Product Details

SNP ID

rs3009552

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.10:72704105 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

GAAGAATTTCAAGTGGGAGAATCAG[A/G]TGATCAGGTAGGTAACGCTGGCAGC

Phenotype

MIM: 614197

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MCU PubMed Links

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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