Variant #0001675736 (NC_000018.9:g.60985441G>A, NM_000633.2:c.459C>T (BCL2))

Chromosome 18
DNA change (genomic) (Relative to hg19 / GRCh37) g.60985441G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL2_000016
Frequency 14/13006
Freq. EA 11/8600
Freq. AA 3/4406
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 16:45:07 +02:00 (CEST)
Date last edited 2013-05-05 21:17:15 +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.459C>T r.(=) p.(=)