Variant #0001659787 (NC_000018.9:g.19236993_19236994del, NC_000018.9(NM_138340.4):c.892-7_892-6del (ABHD3))

Chromosome 18
DNA change (genomic) (Relative to hg19 / GRCh37) g.19236993_19236994del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABHD3_000013
Frequency 29/12518
Freq. EA 18/8254
Freq. AA 11/4264
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 16:45:07 +02:00 (CEST)
Date last edited 2018-08-23 13:28:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABHD3 NM_138340.4 ?/? c.892-7_892-6del r.(=) p.(=)