Product Details

SNP ID

rs116880118

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:66877471 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATATGATGCAAGGAATTGTGATTGC[A/C]ATGACAACTATAACCAAGTATACAC

Phenotype

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

MCMDC2 PubMed Links

Additional Information

For this assay, SNP(s) [rs16933088] 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

MCMDC2

Gene Name

minichromosome maintenance domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136160.1	538	Silent Mutation	GCA,GCC	A136A	NP_001129632.1
NM_001136161.1	538	Silent Mutation	GCA,GCC	A136A	NP_001129633.1
NM_173518.4	538	Silent Mutation	GCA,GCC	A136A	NP_775789.3
XM_005251174.2	538	Silent Mutation	GCA,GCC	A73A	XP_005251231.1
XM_006716427.3	538	Silent Mutation	GCA,GCC	A118A	XP_006716490.1
XM_006716429.2	538	Silent Mutation	GCA,GCC	A136A	XP_006716492.1
XM_006716433.3	538	Intron			XP_006716496.1
XM_011517467.2	538	Silent Mutation	GCA,GCC	A136A	XP_011515769.1
XM_011517468.2	538	Silent Mutation	GCA,GCC	A136A	XP_011515770.1
XM_011517469.2	538	Silent Mutation	GCA,GCC	A136A	XP_011515771.1
XM_017013140.1	538	Intron			XP_016868629.1

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