Variant #0001915347 (NC_000022.10:g.29121072_29121074del, NM_001005735.1:c.612_614del (CHEK2))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.29121072_29121074del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CHEK2_000074
Frequency 1/12516
Freq. EA 0/8254
Freq. AA 1/4262
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 2016-12-02 21:10:48 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CHEK2 NM_001005735.1 ?/? c.612_614del r.(?) p.(Glu204del)