Product Details

SNP ID

rs201590420

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:23510014 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGAAGATTCTGATGAAGAATGGAC[A/C]CCTAGGCAGCAAGGTAAGAGGGAAG

Phenotype

MIM: 609760

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

PRDM9 PubMed Links

Additional Information

For this assay, SNP(s) [rs2973615] 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

PRDM9

Gene Name

PR domain 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001310214.1	476	Intron			NP_001297143.1
NM_020227.3	476	Silent Mutation	ACA,ACC	T96T	NP_064612.2

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