Product Details

SNP ID

rs60344499

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:143935266 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGATAACCAGACGTGGGTGAGAGAA[A/T]TTATTCTCCTTGGCTTATCCAGTGA

Phenotype

MIM: 608497

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

OR2F1 PubMed Links

Additional Information

For this assay, SNP(s) [rs2240358] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

OR2F1

Gene Name

olfactory receptor family 2 subfamily F member 1 (gene/pseudogene)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012369.2	34	Intron			NP_036501.2
XM_011516019.2	34	Intron			XP_011514321.1
XM_011516020.2	34	Intron			XP_011514322.1

Gene

OR2F2

Gene Name

olfactory receptor family 2 subfamily F member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004685.1	34	Missense Mutation	ATT,TTT	I12F	NP_001004685.1

View Full Product Details