Variant #0001467764 (NC_000016.9:g.16130342G>T, NM_004996.3:c.691G>T (ABCC1))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.16130342G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC1_000041
Frequency 7/12072
Freq. EA 6/8256
Freq. AA 1/3816
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 23:38:38 +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.691G>T r.(?) p.(Gly231Cys)