Product Details

SNP ID

rs3009553

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:72703050 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GACTGGAAAAGTGTGGTCAGCATTC[C/T]GGGCAGCACCAATCTGACATGACCT

Phenotype

MIM: 614197

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MCU PubMed Links

Additional Information

For this assay, SNP(s) [rs74321992] 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

MCU

Gene Name

mitochondrial calcium uniporter

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001270679.1		Intron			NP_001257608.1
NM_001270680.1		Intron			NP_001257609.1
NM_138357.2		Intron			NP_612366.1
XM_017016882.1		Intron			XP_016872371.1

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