Product Details

SNP ID

rs141158932

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:104569364 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCATGTATTTCTTCCTCTGTAATC[C/T]TTCCTTCCTCGACGTTTGCTACACA

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

OR13C8 PubMed Links

Gene Details

Gene

OR13C8

Gene Name

olfactory receptor family 13 subfamily C member 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004483.1	197	Missense Mutation	CCT,CTT	P66L	NP_001004483.1

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