Variant #0000497222 (NC_000004.11:g.89052998G>T, NM_004827.2:c.335C>A (ABCG2))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.89052998G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCG2_000109
Frequency 5/13006
Freq. EA 5/8600
Freq. AA 0/4406
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 2023-07-13 22:18:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCG2 NM_004827.2 ?/? c.335C>A r.(?) p.(Pro112Gln)