Variant #0001900096 (NC_000022.10:g.16449612A>G, NM_001005239.1:c.193T>C (OR11H1))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.16449612A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OR11H1_000012
Frequency 29/9324
Freq. EA 7/6322
Freq. AA 22/3002
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 16:50:05 +02:00 (CEST)
Date last edited 2014-05-04 16:40:29 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
OR11H1 NM_001005239.1 ?/? c.193T>C r.(?) p.(Trp65Arg)