Product Details

SNP ID

rs2962589

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:2709004 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCTCCAACCTGCTTCAAGCCCCAC[C/T]CCCAGAGGCCTTCTCCAGGCCACAT

Phenotype

MIM: 606198

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

IRX2 PubMed Links

Additional Information

For this assay, SNP(s) [rs115474012] 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

IRX2

Gene Name

iroquois homeobox 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001134222.1		Intron			NP_001127694.1
NM_033267.4		Intron			NP_150366.1
XM_011513979.2		Intron			XP_011512281.1

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