Variant #0001467734 (NC_000016.9:g.16103682C>T, NM_004996.3:c.275C>T (ABCC1))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.16103682C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC1_000011
Frequency 19/12048
Freq. EA 0/8224
Freq. AA 19/3824
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 13:38:24 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC1 NM_004996.3 ?/? c.275C>T r.(?) p.(Ser92Phe)