Yum, tasty mutations...

MutationTaster - study a chromosomal position

 MTQE documentation
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...
found 4 transcript(s)...
Querying Taster for transcript #1: ENST00000357578
Querying Taster for transcript #2: ENST00000491546
Querying Taster for transcript #3: ENST00000348925
Querying Taster for transcript #4: ENST00000546278
MT speed 0 s - this script 4.780795 s

Results

genesymbolpredictionprobabilitymodelprediction
problem		splicingClinVaramino acid changesvariant typedbSNP IDprotein lengthfile
ALDH5A1disease_causing_automatic0.999999999995608simple_aaeaffected0G409Dsingle base exchangers118203984show file
ALDH5A1disease_causing_automatic0.999999999995608simple_aaeaffected0G381Dsingle base exchangers118203984show file
ALDH5A1disease_causing_automatic0.999999999995608simple_aaeaffected0G422Dsingle base exchangers118203984show file
ALDH5A1disease_causing_automatic0.999999999999279simple_aaeaffected0G321Dsingle base exchangers118203984show file

Taster files

Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999999995608 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM012724)
  • known disease mutation: rs1359 (pathogenic)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr6:24528277G>AN/A show variant in all transcripts   IGV
HGNC symbol ALDH5A1
Ensembl transcript ID ENST00000357578
Genbank transcript ID NM_001080
UniProt peptide P51649
alteration type single base exchange
alteration region CDS
DNA changes c.1226G>A
cDNA.1371G>A
g.33198G>A
AA changes G409D Score: 94 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 409
frameshift no
known variant Reference ID: rs118203984
databasehomozygous (A/A)heterozygousallele carriers
1000G---
ExAC066

known disease mutation: rs1359 (pathogenic for Succinate-semialdehyde dehydrogenase deficiency) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM012724)

