Variant #0005390258 (NC_000008.10:g.117033C>T, NM_001005504.1:c.-9G>A (OR4F21))

Chromosome 8
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.117033C>T
DB-ID -
dbSNP ID rs200431102
gnomAD frequency 126/192
gnomAD homozygote count 31/1
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.-9G>A r.(=) p.(=)