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mutation t@sting

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Prediction

disease causing

Model: without_aae, prob: 1 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • known disease mutation at this position (HGMD CM992118)
  • known disease mutation: rs18279 (pathogenic)
  • protein features (might be) affected
  • splice site changes
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr1:229568470A>GN/A show variant in all transcripts   IGV
HGNC symbol ACTA1
Ensembl transcript ID ENST00000366682
Genbank transcript ID N/A
UniProt peptide P68133
alteration type single base exchange
alteration region intron
DNA changes g.1376T>C
AA changes N/A
position(s) of altered AA
if AA alteration in CDS
N/A
frameshift N/A
known variant Reference ID: rs121909519
Allele 'G' was neither found in ExAC nor 1000G.
known disease mutation: rs18279 (pathogenic for Nemaline myopathy 3) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM992118)

known disease mutation at this position, please check HGMD for details (HGMD ID CM992118)
known disease mutation at this position, please check HGMD for details (HGMD ID CM992118)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)-0.8210.771
4.6591
(flanking)5.641
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased1373wt: 0.46 / mu: 0.62wt: GCACCACACCTTCTACAACGAGCTTCGCGTGGCTCCCGAGG
mu: GCACCACACCTTCTACAACGAGCCTCGCGTGGCTCCCGAGG
 acga|GCTT
Acc increased1370wt: 0.24 / mu: 0.34wt: CTGGCACCACACCTTCTACAACGAGCTTCGCGTGGCTCCCG
mu: CTGGCACCACACCTTCTACAACGAGCCTCGCGTGGCTCCCG
 acaa|CGAG
Donor marginally increased1373wt: 0.8504 / mu: 0.9218 (marginal change - not scored)wt: CAACGAGCTTCGCGT
mu: CAACGAGCCTCGCGT
 ACGA|gctt
Donor increased1368wt: 0.38 / mu: 0.47wt: TTCTACAACGAGCTT
mu: TTCTACAACGAGCCT
 CTAC|aacg
distance from splice site 48
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
N/A
protein features
start (aa)end (aa)featuredetails 
8193HELIXmight get lost (downstream of altered splice site)
9393MOD_RESPhosphotyrosine.might get lost (downstream of altered splice site)
100102HELIXmight get lost (downstream of altered splice site)
105109STRANDmight get lost (downstream of altered splice site)
115127HELIXmight get lost (downstream of altered splice site)
132138STRANDmight get lost (downstream of altered splice site)
139146HELIXmight get lost (downstream of altered splice site)
154157STRANDmight get lost (downstream of altered splice site)
162165STRANDmight get lost (downstream of altered splice site)
174176HELIXmight get lost (downstream of altered splice site)
178180STRANDmight get lost (downstream of altered splice site)
186197HELIXmight get lost (downstream of altered splice site)
193193MOD_RESN6-acetyllysine.might get lost (downstream of altered splice site)
205218HELIXmight get lost (downstream of altered splice site)
225234HELIXmight get lost (downstream of altered splice site)
240243STRANDmight get lost (downstream of altered splice site)
242242MOD_RESPhosphotyrosine (By similarity).might get lost (downstream of altered splice site)
249252STRANDmight get lost (downstream of altered splice site)
255264HELIXmight get lost (downstream of altered splice site)
266268HELIXmight get lost (downstream of altered splice site)
277284HELIXmight get lost (downstream of altered splice site)
289291TURNmight get lost (downstream of altered splice site)
292297HELIXmight get lost (downstream of altered splice site)
299302STRANDmight get lost (downstream of altered splice site)
312320HELIXmight get lost (downstream of altered splice site)
328328MOD_RESN6-acetyllysine.might get lost (downstream of altered splice site)
330330MOD_RESN6-acetyllysine.might get lost (downstream of altered splice site)
335338TURNmight get lost (downstream of altered splice site)
340342TURNmight get lost (downstream of altered splice site)
347350HELIXmight get lost (downstream of altered splice site)
354357HELIXmight get lost (downstream of altered splice site)
358360STRANDmight get lost (downstream of altered splice site)
361366HELIXmight get lost (downstream of altered splice site)
371375HELIXmight 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 104 / 104
chromosome 1
strand -1
last intron/exon boundary 989
theoretical NMD boundary in CDS 835
length of CDS 1029
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)
1376
chromosomal position
(for ins/del: last normal base / first normal base)
229568470
original gDNA sequence snippet CCACACCTTCTACAACGAGCTTCGCGTGGCTCCCGAGGAGC
altered gDNA sequence snippet CCACACCTTCTACAACGAGCCTCGCGTGGCTCCCGAGGAGC
original cDNA sequence snippet N/A
altered cDNA sequence snippet N/A
wildtype AA sequence MCDEDETTAL VCDNGSGLVK AGFAGDDAPR AVFPSIVGRP RHQGVMVGMG QKDSYVGDEA
QSKRGILTLK YPIEHGIITK ANREKMTQIM FETFNVPAMY VAIQAVLSLY ASGRTTGIVL
DSGDGVTHNV PIYEGYALPH AIMRLDLAGR DLTDYLMKIL TERGYSFVTT AEREIVRDIK
EKLCYVALDF ENEMATAASS SSLEKSYELP DGQVITIGNE RFRCPETLFQ PSFIGMESAG
IHETTYNSIM KCDIDIRKDL YANNVMSGGT TMYPGIADRM QKEITALAPS TMKIKIIAPP
ERKYSVWIGG SILASLSTFQ QMWITKQEYD EAGPSIVHRK CF*
mutated AA sequence N/A
speed 0.78 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