Variant #0001820589 (NC_000019.9:g.58861859C>T, NM_130786.3:c.1069G>A (A1BG))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.58861859C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A1BG_000029
Frequency 2/12666
Freq. EA 0/8396
Freq. AA 2/4270
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 2018-08-22 05:13:47 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
A1BG NM_130786.3 ?/? c.1069G>A r.(?) p.(Ala357Thr)