Product Details

SNP ID

rs6499511

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:71368704 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCTACTCTGCCATGCCCGTGTGTC[C/T]GGAAAGATTATGTGTGGGTTCATTT

Phenotype

MIM: 114051

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CALB2 PubMed Links

Additional Information

For this assay, SNP(s) [rs78697599] 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

CALB2

Gene Name

calbindin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001740.4		Intron			NP_001731.2
NM_007088.3		Intron			NP_009019.1

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