Variant #0001301931 (NC_000014.8:g.19377692T>C, NM_001013354.1:c.99T>C (OR11H12))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.19377692T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OR11H12_000005
Frequency 2/12990
Freq. EA 0/8592
Freq. AA 2/4398
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 2014-04-28 20:45:36 +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.99T>C r.(=) p.(=)