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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