Variant #0001820658 (NC_000019.9:g.58864655_58864656del, NC_000019.9(NM_130786.3):c.70+2_70+3del (A1BG))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.58864655_58864656del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A1BG_000098
Frequency 44/12514
Freq. EA 30/8252
Freq. AA 14/4262
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 2024-04-28 19:03:22 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
A1BG NM_130786.3 ?/? c.70+2_70+3del r.spl? p.?
A1BG-AS1 NR_015380.1 ?/? n.1076-90_1076-89del r.(=) p.(=)