Variant #0001915362 (NC_000022.10:g.29121360A>T, NC_000022.10(NM_001005735.1):c.449-5T>A (CHEK2))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.29121360A>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CHEK2_000089
Frequency 5/13006
Freq. EA 4/8600
Freq. AA 1/4406
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:50:05 +02:00 (CEST)
Date last edited 2018-09-30 11:51:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CHEK2 NM_001005735.1 ?/? c.449-5T>A r.spl? p.?