known disease mutation at this position, please check HGMD for details (HGMD ID CM012724)
known disease mutation at this position, please check HGMD for details (HGMD ID CM012724)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)5.8071
5.8071
(flanking)-0.6230.774
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor increased33200wt: 0.49 / mu: 0.91wt: CAGGTGGAAAACGAC
mu: CAGATGGAAAACGAC		 GGTG|gaaa
Donor increased33199wt: 0.34 / mu: 0.81wt: ACAGGTGGAAAACGA
mu: ACAGATGGAAAACGA		 AGGT|ggaa
Donor gained331940.59mu: TTGTGACAGATGGAA GTGA|caga
distance from splice site 53
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      409DAVSKGATVVTGGKRHQLGKNFFE
mutated  not conserved    409DAVSKGATVVTDGKRHQLGKNFF
Ptroglodytes  all identical  ENSPTRG00000017776  409DAVSKGATVVTGGKRHQLGKNFF
Mmulatta  all identical  ENSMMUG00000019368  422TGGKRHHLGKNFF
Fcatus  all identical  ENSFCAG00000011094  304VVTGGKRHQLGKNFF
Mmusculus  all identical  ENSMUSG00000035936  397DAVAKGATVVTGGKRHQSGGNFF
Ggallus  all identical  ENSGALG00000012663  390DAVSQGASVVTGGKRHSLGKNFF
Trubripes  no homologue    
Drerio  all identical  ENSDARG00000076544  389DAVDHGAVVVRGGKR-
Dmelanogaster  all identical  FBgn0039349  379NIILGGQPLPDKGSLFY
Celegans  all identical  F45H10.1  369DALGKGSELICGGKRGEHGTS-
Xtropicalis  all identical  ENSXETG00000021961  362NAVSLGAQIEAGGKRSAVGKNFF
protein features
start (aa)end (aa)featuredetails 
405408STRANDmight get lost (downstream of altered splice site)
423428STRANDmight get lost (downstream of altered splice site)
430433HELIXmight get lost (downstream of altered splice site)
441450STRANDmight get lost (downstream of altered splice site)
452459HELIXmight get lost (downstream of altered splice site)
466471STRANDmight get lost (downstream of altered splice site)
475484HELIXmight get lost (downstream of altered splice site)
487493STRANDmight get lost (downstream of altered splice site)
498498BINDINGSubstrate.might get lost (downstream of altered splice site)
498498MUTAGENS->A: Reduces catalytic activity to less than 15% of wild-type.might get lost (downstream of altered splice site)
508510HELIXmight get lost (downstream of altered splice site)
511513STRANDmight get lost (downstream of altered splice site)
517519TURNmight get lost (downstream of altered splice site)
520524HELIXmight get lost (downstream of altered splice site)
525532STRANDmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1608 / 1608
position (AA) of stopcodon in wt / mu AA sequence 536 / 536
position of stopcodon in wt / mu cDNA 1753 / 1753
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 146 / 146
chromosome 6
strand 1
last intron/exon boundary 1548
theoretical NMD boundary in CDS 1352
length of CDS 1608
coding sequence (CDS) position 1226
cDNA position
(for ins/del: last normal base / first normal base)		 1371
gDNA position
(for ins/del: last normal base / first normal base)		 33198
chromosomal position
(for ins/del: last normal base / first normal base)		 24528277
original gDNA sequence snippet AGGTGCCACCGTTGTGACAGGTGGAAAACGACACCAACTTG
altered gDNA sequence snippet AGGTGCCACCGTTGTGACAGATGGAAAACGACACCAACTTG
original cDNA sequence snippet AGGTGCCACCGTTGTGACAGGTGGAAAACGACACCAACTTG
altered cDNA sequence snippet AGGTGCCACCGTTGTGACAGATGGAAAACGACACCAACTTG
wildtype AA sequence MATCIWLRSC GARRLGSTFP GCRLRPRAGG LVPASGPAPG PAQLRCYAGR LAGLSAALLR
TDSFVGGRWL PAAATFPVQD PASGAALGMV ADCGVREARA AVRAAYEAFC RWREVSAKER
SSLLRKWYNL MIQNKDDLAR IITAESGKPL KEAHGEILYS AFFLEWFSEE ARRVYGDIIH
TPAKDRRALV LKQPIGVAAV ITPWNFPSAM ITRKVGAALA AGCTVVVKPA EDTPFSALAL
AELASQAGIP SGVYNVIPCS RKNAKEVGEA ICTDPLVSKI SFTGSTTTGK ILLHHAANSV
KRVSMELGGL APFIVFDSAN VDQAVAGAMA SKFRNTGQTC VCSNQFLVQR GIHDAFVKAF
AEAMKKNLRV GNGFEEGTTQ GPLINEKAVE KVEKQVNDAV SKGATVVTGG KRHQLGKNFF
EPTLLCNVTQ DMLCTHEETF GPLAPVIKFD TEEEAIAIAN AADVGLAGYF YSQDPAQIWR
VAEQLEVGMV GVNEGLISSV ECPFGGVKQS GLGREGSKYG IDEYLELKYV CYGGL*
mutated AA sequence MATCIWLRSC GARRLGSTFP GCRLRPRAGG LVPASGPAPG PAQLRCYAGR LAGLSAALLR
TDSFVGGRWL PAAATFPVQD PASGAALGMV ADCGVREARA AVRAAYEAFC RWREVSAKER
SSLLRKWYNL MIQNKDDLAR IITAESGKPL KEAHGEILYS AFFLEWFSEE ARRVYGDIIH
TPAKDRRALV LKQPIGVAAV ITPWNFPSAM ITRKVGAALA AGCTVVVKPA EDTPFSALAL
AELASQAGIP SGVYNVIPCS RKNAKEVGEA ICTDPLVSKI SFTGSTTTGK ILLHHAANSV
KRVSMELGGL APFIVFDSAN VDQAVAGAMA SKFRNTGQTC VCSNQFLVQR GIHDAFVKAF
AEAMKKNLRV GNGFEEGTTQ GPLINEKAVE KVEKQVNDAV SKGATVVTDG KRHQLGKNFF
EPTLLCNVTQ DMLCTHEETF GPLAPVIKFD TEEEAIAIAN AADVGLAGYF YSQDPAQIWR
VAEQLEVGMV GVNEGLISSV ECPFGGVKQS GLGREGSKYG IDEYLELKYV CYGGL*
speed 1.04 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
back to results table
Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999999995608 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM012724)
  • known disease mutation: rs1359 (pathogenic)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr6:24528277G>AN/A show variant in all transcripts   IGV
HGNC symbol ALDH5A1
Ensembl transcript ID ENST00000491546
Genbank transcript ID N/A
UniProt peptide P51649
alteration type single base exchange
alteration region CDS
DNA changes c.1142G>A
cDNA.1272G>A
g.33198G>A
AA changes G381D Score: 94 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 381
frameshift no
known variant Reference ID: rs118203984
databasehomozygous (A/A)heterozygousallele carriers
1000G---
ExAC066

