Variant #0001467761 (NC_000016.9:g.16130339C>T, NM_004996.3:c.688C>T (ABCC1))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.16130339C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC1_000038
Frequency 1/12074
Freq. EA 1/8258
Freq. AA 0/3816
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 2018-08-23 09:40:14 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC1 NM_004996.3 ?/? c.688C>T r.(?) p.(Arg230Trp)