Variant #0001659832 (NC_000018.9:g.19284446T>G, NC_000018.9(NM_138340.4):c.162+19A>C (ABHD3))

Chromosome 18
DNA change (genomic) (Relative to hg19 / GRCh37) g.19284446T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD3_000058
Frequency 1/12570
Freq. EA 0/8332
Freq. AA 1/4238
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 16:45:07 +02:00 (CEST)
Date last edited 2018-08-23 04:29:06 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABHD3 NM_138340.4 ?/? c.162+19A>C r.(=) p.(=)