Variant #0001185198 (NC_000012.11:g.22065893A>G, NM_005691.2:c.924T>C (ABCC9))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.22065893A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC9_000243
Frequency 22/13006
Freq. EA 0/8600
Freq. AA 22/4406
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 05:20:07 +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.924T>C r.(=) p.(=)