Product Details

SNP ID

rs16991585

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.20:5953937 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCCATCAATAGAATCTGTTTCATG[A/G]ATGATCTTTTGTTCCTTTAGGATGT

Phenotype

MIM: 608187

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

MCM8 PubMed Links

Additional Information

For this assay, SNP(s) [rs116531606] 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

MCM8

Gene Name

minichromosome maintenance 8 homologous recombination repair factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001281520.1		Intron			NP_001268449.1
NM_001281521.1		Intron			NP_001268450.1
NM_001281522.1		Intron			NP_001268451.1
NM_032485.5		Intron			NP_115874.3
NM_182802.2		Intron			NP_877954.1
XM_011529387.2		Intron			XP_011527689.1
XM_017028105.1		Intron			XP_016883594.1
XM_017028106.1		Intron			XP_016883595.1
XM_017028107.1		Intron			XP_016883596.1

Gene

TRMT6

Gene Name

tRNA methyltransferase 6

There are no transcripts associated with this gene.

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