Variant #0001323908 (NC_000014.8:g.51352331G>C, NC_000014.8(NM_001206673.1):c.487-1G>C (ABHD12B))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.51352331G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD12B_000023
Frequency 2/13006
Freq. EA 2/8600
Freq. AA 0/4406
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 03:42:18 +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.487-1G>C r.spl? p.?