known disease mutation: rs1359 (pathogenic for Succinate-semialdehyde dehydrogenase deficiency) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM012724)

known disease mutation at this position, please check HGMD for details (HGMD ID CM012724)
known disease mutation at this position, please check HGMD for details (HGMD ID CM012724)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)5.8071
5.8071
(flanking)-0.6230.774
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor increased33200wt: 0.49 / mu: 0.91wt: CAGGTGGAAAACGAC
mu: CAGATGGAAAACGAC		 GGTG|gaaa
Donor increased33199wt: 0.34 / mu: 0.81wt: ACAGGTGGAAAACGA
mu: ACAGATGGAAAACGA		 AGGT|ggaa
Donor gained331940.59mu: TTGTGACAGATGGAA GTGA|caga
distance from splice site 53
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      381DAVSKGATVVTGGKRHQLGKNFFE
mutated  not conserved    381DAVSKGATVVTDGKRHQLGKNFF
Ptroglodytes  all identical  ENSPTRG00000017776  409DAVSKGATVVTGGKRHQLGKNFF
Mmulatta  all identical  ENSMMUG00000019368  422TGGKRHHLGKNFF
Fcatus  all identical  ENSFCAG00000011094  304DAVSKGATVVTGGKRHQLGKNFF
Mmusculus  all identical  ENSMUSG00000035936  397DAVAKGATVVTGGKRHQSGGNFF
Ggallus  all identical  ENSGALG00000012663  390DAVSQGASVVTGGKRHSLGKNFF
Trubripes  no homologue    
Drerio  all identical  ENSDARG00000076544  389DAVDHGAVVVRGGKR-
Dmelanogaster  all identical  FBgn0039349  379NIILGGQPLPDKGSLFY
Celegans  all identical  F45H10.1  369DALGKGSELICGGKRGEHGTS-
Xtropicalis  all identical  ENSXETG00000021961  362NAVSLGAQIEAGGKRSAVGKNFF
protein features
start (aa)end (aa)featuredetails 
386400HELIXmight get lost (downstream of altered splice site)
401403TURNmight get lost (downstream of altered splice site)
405408STRANDmight get lost (downstream of altered splice site)
423428STRANDmight get lost (downstream of altered splice site)
430433HELIXmight get lost (downstream of altered splice site)
441450STRANDmight get lost (downstream of altered splice site)
452459HELIXmight get lost (downstream of altered splice site)
466471STRANDmight get lost (downstream of altered splice site)
475484HELIXmight get lost (downstream of altered splice site)
487493STRANDmight get lost (downstream of altered splice site)
498498BINDINGSubstrate.might get lost (downstream of altered splice site)
498498MUTAGENS->A: Reduces catalytic activity to less than 15% of wild-type.might get lost (downstream of altered splice site)
508510HELIXmight get lost (downstream of altered splice site)
511513STRANDmight get lost (downstream of altered splice site)
517519TURNmight get lost (downstream of altered splice site)
520524HELIXmight get lost (downstream of altered splice site)
525532STRANDmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1524 / 1524
position (AA) of stopcodon in wt / mu AA sequence 508 / 508
