Product Details

SNP ID

rs201960679

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:23521098 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGAACAGCAAATTTACTGAATGCA[A/G]GTGGCTCAGAGCAGGCTCAGAAACC

Phenotype

MIM: 609760

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

PRDM9 PubMed Links

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	615	Intron			NP_001297143.1
NM_020227.3	615	Missense Mutation	AGT,GGT	S143G	NP_064612.2

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