Product Details

SNP ID

rs11665792

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.19:53608356 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TGTGCAGATCTCCCTTGATGAAGCC[A/G]GAGAAGATGACGCAGCTCAGAACCA

Phenotype

MIM: 611165

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DPRX PubMed Links

Additional Information

For this assay, SNP(s) [rs12608484] 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

DPRX

Gene Name

divergent-paired related homeobox

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012728.1		Intron			NP_001012746.1
XM_011527011.2		Intron			XP_011525313.1
XM_011527012.2		Intron			XP_011525314.1

Gene

LOC284379

Gene Name

solute carrier family 7 member 3 pseudogene

There are no transcripts associated with this gene.

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