Variant #0001727326 (NC_000019.9:g.13249098G>A, NM_052876.3:c.1462G>A (NACC1))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.13249098G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID NACC1_000069
Frequency 40/13006
Freq. EA 38/8600
Freq. AA 2/4406
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 16:45:39 +02:00 (CEST)
Date last edited 2013-05-05 23:29:44 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NACC1 NM_052876.3 ?/? c.1462G>A r.(?) p.(Ala488Thr)