Product Details

SNP ID

rs7797481

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.7:104129609 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TGCCACACATCCGAAAGATAATTTT[C/G]TGCTTTAAAGTACTTGAAGACAAAC

Phenotype

MIM: 602331

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

ORC5 PubMed Links

Additional Information

For this assay, SNP(s) [rs28645598] 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

ORC5

Gene Name

origin recognition complex subunit 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002553.3		Intron			NP_002544.1
NM_181747.3		Intron			NP_859531.1
XM_011516273.2		Intron			XP_011514575.1

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