position of stopcodon in wt / mu cDNA 1654 / 1654
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 131 / 131
chromosome 6
strand 1
last intron/exon boundary 1449
theoretical NMD boundary in CDS 1268
length of CDS 1524
coding sequence (CDS) position 1142
cDNA position
(for ins/del: last normal base / first normal base)		 1272
gDNA position
(for ins/del: last normal base / first normal base)		 33198
chromosomal position
(for ins/del: last normal base / first normal base)		 24528277
original gDNA sequence snippet AGGTGCCACCGTTGTGACAGGTGGAAAACGACACCAACTTG
altered gDNA sequence snippet AGGTGCCACCGTTGTGACAGATGGAAAACGACACCAACTTG
original cDNA sequence snippet AGGTGCCACCGTTGTGACAGGTGGAAAACGACACCAACTTG
altered cDNA sequence snippet AGGTGCCACCGTTGTGACAGATGGAAAACGACACCAACTTG
wildtype AA sequence MATCIWLRSC GARRLGSTFP GCRLRPRAGG LVPASGPAPG PAQLRCYAGR LAGLSAALLR
TDSFVGGRWL PAAATFPVQD PASGAALGMV ADCGVREARA AVRAAYEAFC RWREVSAKGK
PLKEAHGEIL YSAFFLEWFS EEARRVYGDI IHTPAKDRRA LVLKQPIGVA AVITPWNFPS
AMITRKVGAA LAAGCTVVVK PAEDTPFSAL ALAELASQAG IPSGVYNVIP CSRKNAKEVG
EAICTDPLVS KISFTGSTTT GKILLHHAAN SVKRVSMELG GLAPFIVFDS ANVDQAVAGA
MASKFRNTGQ TCVCSNQFLV QRGIHDAFVK AFAEAMKKNL RVGNGFEEGT TQGPLINEKA
VEKVEKQVND AVSKGATVVT GGKRHQLGKN FFEPTLLCNV TQDMLCTHEE TFGPLAPVIK
FDTEEEAIAI ANAADVGLAG YFYSQDPAQI WRVAEQLEVG MVGVNEGLIS SVECPFGGVK
QSGLGREGSK YGIDEYLELK YVCYGGL*
mutated AA sequence MATCIWLRSC GARRLGSTFP GCRLRPRAGG LVPASGPAPG PAQLRCYAGR LAGLSAALLR
TDSFVGGRWL PAAATFPVQD PASGAALGMV ADCGVREARA AVRAAYEAFC RWREVSAKGK
PLKEAHGEIL YSAFFLEWFS EEARRVYGDI IHTPAKDRRA LVLKQPIGVA AVITPWNFPS
AMITRKVGAA LAAGCTVVVK PAEDTPFSAL ALAELASQAG IPSGVYNVIP CSRKNAKEVG
EAICTDPLVS KISFTGSTTT GKILLHHAAN SVKRVSMELG GLAPFIVFDS ANVDQAVAGA
MASKFRNTGQ TCVCSNQFLV QRGIHDAFVK AFAEAMKKNL RVGNGFEEGT TQGPLINEKA
VEKVEKQVND AVSKGATVVT DGKRHQLGKN FFEPTLLCNV TQDMLCTHEE TFGPLAPVIK
FDTEEEAIAI ANAADVGLAG YFYSQDPAQI WRVAEQLEVG MVGVNEGLIS SVECPFGGVK
QSGLGREGSK YGIDEYLELK YVCYGGL*
speed 1.06 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
back to results table
Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999999995608 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM012724)
  • known disease mutation: rs1359 (pathogenic)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr6:24528277G>AN/A show variant in all transcripts   IGV
HGNC symbol ALDH5A1
Ensembl transcript ID ENST00000348925
Genbank transcript ID NM_170740
UniProt peptide P51649
alteration type single base exchange
alteration region CDS
DNA changes c.1265G>A
cDNA.1293G>A
g.33198G>A
AA changes G422D Score: 94 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 422
frameshift no
known variant Reference ID: rs118203984
databasehomozygous (A/A)heterozygousallele carriers
1000G---
ExAC066

