Variant #0001915309 (NC_000022.10:g.29095813G>A, NC_000022.10(NM_001005735.1):c.1137+13C>T (CHEK2))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.29095813G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CHEK2_000036
Frequency 2/13006
Freq. EA 2/8600
Freq. AA 0/4406
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 2013-05-06 07:41:55 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CHEK2 NM_001005735.1 ?/? c.1137+13C>T r.(=) p.(=)