Variant #0001467793 (NC_000016.9:g.16138558G>T, NC_000016.9(NM_004996.3):c.1040+21G>T (ABCC1))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.16138558G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC1_000070
Frequency 2/12048
Freq. EA 0/8246
Freq. AA 2/3802
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 08:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC1 NM_004996.3 ?/? c.1040+21G>T r.(=) p.(=)