFHVDQVTTV
KVPMMKRLGM FNIQHCKKLS SWVLLMKYLG NATAIFFLPD EGKLQHLENE LTHDIITKFL
ENEDRRSASL HLPKLSITGT YDLKSVLGQL GITKVFSNGA DLSGVTEEAP LKLSKAVHKA
VLTIDEKGTE AAGAMFLEAI PMSIPPEVKF NKPFVFLMIE QNTKSPLFMG KVVNPTQK*
Mutated AA sequence MPSSVSWGIL LLAGLCCLVP VSLAEDPQGD AAQKTDTSHH DQDHPTFNKI TPNLAEFAFS
LYRQLAHQSN STNIFFSPVS IATAFAMLSL GTKADTHDEI LEGLNFNLTE IPEAQIHEGF
QELLRTLNQP DSQLQLTTGN GLFLSEGLKL VDKFLEDVKK LYHSEAFTVN FGDTEEAKKQ
INDYVEKGTQ GKIVDLVKEL DRDTVFALVN YIFFKGKWER PFEVKDTEEE DFHVDQVTTV
KVPMMKRLGM FNIQHCKKLS SWVLLMKYLG NATAIFFLPD EGKLQHLENE LTHDIITKFL
ENEDRRSASL HLPKLSITGT YDLKSVLGQL GITKVFSNGA DLSGVTEEAP LKLSKAVHKA
VLTID*
Position of stopcodon in wt / mu CDS 1257 / 1098
Position (AA) of stopcodon in wt / mu AA sequence 419 / 366
Position of stopcodon in wt / mu cDNA 1559 / 1400
Position of start ATG in wt / mu cDNA 303 / 303
Last intron/exon boundary 1367
Theoretical NMD boundary in CDS 1014
Length of CDS 1257
Coding sequence (CDS) position 1096
cDNA position 1398
gDNA position 12084
Chromosomal position 94378610
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