Variant #0001820622 (NC_000019.9:g.58863753G>A, NM_130786.3:c.509C>T (A1BG))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.58863753G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A1BG_000062
Frequency 46/13006
Freq. EA 0/8600
Freq. AA 46/4406
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 2018-08-22 05:13:41 +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.509C>T r.(?) p.(Ala170Val)
A1BG-AS1 NR_015380.1 ?/? n.418G>A r.(?) p.(Ala170Val)