Variant #0001462340 (NC_000016.9:g.8829558T>C, NM_020686.5:c.-39T>C (ABAT))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.8829558T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABAT_000001
Frequency 1/12984
Freq. EA 0/8594
Freq. AA 1/4390
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 03:36:30 +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.-39T>C r.(=) p.(=)