Variant #0011147398 (NC_000019.9:g.107456T>C, NM_001005240.1:c.-3223T>C (OR4F17))

Chromosome 19
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.107456T>C
DB-ID -
dbSNP ID rs752811962
gnomAD frequency 1/54222
gnomAD homozygote count 0/15991
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     
OR4F17 NM_001005240.1 ./. c.-3223T>C r.(=) p.(=)