Variant #0001874003 (NC_000020.10:g.62493865G>A, NM_080622.3:c.972G>A (ABHD16B))

Chromosome 20
DNA change (genomic) (Relative to hg19 / GRCh37) g.62493865G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD16B_000034
Frequency 89/12928
Freq. EA 4/8560
Freq. AA 85/4368
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 16:46:43 +02:00 (CEST)
Date last edited 2018-09-30 11:55:53 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABHD16B NM_080622.3 ?/? c.972G>A r.(=) p.(=)