Product Details

SNP ID

rs150356042

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:132617677 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCATAGGCCTCTGAGAAGACCACCC[C/T]GAAGGCAAATGCTCCAGGGACCGAC

Phenotype

MIM: 604849

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

TAAR2 PubMed Links

Additional Information

For this assay, SNP(s) [rs61745666] 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

TAAR2

Gene Name

trace amine associated receptor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001033080.1	417	Missense Mutation	AGG,GGG	R177G	NP_001028252.1
NM_014626.3	417	Missense Mutation	AGG,GGG	R132G	NP_055441.2

Gene

TAAR3

Gene Name

trace amine associated receptor 3 (gene/pseudogene)

There are no transcripts associated with this gene.

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