Variant #0001185183 (NC_000012.11:g.22063797G>A, NM_005691.2:c.1127C>T (ABCC9))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.22063797G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC9_000222
Frequency 1/13002
Freq. EA 1/8596
Freq. AA 0/4406
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 16:39:18 +02:00 (CEST)
Date last edited 2018-08-23 00:04:37 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC9 NM_005691.2 ?/? c.1127C>T r.(?) p.(Thr376Ile)