Yum, tasty mutations...

mutation t@sting

documentation

Prediction

disease causing

Model: simple_aae, prob: 0.999987538582957 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM994594)
  • known disease mutation: rs2612 (pathogenic)
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr17:3397701A>GN/A show variant in all transcripts   IGV
HGNC symbol ASPA
Ensembl transcript ID ENST00000263080
Genbank transcript ID NM_000049
UniProt peptide P45381
alteration type single base exchange
alteration region CDS
DNA changes c.692A>G
cDNA.850A>G
g.22034A>G
AA changes Y231C Score: 194 explain score(s)
position(s) of altered AA
if AA alteration in CDS
231
frameshift no
known variant Reference ID: rs104894550
databasehomozygous (G/G)heterozygousallele carriers
1000G---
ExAC011

known disease mutation: rs2612 (pathogenic for Spongy degeneration of central nervous system) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM994594)

known disease mutation at this position, please check HGMD for details (HGMD ID CM994594)
known disease mutation at this position, please check HGMD for details (HGMD ID CM994594)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)4.3741
1.2951
(flanking)0.8831
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites no abrogation of potential splice sites
distance from splice site 53
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      231IEVYKIIEKVDYPRDENGEIAAII
mutated  not conserved    231IEVYKIIEKVDCPRDENGEIA
Ptroglodytes  all identical  ENSPTRG00000008568  231IEVYKIIEKVDYPRDENGEIA
Mmulatta  all identical  ENSMMUG00000030388  231IEVYKIIEKVDYPRDENGEIA
Fcatus  all identical  ENSFCAG00000007919  231IEVYKIMEKIDYPRNEN
Mmusculus  all identical  ENSMUSG00000020774  230IDVYKIMEKVDYPRNESGDMA
Ggallus  all identical  ENSGALG00000004669  232IEVYKITEKVDYPRNKNDEV
Trubripes  no homologue    
Drerio  all identical  ENSDARG00000005154  233VNVFRVQERMDYPRDTNGNITAM
Dmelanogaster  no homologue    
Celegans  no homologue    
Xtropicalis  all identical  ENSXETG00000005789  230LEVFKVLDNVAYPRNANGDCTAI
protein features no protein features affected
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 942 / 942
position (AA) of stopcodon in wt / mu AA sequence 314 / 314
position of stopcodon in wt / mu cDNA 1100 / 1100
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 159 / 159
chromosome 17
strand 1
last intron/exon boundary 903
theoretical NMD boundary in CDS 694
length of CDS 942
coding sequence (CDS) position 692
cDNA position
(for ins/del: last normal base / first normal base)
850
gDNA position
(for ins/del: last normal base / first normal base)
22034
chromosomal position
(for ins/del: last normal base / first normal base)
3397701
original gDNA sequence snippet AATTATAGAGAAAGTTGATTACCCCCGGGATGAAAATGGAG
altered gDNA sequence snippet AATTATAGAGAAAGTTGATTGCCCCCGGGATGAAAATGGAG
original cDNA sequence snippet AATTATAGAGAAAGTTGATTACCCCCGGGATGAAAATGGAG
altered cDNA sequence snippet AATTATAGAGAAAGTTGATTGCCCCCGGGATGAAAATGGAG
wildtype AA sequence MTSCHIAEEH IQKVAIFGGT HGNELTGVFL VKHWLENGAE IQRTGLEVKP FITNPRAVKK
CTRYIDCDLN RIFDLENLGK KMSEDLPYEV RRAQEINHLF GPKDSEDSYD IIFDLHNTTS
NMGCTLILED SRNNFLIQMF HYIKTSLAPL PCYVYLIEHP SLKYATTRSI AKYPVGIEVG
PQPQGVLRAD ILDQMRKMIK HALDFIHHFN EGKEFPPCAI EVYKIIEKVD YPRDENGEIA
AIIHPNLQDQ DWKPLHPGDP MFLTLDGKTI PLGGDCTVYP VFVNEAAYYE KKEAFAKTTK
LTLNAKSIRC CLH*
mutated AA sequence MTSCHIAEEH IQKVAIFGGT HGNELTGVFL VKHWLENGAE IQRTGLEVKP FITNPRAVKK
CTRYIDCDLN RIFDLENLGK KMSEDLPYEV RRAQEINHLF GPKDSEDSYD IIFDLHNTTS
NMGCTLILED SRNNFLIQMF HYIKTSLAPL PCYVYLIEHP SLKYATTRSI AKYPVGIEVG
PQPQGVLRAD ILDQMRKMIK HALDFIHHFN EGKEFPPCAI EVYKIIEKVD CPRDENGEIA
AIIHPNLQDQ DWKPLHPGDP MFLTLDGKTI PLGGDCTVYP VFVNEAAYYE KKEAFAKTTK
LTLNAKSIRC CLH*
speed 1.31 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