Product Details

SNP ID

rs1418213

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:90741893 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGAGTTAACACAGAAAAGTACATAG[A/G]TGGGGAAATCACAGAGACCCTGCAG

Phenotype

MIM: 182137

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

HTR7 PubMed Links

Additional Information

For this assay, SNP(s) [rs56288532] 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

HTR7

Gene Name

5-hydroxytryptamine receptor 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000872.4	2174	UTR 3			NP_000863.1
NM_019859.3	2174	UTR 3			NP_062873.1
NM_019860.3	2174	UTR 3			NP_062874.1

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