Variant #0001308378 (NC_000014.8:g.23067296G>A, NC_000014.8(NM_022060.2):c.23+58G>A (ABHD4))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.23067296G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD4_000005
Frequency 128/4566
Freq. EA 123/3182
Freq. AA 5/1384
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 10:11:40 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABHD4 NM_022060.2 ?/? c.23+58G>A r.(=) p.(=)