Variant #0000960965 (NC_000009.11:g.139923265A>G, NC_000009.11(NM_001606.4):c.-673T>C (ABCA2))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.139923265A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID C9orf139_000007
Frequency 9137/11848
Freq. EA 5991/8146
Freq. AA 3146/3702
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 16:29:58 +02:00 (CEST)
Date last edited 2018-08-23 00:13:40 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA2 NM_001606.4 ?/? c.-673T>C r.(=) p.(=)
C9orf139 NM_207511.1 ?/? c.-1067+902A>G r.(=) p.(=)