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

View Full Product Details