Variant #0008638892 (NC_000014.8:g.19377716C>T, NM_001013354.1:c.123C>T (OR11H12))

Chromosome 14
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.19377716C>T
DB-ID -
dbSNP ID rs747747275
gnomAD frequency 2/245170
gnomAD homozygote count 0/122583
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.123C>T r.(?) p.(Phe41=)