Variant #0001681313 (NC_000019.9:g.110747_110748insT, NM_001005240.1:c.69_70insT (OR4F17))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.110747_110748insT
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OR4F17_000003
Frequency 74/12140
Freq. EA 68/8004
Freq. AA 6/4136
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 2014-05-21 22:50:56 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
OR4F17 NM_001005240.1 ?/? c.69_70insT r.(?) p.(Val26Cysfs*20)