Product Details

SNP ID

rs141617289

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:29462389 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGTCCAGTGTCATCTTCGTGGTTG[C/T]GCCTCTCAGCCTCATCCTTGCCTCT

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

OR2H1 PubMed Links

Additional Information

For this assay, SNP(s) [rs2073148] are located under a probe 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

OR2H1

Gene Name

olfactory receptor family 2 subfamily H member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318014.1	2362	Missense Mutation	GCG,GTG	A207V	NP_001304943.1
NM_001318022.1	2362	Missense Mutation	GCG,GTG	A207V	NP_001304951.1
NM_030883.4	2362	Missense Mutation	GCG,GTG	A207V	NP_112145.1
XM_011514470.2	2362	Missense Mutation	GCG,GTG	A207V	XP_011512772.1
XM_011514472.2	2362	Missense Mutation	GCG,GTG	A207V	XP_011512774.1
XM_011514473.2	2362	Missense Mutation	GCG,GTG	A207V	XP_011512775.1
XM_011514479.2	2362	Missense Mutation	GCG,GTG	A207V	XP_011512781.1
XM_011514483.2	2362	Missense Mutation	GCG,GTG	A207V	XP_011512785.1
XM_011514484.2	2362	Missense Mutation	GCG,GTG	A207V	XP_011512786.1
XM_017010737.1	2362	Missense Mutation	GCG,GTG	A207V	XP_016866226.1
XM_017010738.1	2362	Missense Mutation	GCG,GTG	A207V	XP_016866227.1
XM_017010739.1	2362	Missense Mutation	GCG,GTG	A207V	XP_016866228.1
XM_017010740.1	2362	Missense Mutation	GCG,GTG	A129V	XP_016866229.1

Gene

OR5V1

Gene Name

olfactory receptor family 5 subfamily V member 1

There are no transcripts associated with this gene.

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