Variant #0001794520 (NC_000019.9:g.50173731G>T, NM_001040668.1:c.937G>T (BCL2L12))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.50173731G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL2L12_000052
Frequency 4/11662
Freq. EA 0/7760
Freq. AA 4/3902
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 16:45:39 +02:00 (CEST)
Date last edited 2013-05-06 02:23:17 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BCL2L12 NM_001040668.1 ?/? c.937G>T r.(?) p.(Ala313Ser)