Variant #0000000415 (NC_000001.10:g.69496G>A, NM_001005484.1:c.406G>A (OR4F5))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.69496G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OR4F5_000003
Frequency 25/10574
Freq. EA 2/6766
Freq. AA 23/3808
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 16:20:35 +02:00 (CEST)
Date last edited 2014-04-19 04:05:22 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
OR4F5 NM_001005484.1 ?/? c.406G>A r.(?) p.(Gly136Ser)