Product Details

SNP ID

rs7252419

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:53995037 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTATGAGTCGTTATTATCACTCCC[A/G]TTCTAGAGAAGAGAAAAATGAGGGG

Phenotype

MIM: 606898 MIM: 606900

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CACNG6 PubMed Links

Additional Information

For this assay, SNP(s) [rs117326757] 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

CACNG6

Gene Name

calcium voltage-gated channel auxiliary subunit gamma 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_031897.2		Intron			NP_114103.2
NM_145814.1		Intron			NP_665813.1
NM_145815.1		Intron			NP_665814.1
XM_006723316.3		Intron			XP_006723379.1

Gene

CACNG8

Gene Name

calcium voltage-gated channel auxiliary subunit gamma 8

There are no transcripts associated with this gene.

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