Variant #0005390242 (NC_000008.10:g.116680G>A, NM_001005504.1:c.345C>T (OR4F21))

Chromosome 8
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.116680G>A
DB-ID -
dbSNP ID rs201925745
gnomAD frequency 16/25370
gnomAD homozygote count 2/12671
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
OR4F21 NM_001005504.1 ./. c.345C>T r.(?) p.(Leu115=)