Variant #0001323967 (NC_000014.8:g.51371150C>T, NM_001206673.1:c.*66C>T (ABHD12B))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.51371150C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD12B_000082
Frequency 774/4566
Freq. EA 582/3182
Freq. AA 192/1384
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 10:29:20 +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.*66C>T r.(=) p.(=)