Variant #0000497226 (NC_000004.11:g.89053657_89053658insC, NC_000004.11(NM_004827.2):c.263+70_263+71insG (ABCG2))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.89053657_89053658insC
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCG2_000113
Frequency 34/12520
Freq. EA 4/8254
Freq. AA 30/4266
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 16:25:12 +02:00 (CEST)
Date last edited 2025-01-02 20:53:51 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCG2 NM_004827.2 ?/? c.263+70_263+71insG r.(=) p.(=)