Variant #0001301930 (NC_000014.8:g.19377691C>G, NM_001013354.1:c.98C>G (OR11H12))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.19377691C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OR11H12_000004
Frequency 1/12990
Freq. EA 1/8592
Freq. AA 0/4398
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 2014-05-02 16:11:10 +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.98C>G r.(?) p.(Thr33Ser)