Variant #0011147440 (NC_000019.9:g.110685A>C, NM_001005240.1:c.7A>C (OR4F17))

Chromosome 19
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.110685A>C
DB-ID -
dbSNP ID rs757221224
gnomAD frequency 1/245902
gnomAD homozygote count 0/122950
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
OR4F17 NM_001005240.1 ./. c.7A>C r.(?) p.(Thr3Pro)