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SNP ID

rs201009703

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:104617636 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGGAACTCATTGCCTGAGATGTCA[G/T]CACAGGCCAACTTCATGACAGCTAG

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

OR13C9 PubMed Links

Gene Details

Gene

OR13C9

Gene Name

olfactory receptor family 13 subfamily C member 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001001956.1	569	Missense Mutation	GAT,GCT	D190A	NP_001001956.1

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