Variant #0001900098 (NC_000022.10:g.16449632C>A, NM_001005239.1:c.173G>T (OR11H1))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.16449632C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OR11H1_000014
Frequency 1/9322
Freq. EA 0/6320
Freq. AA 1/3002
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 2016-10-09 15:51:50 +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.173G>T r.(?) p.(Gly58Val)