Product Details

SNP ID

rs12727187

Assay Type

Functionally Tested

NCBI dbSNP Submissions

14

Location

Chr.1:84310779 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATATTACCAACATTGAATTCAAAG[C/G]GGTTTTGCATAAATTGATAAGCAAC

Phenotype

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

SAMD13 PubMed Links

Additional Information

For this assay, SNP(s) [rs75697488] 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

SAMD13

Gene Name

sterile alpha motif domain containing 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010971.2		Intron			NP_001010971.1
NM_001134663.1		Intron			NP_001128135.1
NM_001134664.1		Intron			NP_001128136.1
XM_017000377.1		Intron			XP_016855866.1

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