Variant #0000809665 (NC_000008.10:g.116897del, NM_001005504.1:c.128del (OR4F21))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.116897del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OR4F21_000002
Frequency 24/2840
Freq. EA 14/1126
Freq. AA 10/1714
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 16:29:29 +02:00 (CEST)
Date last edited 2014-05-04 16:40:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
OR4F21 NM_001005504.1 ?/? c.128del r.(?) p.(Ile43Thrfs*7)