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mutation t@sting

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Prediction

disease causing

Model: without_aae, prob: 1      (explain)
Summary
  • known as potential disease variant: rs92 (probable pathogenic)
  • known disease mutation at this position (HGMD CM993321)
  • protein features (might be) affected
  • splice site changes
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr8:17922010T>AN/A show variant in all transcripts   IGV
HGNC symbol ASAH1
Ensembl transcript ID ENST00000520781
Genbank transcript ID N/A
UniProt peptide Q13510
alteration type single base exchange
alteration region intron
DNA changes g.20485A>T
AA changes N/A
position(s) of altered AA
if AA alteration in CDS
N/A
frameshift N/A
known variant Reference ID: rs137853594
Allele 'A' was neither found in ExAC nor 1000G.
known as potential disease variant: rs92 (probable pathogenic for Farber disease|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM993321)

known disease mutation at this position, please check HGMD for details (HGMD ID CM993321)
known disease mutation at this position, please check HGMD for details (HGMD ID CM993321)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.1910.144
4.5780.998
(flanking)5.5311
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased20492wt: 0.46 / mu: 0.87wt: AATATTTTTTATGAATTATTTACCATTTGTACTTCAATAGT
mu: AATATTTTTTATGTATTATTTACCATTTGTACTTCAATAGT
 attt|ACCA
Acc marginally increased20478wt: 0.4093 / mu: 0.4334 (marginal change - not scored)wt: AGATTATTTCATTCAATATTTTTTATGAATTATTTACCATT
mu: AGATTATTTCATTCAATATTTTTTATGTATTATTTACCATT
 attt|TTTA
Acc increased20496wt: 0.70 / mu: 0.90wt: TTTTTTATGAATTATTTACCATTTGTACTTCAATAGTAGCA
mu: TTTTTTATGTATTATTTACCATTTGTACTTCAATAGTAGCA
 acca|TTTG
Acc marginally increased20485wt: 0.9366 / mu: 0.9401 (marginal change - not scored)wt: TTCATTCAATATTTTTTATGAATTATTTACCATTTGTACTT
mu: TTCATTCAATATTTTTTATGTATTATTTACCATTTGTACTT
 atga|ATTA
Acc increased20489wt: 0.35 / mu: 0.91wt: TTCAATATTTTTTATGAATTATTTACCATTTGTACTTCAAT
mu: TTCAATATTTTTTATGTATTATTTACCATTTGTACTTCAAT
 atta|TTTA
Acc marginally increased20483wt: 0.9218 / mu: 0.9730 (marginal change - not scored)wt: ATTTCATTCAATATTTTTTATGAATTATTTACCATTTGTAC
mu: ATTTCATTCAATATTTTTTATGTATTATTTACCATTTGTAC
 ttat|GAAT
Acc increased20481wt: 0.41 / mu: 0.45wt: TTATTTCATTCAATATTTTTTATGAATTATTTACCATTTGT
mu: TTATTTCATTCAATATTTTTTATGTATTATTTACCATTTGT
 tttt|ATGA
Acc marginally increased20476wt: 0.5256 / mu: 0.5360 (marginal change - not scored)wt: AGAGATTATTTCATTCAATATTTTTTATGAATTATTTACCA
mu: AGAGATTATTTCATTCAATATTTTTTATGTATTATTTACCA
 atat|TTTT
Acc gained204870.42mu: CATTCAATATTTTTTATGTATTATTTACCATTTGTACTTCA gtat|TATT
Acc gained204900.69mu: TCAATATTTTTTATGTATTATTTACCATTTGTACTTCAATA ttat|TTAC
Acc gained204950.43mu: ATTTTTTATGTATTATTTACCATTTGTACTTCAATAGTAGC tacc|ATTT
Acc gained204940.44mu: TATTTTTTATGTATTATTTACCATTTGTACTTCAATAGTAG ttac|CATT
Donor gained204780.38mu: ATATTTTTTATGTAT ATTT|ttta
distance from splice site 1271
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
N/A
protein features
start (aa)end (aa)featuredetails 
155155CONFLICTL -> P (in Ref. 4; AAQ75550).might get lost (downstream of altered splice site)
173173CARBOHYDN-linked (GlcNAc...) (Potential).might get lost (downstream of altered splice site)
195195CARBOHYDN-linked (GlcNAc...) (Potential).might get lost (downstream of altered splice site)
233233CONFLICTY -> N (in Ref. 4; AAQ75550).might get lost (downstream of altered splice site)
259259CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
286286CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
342342CARBOHYDN-linked (GlcNAc...) (Potential).might get lost (downstream of altered splice site)
348348CARBOHYDN-linked (GlcNAc...) (Potential).might get lost (downstream of altered splice site)
364364CONFLICTL -> P (in Ref. 4; AAQ75550).might get lost (downstream of altered splice site)
length of protein N/A
AA sequence altered N/A
position of stopcodon in wt / mu CDS N/A
position (AA) of stopcodon in wt / mu AA sequence N/A
position of stopcodon in wt / mu cDNA N/A
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 313 / 313
chromosome 8
strand -1
last intron/exon boundary 1336
theoretical NMD boundary in CDS 973
length of CDS 1113
coding sequence (CDS) position N/A
cDNA position
(for ins/del: last normal base / first normal base)
N/A
gDNA position
(for ins/del: last normal base / first normal base)
20485
chromosomal position
(for ins/del: last normal base / first normal base)
17922010
original gDNA sequence snippet TTCATTCAATATTTTTTATGAATTATTTACCATTTGTACTT
altered gDNA sequence snippet TTCATTCAATATTTTTTATGTATTATTTACCATTTGTACTT
original cDNA sequence snippet N/A
altered cDNA sequence snippet N/A
wildtype AA sequence MPGRSCVALV LLAAAVSCAV AQHAPPWTED CRKSTYPPSG PTYRGAVPWY TINLDLPPYK
RWHELMLDKA PVLKVIVNSL KNMINTFVPS GKIMQVVDEK LPGLLGNFPG PFEEEMKGIA
AVTDIPLGHL IHGRNMDFGV FLGWNINNDT WVITEQLKPL TVNLDFQRNN KTVFKASSFA
GYVGMLTGFK PGLFSLTLNE RFSINGGYLG ILEWILGKKD VMWIGFLTRT VLENSTSYEE
AKNLLTKTKI LAPAYFILGG NQSGEGCVIT RDRKESLDVY ELDAKQGRWY VVQTNYDRWK
HPFFLDDRRT PAKMCLNRTS QENISFETMY DVLSTKPVLN KLTVYTTLID VTKGQFETYL
RDCPDPCIGW *
mutated AA sequence N/A
speed 0.64 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