Variant #0001915288 (NC_000022.10:g.29091178C>A, NM_001005735.1:c.1441G>T (CHEK2))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.29091178C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CHEK2_000015
Frequency 4/13006
Freq. EA 3/8600
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 11:56:24 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CHEK2 NM_001005735.1 ?/? c.1441G>T r.(?) p.(Asp481Tyr)