Yum, tasty mutations...

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 CM000499)
  • known disease mutation: rs5422 (pathogenic)
  • protein features (might be) affected
  • splice site changes
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr19:39200947T>CN/A show variant in all transcripts   IGV
HGNC symbol ACTN4
Ensembl transcript ID ENST00000424234
Genbank transcript ID N/A
UniProt peptide O43707
alteration type single base exchange
alteration region intron
DNA changes g.62659T>C
AA changes N/A
position(s) of altered AA
if AA alteration in CDS
N/A
frameshift N/A
known variant Reference ID: rs121908417
Allele 'C' was neither found in ExAC nor 1000G.
known disease mutation: rs5422 (pathogenic for Focal segmental glomerulosclerosis 1) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM000499)

known disease mutation at this position, please check HGMD for details (HGMD ID CM000499)
known disease mutation at this position, please check HGMD for details (HGMD ID CM000499)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H3K4me1, Histone, Histone 3 Lysine 4 Mono-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)2.4381
4.3921
(flanking)5.3031
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor increased62657wt: 0.24 / mu: 0.29wt: CTATGTGTCCAGCTT
mu: CTATGTGCCCAGCTT
 ATGT|gtcc
Donor increased62662wt: 0.28 / mu: 0.36wt: TGTCCAGCTTCTACC
mu: TGCCCAGCTTCTACC
 TCCA|gctt
Donor marginally increased62650wt: 0.9714 / mu: 0.9786 (marginal change - not scored)wt: TAATGACCTATGTGT
mu: TAATGACCTATGTGC
 ATGA|ccta
distance from splice site 7944
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
N/A
protein features
start (aa)end (aa)featuredetails 
1269DOMAINActin-binding.might get lost (downstream of altered splice site)
50154DOMAINCH 1.might get lost (downstream of altered splice site)
8292HELIXmight get lost (downstream of altered splice site)
105120HELIXmight get lost (downstream of altered splice site)
114114MOD_RESN6-acetyllysine.might get lost (downstream of altered splice site)
121123TURNmight get lost (downstream of altered splice site)
131135HELIXmight get lost (downstream of altered splice site)
139153HELIXmight get lost (downstream of altered splice site)
154157TURNmight get lost (downstream of altered splice site)
163269DOMAINCH 2.might get lost (downstream of altered splice site)
164164CONFLICTS -> L (in Ref. 4; AL047603/AU118403).might get lost (downstream of altered splice site)
165177HELIXmight get lost (downstream of altered splice site)
177192REGIONPolyphosphoinositide (PIP2)-binding (Potential).might get lost (downstream of altered splice site)
187189STRANDmight get lost (downstream of altered splice site)
190192HELIXmight get lost (downstream of altered splice site)
196205HELIXmight get lost (downstream of altered splice site)
207209HELIXmight get lost (downstream of altered splice site)
212214HELIXmight get lost (downstream of altered splice site)
214214MOD_RESN6-acetyllysine.might get lost (downstream of altered splice site)
220234HELIXmight get lost (downstream of altered splice site)
243248HELIXmight get lost (downstream of altered splice site)
249251STRANDmight get lost (downstream of altered splice site)
254267HELIXmight get lost (downstream of altered splice site)
265265MOD_RESPhosphotyrosine.might get lost (downstream of altered splice site)
276276CONFLICTT -> TET (in Ref. 3; AAC17470).might get lost (downstream of altered splice site)
292294CONFLICTEHL -> CSTS (in Ref. 3; AAC17470).might get lost (downstream of altered splice site)
293403REPEATSpectrin 1.might get lost (downstream of altered splice site)
359360CONFLICTTL -> SV (in Ref. 3; AAC17470).might get lost (downstream of altered splice site)
378378CROSSLNKGlycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in ubiquitin).might get lost (downstream of altered splice site)
413518REPEATSpectrin 2.might get lost (downstream of altered splice site)
417417MOD_RESN6-acetyllysine.might get lost (downstream of altered splice site)
476476CONFLICTI -> S (in Ref. 3; AAC17470).might get lost (downstream of altered splice site)
519552HELIXmight get lost (downstream of altered splice site)
526526CONFLICTI -> II (in Ref. 3; AAC17470).might get lost (downstream of altered splice site)
528639REPEATSpectrin 3.might get lost (downstream of altered splice site)
536536CONFLICTR -> P (in Ref. 3; AAC17470).might get lost (downstream of altered splice site)
560600HELIXmight get lost (downstream of altered splice site)
592592MOD_RESN6-acetyllysine.might get lost (downstream of altered splice site)
606608STRANDmight get lost (downstream of altered splice site)
616641HELIXmight get lost (downstream of altered splice site)
625625MOD_RESN6-acetyllysine.might get lost (downstream of altered splice site)
645645CONFLICTQ -> QQ (in Ref. 3; AAC17470).might get lost (downstream of altered splice site)
649752REPEATSpectrin 4.might get lost (downstream of altered splice site)
673674CONFLICTGR -> A (in Ref. 3; AAC17470).might get lost (downstream of altered splice site)
736756HELIXmight get lost (downstream of altered splice site)
765800DOMAINEF-hand 1.might get lost (downstream of altered splice site)
778789CA_BIND1 (Potential).might get lost (downstream of altered splice site)
806841DOMAINEF-hand 2.might get lost (downstream of altered splice site)
819830CA_BIND2 (Potential).might get lost (downstream of altered splice site)
850850CONFLICTA -> T (in Ref. 3; AAC17470).might get lost (downstream of altered splice site)
891893CONFLICTAVP -> GVR (in Ref. 3; AAC17470).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 60 / 60
chromosome 19
strand 1
last intron/exon boundary 1467
theoretical NMD boundary in CDS 1357
length of CDS 1566
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)
62659
chromosomal position
(for ins/del: last normal base / first normal base)
39200947
original gDNA sequence snippet AGGCCATAATGACCTATGTGTCCAGCTTCTACCATGCCTTT
altered gDNA sequence snippet AGGCCATAATGACCTATGTGCCCAGCTTCTACCATGCCTTT
original cDNA sequence snippet N/A
altered cDNA sequence snippet N/A
wildtype AA sequence MVDYHAANQS YQYGPSSAGN GAGGGGSMGD YMAQEDDWDR DLLLDPAWEK QQRKTFTAWC
NSHLRKAGTQ IENIDEDFRD GLKLMLLLEV HELDYYDSHN VNTRCQKICD QWDALGSLTH
SRREALEKTE KQLEAIDQLH LEYAKRAAPF NNWMESAMED LQDMFIVHTI EEIEGLISAH
DQFKSTLPDA DREREAILAI HKEAQRIAES NHIKLSGSNP YTTVTPQIIN SKWEKVQQLV
PKRDHALLEE QSKQQSNEHL RRQFASQANV VGPWIQTKME EIGRISIEMN GTLEDQLSHL
KQYERSIVDY KPNLDLLEQQ HQLIQEALIF DNKHTNYTME HIRVGWEQLL TTIARTINEV
ENQILTRDAK GISQEQMQEF RASFNHFDKD HGGALGPEEF KACLISLGYD VENDRQGEAE
FNRIMSLVDP NHSGLVTFQA FIDFMSRETT DTDTADQVIA SFKVLAGDKN FITAEELRRE
LPPDQAEYCI ARMAPYQGPD AVPGALDYKS FSTALYGESD L*
mutated AA sequence N/A
speed 1.05 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