Product Details

SNP ID
rs17246626
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:52265514 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAAGATACAGTTGATGGTTGTCCTT[G/T]AGGGATAGAGTTACAATTGATTTTA
Phenotype
MIM: 602693
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
MCM3 PubMed Links
Additional Information
For this assay, SNP(s) [rs148804592] are located under a probe 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
MCM3
Gene Name
minichromosome maintenance complex component 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001270472.1 Intron NP_001257401.1
NM_002388.4 Intron NP_002379.3

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