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

View Full Product Details