Variant #0001302018 (NC_000014.8:g.20215682_20215683insT, NM_172194.1:c.96_97insT (OR4Q3))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.20215682_20215683insT
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OR4Q3_000005
Frequency 2/12518
Freq. EA 1/8254
Freq. AA 1/4264
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 2014-05-04 13:11:08 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
OR4Q3 NM_172194.1 ?/? c.96_97insT r.(?) p.(Tyr35Leufs*37)