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SNP ID

rs75216399

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:104598722 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAGGAAGGTTTGCTTCTCCCCTCC[G/A]AAGAGCTAATTTTGAAGATGCTCAA

Phenotype

Polymorphism

G/A, Transition substitution

Allele Nomenclature

Literature Links

OR13C2 PubMed Links

Gene Details

Gene

OR13C2

Gene Name

olfactory receptor family 13 subfamily C member 2

There are no transcripts associated with this gene.

Gene

OR13C5

Gene Name

olfactory receptor family 13 subfamily C member 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004482.1	692	Missense Mutation	TCG,TTG	S231L	NP_001004482.1

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