Product Details

SNP ID

rs147741332

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:57387817 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGGGCTGGTGAGCAGCCCAGTATG[C/T]AAAGTTCCAGCGGCTGCCGTCAACC

Phenotype

MIM: 605601 MIM: 606814

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PRG2 PubMed Links

Additional Information

For this assay, SNP(s) [rs630396] are located under a probe 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

PRG2

Gene Name

proteoglycan 2, pro eosinophil major basic protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001243245.2	734	Missense Mutation	ACG,GCG	T172A	NP_001230174.1
NM_001302926.1	734	Missense Mutation	ACG,GCG	T183A	NP_001289855.1
NM_001302927.1	734	Missense Mutation	ACG,GCG	T183A	NP_001289856.1
NM_002728.5	734	Missense Mutation	ACG,GCG	T183A	NP_002719.3

Gene

PRG3

Gene Name

proteoglycan 3, pro eosinophil major basic protein 2

There are no transcripts associated with this gene.

View Full Product Details