Variant #0000960961 (NC_000009.11:g.139923138A>T, NC_000009.11(NM_001606.4):c.-546T>A (ABCA2))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.139923138A>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID C9orf139_000001
Frequency 1/11804
Freq. EA 1/8116
Freq. AA 0/3688
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 13:02:00 +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.-546T>A r.(=) p.(=)
C9orf139 NM_207511.1 ?/? c.-1067+775A>T r.(=) p.(=)