Product Details

SNP ID

rs9590712

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.13:42783601 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGAGCTTTTCAGATTTTGGGCTTTT[A/G]GATTTGGGATGCTCAACTTGTATGA

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FAM216B PubMed Links

Additional Information

For this assay, SNP(s) [rs9594809] 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

FAM216B

Gene Name

family with sequence similarity 216 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318932.1		Intron			NP_001305861.1
NM_182508.2		Intron			NP_872314.1

View Full Product Details