Variant #0001900090 (NC_000022.10:g.16449076C>T, NM_001005239.1:c.729G>A (OR11H1))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.16449076C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OR11H1_000006
Frequency 22/12998
Freq. EA 0/8596
Freq. AA 22/4402
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 2014-03-29 21:01:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
OR11H1 NM_001005239.1 ?/? c.729G>A r.(?) p.(Met243Ile)