Product Details

SNP ID

rs28383613

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:3006138 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCACTGATCCCCCAGCCTTCTGCTC[C/G]ATCTACGGGGAAAACTGGGGAAGGC

Phenotype

MIM: 160998

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

NQO2 PubMed Links

Additional Information

For this assay, SNP(s) [rs576144322] 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

NQO2

Gene Name

NAD(P)H quinone dehydrogenase 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000904.4		Intron			NP_000895.2
NM_001290221.1		Intron			NP_001277150.1
NM_001290222.1		Intron			NP_001277151.1
NM_001318940.1		Intron			NP_001305869.1

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