Variant #0001427321 (NC_000015.9:g.89736558T>C, NC_000015.9(NM_007011.7):c.1081+8T>C (ABHD2))

Chromosome 15
DNA change (genomic) (Relative to hg19 / GRCh37) g.89736558T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD2_000067
Frequency 5112/12998
Freq. EA 3525/8598
Freq. AA 1587/4400
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 16:41:46 +02:00 (CEST)
Date last edited 2018-08-23 09:25:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABHD2 NM_007011.7 ?/? c.1081+8T>C r.(=) p.(=)