Variant #0001675742 (NC_000018.9:g.60985773C>T, NM_000633.2:c.127G>A (BCL2))

Chromosome 18
DNA change (genomic) (Relative to hg19 / GRCh37) g.60985773C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL2_000022
Frequency 8/11808
Freq. EA 2/8060
Freq. AA 6/3748
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.127G>A r.(?) p.(Ala43Thr)