Variant #0000382795 (NC_000003.11:g.52005463G>T, NC_000003.11(NM_032750.2):c.211+13C>A (ABHD14B))

Chromosome 3
DNA change (genomic) (Relative to hg19 / GRCh37) g.52005463G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD14B_000021
Frequency 6/13000
Freq. EA 6/8600
Freq. AA 0/4400
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 16:23:53 +02:00 (CEST)
Date last edited 2018-09-30 11:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABHD14B NM_032750.2 ?/? c.211+13C>A r.(=) p.(=)