Variant #0001837657 (NC_000020.10:g.25289033C>T, NC_000020.10(NM_015600.4):c.787+60G>A (ABHD12))

Chromosome 20
DNA change (genomic) (Relative to hg19 / GRCh37) g.25289033C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD12_000044
Frequency 11/4566
Freq. EA 0/3182
Freq. AA 11/1384
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 16:46:43 +02:00 (CEST)
Date last edited 2018-08-23 00:37:01 +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.787+60G>A r.(=) p.(=)