known disease mutation: rs1359 (pathogenic for Succinate-semialdehyde dehydrogenase deficiency) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM012724)

known disease mutation at this position, please check HGMD for details (HGMD ID CM012724)
known disease mutation at this position, please check HGMD for details (HGMD ID CM012724)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)5.8071
5.8071
(flanking)-0.6230.774
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor increased33200wt: 0.49 / mu: 0.91wt: CAGGTGGAAAACGAC
mu: CAGATGGAAAACGAC		 GGTG|gaaa
Donor increased33199wt: 0.34 / mu: 0.81wt: ACAGGTGGAAAACGA
mu: ACAGATGGAAAACGA		 AGGT|ggaa
Donor gained331940.59mu: TTGTGACAGATGGAA GTGA|caga
distance from splice site 53
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      422DAVSKGATVVTGGKRHQLGKNFFE
mutated  not conserved    422TDGKRHQLGKNFF
Ptroglodytes  all identical  ENSPTRG00000017776  409TGGKRHQLGKNFF
Mmulatta  all identical  ENSMMUG00000019368  422TGGKRHHLGKNFF
Fcatus  all identical  ENSFCAG00000011094  304VVTGGKRHQLGKNFF
Mmusculus  all identical  ENSMUSG00000035936  397TGGKRHQSGGNFF
Ggallus  all identical  ENSGALG00000012663  390DAVSQGASVVTGGKRHSLGKNFF
Trubripes  no homologue    
Drerio  all identical  ENSDARG00000076544  389DHGAVVVRGGKR--LQGSFM
Dmelanogaster  all identical  FBgn0039349  379DARSKKANIILGGQPLPDKGSLFY
Celegans  all identical  F45H10.1  369ICGGKRGEHGTS-Y
Xtropicalis  all identical  ENSXETG00000021961  362NAVSLGAQIEAGGKRSAVGKNFF
protein features
start (aa)end (aa)featuredetails 
423428STRANDmight get lost (downstream of altered splice site)
430433HELIXmight get lost (downstream of altered splice site)
441450STRANDmight get lost (downstream of altered splice site)
452459HELIXmight get lost (downstream of altered splice site)
466471STRANDmight get lost (downstream of altered splice site)
475484HELIXmight get lost (downstream of altered splice site)
487493STRANDmight get lost (downstream of altered splice site)
498498BINDINGSubstrate.might get lost (downstream of altered splice site)
498498MUTAGENS->A: Reduces catalytic activity to less than 15% of wild-type.might get lost (downstream of altered splice site)
508510HELIXmight get lost (downstream of altered splice site)
511513STRANDmight get lost (downstream of altered splice site)
517519TURNmight get lost (downstream of altered splice site)
520524HELIXmight get lost (downstream of altered splice site)
525532STRANDmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1647 / 1647
position (AA) of stopcodon in wt / mu AA sequence 549 / 549
position of stopcodon in wt / mu cDNA 1675 / 1675
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 29 / 29
chromosome 6
strand 1
last intron/exon boundary 1470
theoretical NMD boundary in CDS 1391
length of CDS 1647
coding sequence (CDS) position 1265
cDNA position
(for ins/del: last normal base / first normal base)		 1293
gDNA position
(for ins/del: last normal base / first normal base)		 33198
chromosomal position
(for ins/del: last normal base / first normal base)		 24528277
original gDNA sequence snippet AGGTGCCACCGTTGTGACAGGTGGAAAACGACACCAACTTG
altered gDNA sequence snippet AGGTGCCACCGTTGTGACAGATGGAAAACGACACCAACTTG
original cDNA sequence snippet AGGTGCCACCGTTGTGACAGGTGGAAAACGACACCAACTTG
altered cDNA sequence snippet AGGTGCCACCGTTGTGACAGATGGAAAACGACACCAACTTG
wildtype AA sequence MATCIWLRSC GARRLGSTFP GCRLRPRAGG LVPASGPAPG PAQLRCYAGR LAGLSAALLR
TDSFVGGRWL PAAATFPVQD PASGAALGMV ADCGVREARA AVRAAYEAFC RWREVSAKER
SSLLRKWYNL MIQNKDDLAR IITAESGKPL KEAHGEILYS AFFLEWFSEE ARRVYGDIIH
TPAKDRRALV LKQPIGVAAV ITPWNFPSAM ITRKVGAALA AGCTVVVKPA EDTPFSALAL
AEVNQGFLLD LDPLLLASQA GIPSGVYNVI PCSRKNAKEV GEAICTDPLV SKISFTGSTT
TGKILLHHAA NSVKRVSMEL GGLAPFIVFD SANVDQAVAG AMASKFRNTG QTCVCSNQFL
VQRGIHDAFV KAFAEAMKKN LRVGNGFEEG TTQGPLINEK AVEKVEKQVN DAVSKGATVV
TGGKRHQLGK NFFEPTLLCN VTQDMLCTHE ETFGPLAPVI KFDTEEEAIA IANAADVGLA
GYFYSQDPAQ IWRVAEQLEV GMVGVNEGLI SSVECPFGGV KQSGLGREGS KYGIDEYLEL
KYVCYGGL*
mutated AA sequence MATCIWLRSC GARRLGSTFP GCRLRPRAGG LVPASGPAPG PAQLRCYAGR LAGLSAALLR
TDSFVGGRWL PAAATFPVQD PASGAALGMV ADCGVREARA AVRAAYEAFC RWREVSAKER
SSLLRKWYNL MIQNKDDLAR IITAESGKPL KEAHGEILYS AFFLEWFSEE ARRVYGDIIH
TPAKDRRALV LKQPIGVAAV ITPWNFPSAM ITRKVGAALA AGCTVVVKPA EDTPFSALAL
AEVNQGFLLD LDPLLLASQA GIPSGVYNVI PCSRKNAKEV GEAICTDPLV SKISFTGSTT
TGKILLHHAA NSVKRVSMEL GGLAPFIVFD SANVDQAVAG AMASKFRNTG QTCVCSNQFL
VQRGIHDAFV KAFAEAMKKN LRVGNGFEEG TTQGPLINEK AVEKVEKQVN DAVSKGATVV
TDGKRHQLGK NFFEPTLLCN VTQDMLCTHE ETFGPLAPVI KFDTEEEAIA IANAADVGLA
GYFYSQDPAQ IWRVAEQLEV GMVGVNEGLI SSVECPFGGV KQSGLGREGS KYGIDEYLEL
KYVCYGGL*
speed 0.95 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
back to results table
Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999999999279 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM012724)
  • known disease mutation: rs1359 (pathogenic)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr6:24528277G>AN/A show variant in all transcripts   IGV
HGNC symbol ALDH5A1
Ensembl transcript ID ENST00000546278
Genbank transcript ID N/A
UniProt peptide P51649
alteration type single base exchange
alteration region CDS
DNA changes c.962G>A
cDNA.1029G>A
g.33198G>A
AA changes G321D Score: 94 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 321
frameshift no
known variant Reference ID: rs118203984
databasehomozygous (A/A)heterozygousallele carriers
1000G---
ExAC066

