Variant #0001681312 (NC_000019.9:g.110708C>G, NM_001005240.1:c.30C>G (OR4F17))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.110708C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OR4F17_000002
Frequency 7/13002
Freq. EA 7/8598
Freq. AA 0/4404
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 16:45:39 +02:00 (CEST)
Date last edited 2014-05-04 16:05:23 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
OR4F17 NM_001005240.1 ?/? c.30C>G r.(=) p.(=)