Product Details

SNP ID

rs76727787

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:104617699 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAATGATTGATGACATTCTTCCTG[C/A]AGAAAGGCAATTGTACTACAAATGT

Phenotype

Polymorphism

C/A, 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	506	Missense Mutation	TGC,TTC	C169F	NP_001001956.1

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