Variant #0001185222 (NC_000012.11:g.22078957C>T, NM_005691.2:c.325G>A (ABCC9))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.22078957C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC9_000261
Frequency 1/13006
Freq. EA 0/8600
Freq. AA 1/4406
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 01:51:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC9 NM_005691.2 ?/? c.325G>A r.(?) p.(Val109Met)