Variant #0001301955 (NC_000014.8:g.19378555G>A, NM_001013354.1:c.962G>A (OR11H12))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.19378555G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OR11H12_000029
Frequency 4/11404
Freq. EA 2/7766
Freq. AA 2/3638
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 16:41:19 +02:00 (CEST)
Date last edited 2014-05-03 19:40:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
OR11H12 NM_001013354.1 ?/? c.962G>A r.(?) p.(Gly321Glu)