Variant #0001837659 (NC_000020.10:g.25289097C>A, NM_015600.4:c.783G>T (ABHD12))

Chromosome 20
DNA change (genomic) (Relative to hg19 / GRCh37) g.25289097C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD12_000046
Frequency 1/13004
Freq. EA 1/8600
Freq. AA 0/4404
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 2018-08-23 09:15:54 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABHD12 NM_015600.4 ?/? c.783G>T r.(?) p.(Glu261Asp)