Variant #0001820586 (NC_000019.9:g.58861808A>G, NM_130786.3:c.1120T>C (A1BG))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.58861808A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A1BG_000026
Frequency 62/12628
Freq. EA 56/8366
Freq. AA 6/4262
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 05:15:36 +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.1120T>C r.(?) p.(Cys374Arg)