Variant #0001915321 (NC_000022.10:g.29107873G>A, NC_000022.10(NM_001005735.1):c.921+24C>T (CHEK2))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.29107873G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CHEK2_000048
Frequency 3/13002
Freq. EA 3/8598
Freq. AA 0/4404
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 07:42:00 +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.921+24C>T r.(=) p.(=)