Product Details

SNP ID

rs2147279

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.10:13170884 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CTAAAGTTGAATGTTTGGAATTAGC[C/T]GTGCTTATTCTCTGTCCTTTCTCTT

Phenotype

MIM: 609357

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MCM10 PubMed Links

Additional Information

For this assay, SNP(s) [rs116353713,rs75610705] are located under a primer 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

MCM10

Gene Name

minichromosome maintenance 10 replication initiation factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018518.4		Intron			NP_060988.3
NM_182751.2		Intron			NP_877428.1
XM_011519538.2		Intron			XP_011517840.1

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