Product Details

SNP ID

rs16865910

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:224380560 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTCACTGGATGTTGTAAATGATAT[A/G]TTTATTAGCAACCATGTAAAAAAAG

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FAM124B PubMed Links

Additional Information

For this assay, SNP(s) [rs144467311] 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

FAM124B

Gene Name

family with sequence similarity 124 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001122779.1		Intron			NP_001116251.1
NM_024785.2		Intron			NP_079061.2

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