Product Details

SNP ID

rs7961709

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:71447583 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCTATATGCACATTTTCCACACACT[C/T]ATTTTATCCTTCTTGCCTTCAGAAG

Phenotype

MIM: 606667

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

LGR5 PubMed Links

Additional Information

For this assay, SNP(s) [rs75729588,rs79684406] 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

LGR5

Gene Name

leucine rich repeat containing G protein-coupled receptor 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001277226.1		Intron			NP_001264155.1
NM_001277227.1		Intron			NP_001264156.1
NM_003667.3		Intron			NP_003658.1

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