Variant #0001675729 (NC_000018.9:g.60795996C>A, NC_000018.9(NM_000633.2):c.586-4G>T (BCL2))

Chromosome 18
DNA change (genomic) (Relative to hg19 / GRCh37) g.60795996C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL2_000009
Frequency 2/13006
Freq. EA 0/8600
Freq. AA 2/4406
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 21:17:11 +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.586-4G>T r.spl? p.?