Variant #0001323909 (NC_000014.8:g.51352345G>A, NM_001206673.1:c.500G>A (ABHD12B))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.51352345G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD12B_000024
Frequency 568/13006
Freq. EA 502/8600
Freq. AA 66/4406
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 16:41:19 +02:00 (CEST)
Date last edited 2018-08-23 09:42:27 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABHD12B NM_001206673.1 ?/? c.500G>A r.(?) p.(Gly167Asp)