Variant #0001323955 (NC_000014.8:g.51370192del, NC_000014.8(NM_001206673.1):c.942+7del (ABHD12B))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.51370192del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD12B_000070
Frequency 1/12518
Freq. EA 0/8254
Freq. AA 1/4264
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 04:34:23 +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.942+7del r.(=) p.(=)