Product Details

SNP ID

rs11012808

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:18148703 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATACTCTTTTCTGTTCATTTAAAAA[C/T]GGTACTGGAGGCTGGACATGGTAGC

Phenotype

MIM: 600003

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CACNB2 PubMed Links

Additional Information

For this assay, SNP(s) [rs142355845] 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

CACNB2

Gene Name

calcium voltage-gated channel auxiliary subunit beta 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000724.3		Intron			NP_000715.2
NM_001167945.1		Intron			NP_001161417.1
NM_201570.2		Intron			NP_963864.1
NM_201571.3		Intron			NP_963865.2
NM_201572.3		Intron			NP_963866.2
NM_201590.2		Intron			NP_963884.2
NM_201593.2		Intron			NP_963887.2
NM_201596.2		Intron			NP_963890.2
NM_201597.2		Intron			NP_963891.1
XM_005252588.3		Intron			XP_005252645.1
XM_005252591.3		Intron			XP_005252648.1
XM_006717502.3		Intron			XP_006717565.1
XM_011519659.2		Intron			XP_011517961.1
XM_011519660.2		Intron			XP_011517962.1
XM_017016625.1		Intron			XP_016872114.1

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