Product Details

SNP ID

rs1291350

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:12932606 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AATAAAGCCCAGGTGGAAACTACAA[C/T]GAAATGTTCCATTTGTAGCATATAC

Phenotype

MIM: 607437

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FAM234B PubMed Links

Additional Information

For this assay, SNP(s) [rs77563944] 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

FAM234B

Gene Name

family with sequence similarity 234 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020853.1		Intron			NP_065904.1
XM_017019706.1		Intron			XP_016875195.1

Gene

GPRC5D

Gene Name

G protein-coupled receptor class C group 5 member D

There are no transcripts associated with this gene.

View Full Product Details