Product Details

SNP ID

rs146895917

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:116792608 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCATTGTAATTCTCATATTTGCCT[G/T]TGAAAGCAAATATGAAGCAAATGAA

Phenotype

MIM: 613572

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

GPRC6A PubMed Links

Additional Information

For this assay, SNP(s) [rs368671066] are located under a probe 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

GPRC6A

Gene Name

G protein-coupled receptor class C group 6 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286354.1	2359	Missense Mutation	AAA,ACA	K597T	NP_001273283.1
NM_001286355.1	2359	Missense Mutation	AAA,ACA	K701T	NP_001273284.1
NM_148963.3	2359	Missense Mutation	AAA,ACA	K772T	NP_683766.2
XM_017010475.1	2359	Missense Mutation	AAA,ACA	K725T	XP_016865964.1
XM_017010476.1	2359	Intron			XP_016865965.1

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