Product Details

SNP ID

rs11065450

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:121141854 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGTTTAGGGAACACTCTGTGTTATG[A/C]GTTCCACCACACAATCCATGTCACA

Phenotype

MIM: 602566

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

P2RX7 PubMed Links

Additional Information

For this assay, SNP(s) [rs568531] 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

P2RX7

Gene Name

purinergic receptor P2X 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002562.5		Intron			NP_002553.3
XM_011538419.2		Intron			XP_011536721.1
XM_011538420.2		Intron			XP_011536722.1
XM_017019364.1		Intron			XP_016874853.1
XM_017019365.1		Intron			XP_016874854.1
XM_017019366.1		Intron			XP_016874855.1
XM_017019367.1		Intron			XP_016874856.1

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