Variant #0001675743 (NC_000018.9:g.60985879T>C, NM_000633.2:c.21A>G (BCL2))

Chromosome 18
DNA change (genomic) (Relative to hg19 / GRCh37) g.60985879T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL2_000023
Frequency 3739/12044
Freq. EA 3402/8130
Freq. AA 337/3914
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 16:45:07 +02:00 (CEST)
Date last edited 2013-05-05 21:17:16 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BCL2 NM_000633.2 ?/? c.21A>G r.(=) p.(=)