Product Details

SNP ID
rs186596959
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:99607168 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGTCAGACCGCAGGGAGCCCGGGC[C/T]TAAGAAAAAGGTATTGACCATTCAG
Phenotype
MIM: 616741
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
PRDM13 PubMed Links

Gene Details

Gene
PRDM13
Gene Name
PR domain 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_021620.3 395 Missense Mutation CCT,CTT P45L NP_067633.2

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