Product Details

SNP ID

rs146876965

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:57378751 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTGCTAGTGCAGCACTGAATGCGA[C/T]AGTTGAAGTTGAAGTCATGGATAGA

Phenotype

MIM: 600843 MIM: 605601 MIM: 606814

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

P2RX3 PubMed Links

Additional Information

For this assay, SNP(s) [rs34108746] are located under a probe and SNP(s) [rs1940145] 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

P2RX3

Gene Name

purinergic receptor P2X 3

There are no transcripts associated with this gene.

Gene

PRG2

Gene Name

proteoglycan 2, pro eosinophil major basic protein

There are no transcripts associated with this gene.

Gene

PRG3

Gene Name

proteoglycan 3, pro eosinophil major basic protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006093.3	547	Missense Mutation	TAT,TGT	Y146C	NP_006084.2

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