Variant #0001681311 (NC_000019.9:g.110687T>A, NM_001005240.1:c.9T>A (OR4F17))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.110687T>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OR4F17_000001
Frequency 1/12996
Freq. EA 1/8592
Freq. AA 0/4404
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 16:45:39 +02:00 (CEST)
Date last edited 2014-05-04 16:15:41 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
OR4F17 NM_001005240.1 ?/? c.9T>A r.(=) p.(=)