Variant #0001915335 (NC_000022.10:g.29120926del, NC_000022.10(NM_001005735.1):c.721+39del (CHEK2))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.29120926del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CHEK2_000062
Frequency 91/12518
Freq. EA 41/8254
Freq. AA 50/4264
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 07:42:01 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CHEK2 NM_001005735.1 ?/? c.721+39del r.(=) p.(=)