known disease mutation: rs1359 (pathogenic for Succinate-semialdehyde dehydrogenase deficiency) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM012724)

known disease mutation at this position, please check HGMD for details (HGMD ID CM012724)
known disease mutation at this position, please check HGMD for details (HGMD ID CM012724)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)5.8071
5.8071
(flanking)-0.6230.774
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splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor increased33200wt: 0.49 / mu: 0.91wt: CAGGTGGAAAACGAC
mu: CAGATGGAAAACGAC		 GGTG|gaaa
Donor increased33199wt: 0.34 / mu: 0.81wt: ACAGGTGGAAAACGA
mu: ACAGATGGAAAACGA		 AGGT|ggaa
Donor gained331940.59mu: TTGTGACAGATGGAA GTGA|caga
distance from splice site 53
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      321DAVSKGATVVTGGKRHQLGKNFFE
mutated  not conserved    321DAVSKGATVVTDGKRHQLGKNFF
Ptroglodytes  all identical  ENSPTRG00000017776  409DAVSKGATVVTGGKRHQLGKNFF
Mmulatta  all identical  ENSMMUG00000019368  422DAVSKGATIVTGGKRHHLGKNFF
Fcatus  all identical  ENSFCAG00000011094  304VVTGGKRHQLGKNFF
Mmusculus  all identical  ENSMUSG00000035936  397DAVAKGATVVTGGKRHQSGGNFF
Ggallus  all identical  ENSGALG00000012663  390DAVSQGASVVTGGKRHSLGKNFF
Trubripes  no homologue    
Drerio  all identical  ENSDARG00000076544  389DAVDHGAVVVRGGKR--LQGSFM
Dmelanogaster  all identical  FBgn0039349  379DARSKKANIILGGQPLPDKGSLFY
Celegans  all identical  F45H10.1  369DALGKGSELICGGKRGEHGTS-Y
Xtropicalis  all identical  ENSXETG00000021961  362NAVSLGAQIEAGGKRSAVGKNFF
protein features
start (aa)end (aa)featuredetails 
317319STRANDmight get lost (downstream of altered splice site)
321332HELIXlost
334334BINDINGSubstrate.might get lost (downstream of altered splice site)
334334MUTAGENR->A: Reduces catalytic activity to less than 15% of wild-type.might get lost (downstream of altered splice site)
334337HELIXmight get lost (downstream of altered splice site)
340340DISULFIDIn inhibited form.might get lost (downstream of altered splice site)
340340ACT_SITENucleophile (By similarity).might get lost (downstream of altered splice site)
341349STRANDmight get lost (downstream of altered splice site)
342342MUTAGENC->A: Loss of regulation by redox state.might get lost (downstream of altered splice site)
342342DISULFIDIn inhibited form.might get lost (downstream of altered splice site)
350367HELIXmight get lost (downstream of altered splice site)
358358MOD_RESN6-acetyllysine.might get lost (downstream of altered splice site)
373375STRANDmight get lost (downstream of altered splice site)
386400HELIXmight get lost (downstream of altered splice site)
401403TURNmight get lost (downstream of altered splice site)
405408STRANDmight get lost (downstream of altered splice site)
423428STRANDmight get lost (downstream of altered splice site)
430433HELIXmight get lost (downstream of altered splice site)
