Variant #0000497163 (NC_000004.11:g.89028436_89028438del, NC_000004.11(NM_004827.2):c.1195-20_1195-18del (ABCG2))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.89028436_89028438del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCG2_000048
Frequency 22/12516
Freq. EA 9/8250
Freq. AA 13/4266
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 22:25:19 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCG2 NM_004827.2 ?/? c.1195-20_1195-18del r.(=) p.(=)