Product Details

SNP ID

rs10088772

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:28025718 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCAGAGAGATGGAGAAGTGCAGAAC[A/G]GATTGTTAGAAGCAGCCATTGTGGC

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

NUGGC PubMed Links

Additional Information

For this assay, SNP(s) [rs116090651] 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

NUGGC

Gene Name

nuclear GTPase, germinal center associated

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010906.1		Intron			NP_001010906.1
XM_011544523.2		Intron			XP_011542825.1
XM_011544524.2		Intron			XP_011542826.1
XM_011544525.1		Intron			XP_011542827.1
XM_011544526.2		Intron			XP_011542828.1
XM_017013403.1		Intron			XP_016868892.1

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