Variant #0001820616 (NC_000019.9:g.58863078G>T, NC_000019.9(NM_130786.3):c.614-25C>A (A1BG))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.58863078G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A1BG_000056
Frequency 1/12930
Freq. EA 1/8558
Freq. AA 0/4372
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 05:15:56 +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.614-25C>A r.(=) p.(=)