Variant #0001462432 (NC_000016.9:g.8862785G>C, NM_020686.5:c.771G>C (ABAT))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.8862785G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABAT_000093
Frequency 1/12994
Freq. EA 1/8600
Freq. AA 0/4394
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 16:42:42 +02:00 (CEST)
Date last edited 2018-08-23 10:40:37 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABAT NM_020686.5 ?/? c.771G>C r.(?) p.(Glu257Asp)