Variant #0000420298 (NC_000001.10:g.45797835T>G, NC_000001.10(NM_001128425.1):c.933+3A>C (MUTYH))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.45797835T>G
DNA change (hg38) g.45332163T>G
Published as 16616356_933_3_RT_PCR
ISCN -
DB-ID MUTYH_000097 See all 42 reported entries
Variant remarks cDNA analysis; Skipping exon 10
Reference PubMed: Kanter-Smoler 2006
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 7.0E-5 View details
Owner Astrid Out
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Astrid Out
Date created 2010-07-26 21:40:56 +02:00 (CEST)
Date last edited 2020-07-14 21:57:48 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
MUTYH NM_001128425.1 +/. 10i c.933+3A>C r.spl? p.Gly264Trpfs*7 -


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