Product Details

SNP ID

rs7929532

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:89405826 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAGTACTTAAGTATCTCCCAACACA[A/G]TAATGTCAGTCTGCAGAGCTGGGAC

Phenotype

MIM: 605261

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

NOX4 PubMed Links

Additional Information

For this assay, SNP(s) [rs74356100] 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

NOX4

Gene Name

NADPH oxidase 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001143836.2		Intron			NP_001137308.1
NM_001143837.1		Intron			NP_001137309.1
NM_001291926.1		Intron			NP_001278855.1
NM_001291927.1		Intron			NP_001278856.1
NM_001291929.1		Intron			NP_001278858.1
NM_001300995.1		Intron			NP_001287924.1
NM_016931.4		Intron			NP_058627.1
XM_006718849.3		Intron			XP_006718912.1
XM_011542857.2		Intron			XP_011541159.1
XM_017017841.1		Intron			XP_016873330.1
XM_017017842.1		Intron			XP_016873331.1
XM_017017843.1		Intron			XP_016873332.1
XM_017017844.1		Intron			XP_016873333.1
XM_017017845.1		Intron			XP_016873334.1

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