Variant #0001873987 (NC_000020.10:g.62493384C>T, NM_080622.3:c.491C>T (ABHD16B))

Chromosome 20
DNA change (genomic) (Relative to hg19 / GRCh37) g.62493384C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD16B_000018
Frequency 101/12990
Freq. EA 17/8596
Freq. AA 84/4394
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 11:54:05 +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.491C>T r.(?) p.(Pro164Leu)