Variant #0001681315 (NC_000019.9:g.110783C>A, NM_001005240.1:c.105C>A (OR4F17))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.110783C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OR4F17_000005
Frequency 8/9612
Freq. EA 7/6492
Freq. AA 1/3120
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 16:26:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
OR4F17 NM_001005240.1 ?/? c.105C>A r.(?) p.(Asn35Lys)