Variant #0000000413 (NC_000001.10:g.69428T>G, NM_001005484.1:c.338T>G (OR4F5))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.69428T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OR4F5_000001
Frequency 327/10670
Freq. EA 313/6848
Freq. AA 14/3822
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 2014-04-28 05:10:47 +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.338T>G r.(?) p.(Phe113Cys)