Variant #0001185239 (NC_000012.11:g.22089465A>G, NC_000012.11(NM_005691.2):c.142+2T>C (ABCC9))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.22089465A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCC9_000278
Frequency 1/13004
Freq. EA 1/8598
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 09:24:12 +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.142+2T>C r.spl? p.?