Variant #0001820588 (NC_000019.9:g.58861838T>C, NM_130786.3:c.1090A>G (A1BG))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.58861838T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A1BG_000028
Frequency 12/12720
Freq. EA 0/8432
Freq. AA 12/4288
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 05:20:37 +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.1090A>G r.(?) p.(Ile364Val)