Product Details

SNP ID

rs34536102

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:1823404 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCCGTCCCAACCTAGCTCTCTGCA[A/G]TGAGTGAGTGCGTGCGGCTGTTCCG

Phenotype

MIM: 608171

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CACNA2D4 PubMed Links

Additional Information

For this assay, SNP(s) [rs143159259] 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

CACNA2D4

Gene Name

calcium voltage-gated channel auxiliary subunit alpha2delta 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_172364.4		Intron			NP_758952.4
XM_011521041.2		Intron			XP_011519343.1

Gene

LRTM2

Gene Name

leucine rich repeats and transmembrane domains 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001039029.2		Intron			NP_001034118.1
NM_001163925.1		Intron			NP_001157397.1
NM_001163926.1		Intron			NP_001157398.1
XM_011521015.1		Intron			XP_011519317.1
XM_017019848.1		Intron			XP_016875337.1

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