Variant #0008638906 (NC_000014.8:g.19377739C>T, NM_001013354.1:c.146C>T (OR11H12))

Chromosome 14
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.19377739C>T
DB-ID -
dbSNP ID rs201865883
gnomAD frequency 23/243654
gnomAD homozygote count 3/121803
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     
OR11H12 NM_001013354.1 ./. c.146C>T r.(?) p.(Thr49Ile)