Product Details

SNP ID

rs200008043

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:23521083 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTGAAAGAATTGTCAAGAACAGCA[A/C]ATTTACTGAATGCAAGTGGCTCAGA

Phenotype

MIM: 609760

Polymorphism

A/C, Transversion 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	600	Intron			NP_001297143.1
NM_020227.3	600	Missense Mutation	AAT,CAT	N138H	NP_064612.2

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