Product Details

SNP ID
rs7186210
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.16:24256090 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGGGGCAACAGGCGGGGAGCTGTC[C/T]CTTCAGCACCACGGACCTTGGCGCC
Phenotype
MIM: 606403
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
CACNG3 PubMed Links
Additional Information
For this assay, SNP(s) [rs138438483] 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
CACNG3
Gene Name
calcium voltage-gated channel auxiliary subunit gamma 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006539.3 538 UTR 5 NP_006530.1

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