Variant #0001794504 (NC_000019.9:g.50172127C>G, NM_001040668.1:c.519C>G (BCL2L12))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.50172127C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL2L12_000036
Frequency 3/13006
Freq. EA 0/8600
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 16:45:39 +02:00 (CEST)
Date last edited 2013-05-06 02:23:15 +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.519C>G r.(?) p.(Phe173Leu)