Product Details

SNP ID

rs79977940

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:151294734 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAGGATGATGTTTGGCAAAGACAAA[A/C]CAGCCATGATCACCCAAACACAAAC

Phenotype

MIM: 606379 MIM: 611318

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

GPR87 PubMed Links

Additional Information

For this assay, SNP(s) [rs2242353] 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

GPR87

Gene Name

G protein-coupled receptor 87

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_023915.3	873	Missense Mutation	GGT,GTT	G171V	NP_076404.3

Gene

MED12L

Gene Name

mediator complex subunit 12 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_053002.5	873	Intron			NP_443728.3
XM_006713487.3	873	Intron			XP_006713550.1
XM_011512390.2	873	Intron			XP_011510692.1
XM_011512394.2	873	Intron			XP_011510696.1
XM_011512399.2	873	Intron			XP_011510701.1
XM_017005676.1	873	Intron			XP_016861165.1
XM_017005677.1	873	Intron			XP_016861166.1
XM_017005678.1	873	Intron			XP_016861167.1
XM_017005679.1	873	Intron			XP_016861168.1
XM_017005680.1	873	Intron			XP_016861169.1
XM_017005681.1	873	Intron			XP_016861170.1

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