Variant #0001675733 (NC_000018.9:g.60985299C>T, NC_000018.9(NM_000633.2):c.585+16G>A (BCL2))

Chromosome 18
DNA change (genomic) (Relative to hg19 / GRCh37) g.60985299C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL2_000013
Frequency 1/13006
Freq. EA 1/8600
Freq. AA 0/4406
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.585+16G>A r.(=) p.(=)