Product Details

SNP ID

rs75246452

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:134741130 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AACTGAACTCCCTCAGCGTTCCTTC[C/T]GTTTCAAAGCGAGTAGTGCTGGGTG

Phenotype

MIM: 601118

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CAMLG PubMed Links

Additional Information

For this assay, SNP(s) [rs12657663] are located under a probe 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

CAMLG

Gene Name

calcium modulating ligand

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001745.3	934	Silent Mutation	TCC,TCT	S80S	NP_001736.1
XM_011543653.1	934	Silent Mutation	TCC,TCT	S80S	XP_011541955.1

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