Variant #0001820666 (NC_000019.9:g.58864766T>C, NC_000019.9(NM_130786.3):c.34+4A>G (A1BG))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.58864766T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A1BG_000106
Frequency 1/12996
Freq. EA 1/8594
Freq. AA 0/4402
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 2018-08-23 07:33:50 +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.34+4A>G N/A N/A
A1BG-AS1 NR_015380.1 ?/? n.1097T>C N/A N/A