Product Details

SNP ID
rs200386479
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.5:23524417 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGCAGATCTTCTATAGAACCTGCC[A/G]AGTCATTAGGCCAGGCTGTGAACTG
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 1222 Intron NP_001297143.1
NM_020227.3 1222 Missense Mutation CAA,CGA Q345R NP_064612.2

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