Product Details

SNP ID

rs2292276

Assay Type

Functionally Tested

NCBI dbSNP Submissions

75

Location

Chr.1:163322572 on Build GRCh38

Set Membership

HapMap JSNP

Context Sequence [VIC/FAM]

GCATGCATAACGCCATCATTGTTCC[C/T]TTTAAAAGTTCAAGGAACGTTTTAC

Phenotype

MIM: 611772 MIM: 603276

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

NUF2 PubMed Links

Additional Information

For this assay, SNP(s) [rs12755500] 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

NUF2

Gene Name

NUF2, NDC80 kinetochore complex component

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_031423.3		Intron			NP_113611.2
NM_145697.2		Intron			NP_663735.2
XM_011510036.1		Intron			XP_011508338.1

Gene

RGS5

Gene Name

regulator of G-protein signaling 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001195303.2		Intron			NP_001182232.1
NM_001254748.1		Intron			NP_001241677.1
NM_001254749.1		Intron			NP_001241678.1
NM_003617.3		Intron			NP_003608.1

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