Product Details

SNP ID

rs231461

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:43955675 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTTCAAGAACCCCAGTCTCAAAGGA[A/G]AGATATGGCCATGTCATAGGGGAGC

Phenotype

MIM: 600781

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

PYY PubMed Links

Additional Information

For this assay, SNP(s) [rs80089203] 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

PYY

Gene Name

peptide YY

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004160.5		Intron			NP_004151.3
XM_011525035.1		Intron			XP_011523337.1

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