441450STRANDmight get lost (downstream of altered splice site)
452459HELIXmight get lost (downstream of altered splice site)
466471STRANDmight get lost (downstream of altered splice site)
475484HELIXmight get lost (downstream of altered splice site)
487493STRANDmight get lost (downstream of altered splice site)
498498MUTAGENS->A: Reduces catalytic activity to less than 15% of wild-type.might get lost (downstream of altered splice site)
498498BINDINGSubstrate.might get lost (downstream of altered splice site)
508510HELIXmight get lost (downstream of altered splice site)
511513STRANDmight get lost (downstream of altered splice site)
517519TURNmight get lost (downstream of altered splice site)
520524HELIXmight get lost (downstream of altered splice site)
525532STRANDmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1344 / 1344
position (AA) of stopcodon in wt / mu AA sequence 448 / 448
position of stopcodon in wt / mu cDNA 1411 / 1411
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 68 / 68
chromosome 6
strand 1
last intron/exon boundary 1206
theoretical NMD boundary in CDS 1088
length of CDS 1344
coding sequence (CDS) position 962
cDNA position
(for ins/del: last normal base / first normal base)		 1029
gDNA position
(for ins/del: last normal base / first normal base)		 33198
chromosomal position
(for ins/del: last normal base / first normal base)		 24528277
original gDNA sequence snippet AGGTGCCACCGTTGTGACAGGTGGAAAACGACACCAACTTG
altered gDNA sequence snippet AGGTGCCACCGTTGTGACAGATGGAAAACGACACCAACTTG
original cDNA sequence snippet AGGTGCCACCGTTGTGACAGGTGGAAAACGACACCAACTTG
altered cDNA sequence snippet AGGTGCCACCGTTGTGACAGATGGAAAACGACACCAACTTG
wildtype AA sequence MVADCGVREA RAAVRAAYEA FCRWREVSAK ERSSLLRKWY NLMIQNKDDL ARIITAESGK
PLKEAHGEIL YSAFFLEWFS EEARRVYGDI IHTPAKDRRA LVLKQPIGVA AVITPWNFPS
AMITRKVGAA LAAGCTVVVK PAEDTPFSAL ALAELASQAG IPSGVYNVIP CSRKNAKEVG
EAICTDPLVS KISFTGSTTT GKILLHHAAN SVKRVSMELG GLAPFIVFDS ANVDQAVAGA
MASKFRNTGQ TCVCSNQFLV QRGIHDAFVK AFAEAMKKNL RVGNGFEEGT TQGPLINEKA
VEKVEKQVND AVSKGATVVT GGKRHQLGKN FFEPTLLCNV TQDMLCTHEE TFGPLAPVIK
FDTEEEAIAI ANAADVGLAG YFYSQDPAQI WRVAEQLEVG MVGVNEGLIS SVECPFGGVK
QSGLGREGSK YGIDEYLELK YVCYGGL*
mutated AA sequence MVADCGVREA RAAVRAAYEA FCRWREVSAK ERSSLLRKWY NLMIQNKDDL ARIITAESGK
PLKEAHGEIL YSAFFLEWFS EEARRVYGDI IHTPAKDRRA LVLKQPIGVA AVITPWNFPS
AMITRKVGAA LAAGCTVVVK PAEDTPFSAL ALAELASQAG IPSGVYNVIP CSRKNAKEVG
EAICTDPLVS KISFTGSTTT GKILLHHAAN SVKRVSMELG GLAPFIVFDS ANVDQAVAGA
MASKFRNTGQ TCVCSNQFLV QRGIHDAFVK AFAEAMKKNL RVGNGFEEGT TQGPLINEKA
VEKVEKQVND AVSKGATVVT DGKRHQLGKN FFEPTLLCNV TQDMLCTHEE TFGPLAPVIK
FDTEEEAIAI ANAADVGLAG YFYSQDPAQI WRVAEQLEVG MVGVNEGLIS SVECPFGGVK
QSGLGREGSK YGIDEYLELK YVCYGGL*
speed 0.69 s
All positions are in basepairs (bp) if not explicitly stated differently.
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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Problems