Product Details

SNP ID

rs2413426

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:36861813 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTTTTGATCGCTGCTGTATCACTAG[A/G]AGGTAGCTCATCCCTATTGAGCACC

Phenotype

MIM: 601488

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

NCF4 PubMed Links

Additional Information

For this assay, SNP(s) [rs11912791] 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

NCF4

Gene Name

neutrophil cytosolic factor 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000631.4	578	Intron			NP_000622.2
NM_013416.3	578	Intron			NP_038202.2
XM_017028808.1	578	UTR 5			XP_016884297.1

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