Variant #0001467762 (NC_000016.9:g.16130340G>A, NM_004996.3:c.689G>A (ABCC1))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.16130340G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC1_000039
Frequency 32/12062
Freq. EA 0/8250
Freq. AA 32/3812
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 16:42:42 +02:00 (CEST)
Date last edited 2024-04-28 12:53:44 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC1 NM_004996.3 ?/? c.689G>A r.(?) p.(Arg230Gln)