Product Details

SNP ID

rs149263533

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:184036512 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCCCTTCCATGGACAGAGGTGAAC[A/G]CTCTCCTTCAGCCCTTTCACCTACA

Phenotype

MIM: 610122

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

HTR3D PubMed Links

Additional Information

For this assay, SNP(s) [rs6443930] are located under a probe and SNP(s) [rs73183412] 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

HTR3D

Gene Name

5-hydroxytryptamine receptor 3D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145143.1	338	Missense Mutation	CAC,CGC	H112R	NP_001138615.1
NM_001163646.1	338	Intron			NP_001157118.1
NM_182537.2	338	Missense Mutation	CAC,CGC	H38R	NP_872343.2
XM_017005854.1	338	Intron			XP_016861343.1

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