Yum, tasty mutations...

mutation t@sting

documentation

Prediction

disease causing

Model: simple_aae, prob: 0.000359704251868706 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM023571)
  • known disease mutation: rs7760 (pathogenic)
  • protein features (might be) affected
  • splice site changes
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr2:202141631C>TN/A show variant in all transcripts   IGV
HGNC symbol CASP8
Ensembl transcript ID ENST00000392259
Genbank transcript ID N/A
UniProt peptide Q14790
alteration type single base exchange
alteration region CDS
DNA changes c.677C>T
cDNA.912C>T
g.43466C>T
AA changes T226M Score: 81 explain score(s)
position(s) of altered AA
if AA alteration in CDS
226
frameshift no
known variant Reference ID: rs17860424
databasehomozygous (T/T)heterozygousallele carriers
1000G---
ExAC022

known disease mutation: rs7760 (pathogenic for Autoimmune lymphoproliferative syndrome type 2B) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM023571)

known disease mutation at this position, please check HGMD for details (HGMD ID CM023571)
known disease mutation at this position, please check HGMD for details (HGMD ID CM023571)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.2290.945
0.6540.941
(flanking)2.8340.936
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor increased43462wt: 0.23 / mu: 0.57wt: GCAAAAGCACGGGAG
mu: GCAAAAGCATGGGAG
 AAAA|gcac
Donor marginally increased43469wt: 0.9913 / mu: 0.9916 (marginal change - not scored)wt: CACGGGAGAAAGTGC
mu: CATGGGAGAAAGTGC
 CGGG|agaa
Donor increased43470wt: 0.34 / mu: 0.38wt: ACGGGAGAAAGTGCC
mu: ATGGGAGAAAGTGCC
 GGGA|gaaa
distance from splice site 61
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      226SDHQQSQFCKSTGESAQTSQH*
mutated  not conserved    226SDHQQSQFCKSMGESAQTSQH
Ptroglodytes  no alignment  ENSPTRG00000012801  n/a
Mmulatta  no alignment  ENSMMUG00000031296  n/a
Fcatus  no homologue    
Mmusculus  no alignment  ENSMUSG00000026029  n/a
Ggallus  no alignment  ENSGALG00000008355  n/a
Trubripes  no alignment  ENSTRUG00000009617  n/a
Drerio  no homologue    
Dmelanogaster  no alignment  FBgn0019972  n/a
Celegans  no homologue    
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
230232STRANDmight get lost (downstream of altered splice site)
235240STRANDmight get lost (downstream of altered splice site)
246249HELIXmight get lost (downstream of altered splice site)
252254HELIXmight get lost (downstream of altered splice site)
255257STRANDmight get lost (downstream of altered splice site)
263276HELIXmight get lost (downstream of altered splice site)
280286STRANDmight get lost (downstream of altered splice site)
289301HELIXmight get lost (downstream of altered splice site)
294294CONFLICTE -> D (in Ref. 5; AAD24962).might get lost (downstream of altered splice site)
310316STRANDmight get lost (downstream of altered splice site)
317317ACT_SITEmight get lost (downstream of altered splice site)
322324STRANDmight get lost (downstream of altered splice site)
326328STRANDmight get lost (downstream of altered splice site)
330332STRANDmight get lost (downstream of altered splice site)
331331CONFLICTA -> P (in Ref. 2; AAC50602 and 5; AAD24962).might get lost (downstream of altered splice site)
333337HELIXmight get lost (downstream of altered splice site)
334334MOD_RESPhosphotyrosine.might get lost (downstream of altered splice site)
338340HELIXmight get lost (downstream of altered splice site)
342344TURNmight get lost (downstream of altered splice site)
343344CONFLICTLK -> FG (in Ref. 8; AAL87631).might get lost (downstream of altered splice site)
346348HELIXmight get lost (downstream of altered splice site)
353359STRANDmight get lost (downstream of altered splice site)
360360ACT_SITEmight get lost (downstream of altered splice site)
362364STRANDmight get lost (downstream of altered splice site)
375384PROPEP /FTId=PRO_0000004630.might get lost (downstream of altered splice site)
377379STRANDmight get lost (downstream of altered splice site)
387387MUTAGENS->A: Impaired CDK1-mediated phosphorylation and enhanced apoptosis.might get lost (downstream of altered splice site)
387387MOD_RESPhosphoserine; by CDK1.might get lost (downstream of altered splice site)
395405STRANDmight get lost (downstream of altered splice site)
412414STRANDmight get lost (downstream of altered splice site)
415417TURNmight get lost (downstream of altered splice site)
420432HELIXmight get lost (downstream of altered splice site)
433435HELIXmight get lost (downstream of altered splice site)
439451HELIXmight get lost (downstream of altered splice site)
456459TURNmight get lost (downstream of altered splice site)
465468STRANDmight get lost (downstream of altered splice site)
471473STRANDmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 708 / 708
position (AA) of stopcodon in wt / mu AA sequence 236 / 236
position of stopcodon in wt / mu cDNA 943 / 943
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 236 / 236
chromosome 2
strand 1
last intron/exon boundary 1475
theoretical NMD boundary in CDS 1189
length of CDS 708
coding sequence (CDS) position 677
cDNA position
(for ins/del: last normal base / first normal base)
912
gDNA position
(for ins/del: last normal base / first normal base)
43466
chromosomal position
(for ins/del: last normal base / first normal base)
202141631
original gDNA sequence snippet ATCACAATTTTGCAAAAGCACGGGAGAAAGTGCCCAAACTT
altered gDNA sequence snippet ATCACAATTTTGCAAAAGCATGGGAGAAAGTGCCCAAACTT
original cDNA sequence snippet ATCACAATTTTGCAAAAGCACGGGAGAAAGTGCCCAAACTT
altered cDNA sequence snippet ATCACAATTTTGCAAAAGCATGGGAGAAAGTGCCCAAACTT
wildtype AA sequence MDFSRNLYDI GEQLDSEDLA SLKFLSLDYI PQRKQEPIKD ALMLFQRLQE KRMLEESNLS
FLKELLFRIN RLDLLITYLN TRKEEMEREL QTPGRAQISA YRVMLYQISE EVSRSELRSF
KFLLQEEISK CKLDDDMNLL DIFIEMEKRV ILGEGKLDIL KRVCAQINKS LLKIINDYEE
FSKERSSSLE GSPDEFSNDF GQSLPNEKQT SGILSDHQQS QFCKSTGESA QTSQH*
mutated AA sequence MDFSRNLYDI GEQLDSEDLA SLKFLSLDYI PQRKQEPIKD ALMLFQRLQE KRMLEESNLS
FLKELLFRIN RLDLLITYLN TRKEEMEREL QTPGRAQISA YRVMLYQISE EVSRSELRSF
KFLLQEEISK CKLDDDMNLL DIFIEMEKRV ILGEGKLDIL KRVCAQINKS LLKIINDYEE
FSKERSSSLE GSPDEFSNDF GQSLPNEKQT SGILSDHQQS QFCKSMGESA QTSQH*
speed 1.27 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