Product Details

SNP ID
rs3793782
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:72710515 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GATGGGAATGCTGTCAAAGGAGCTC[A/G]CTTGGAAAGGCCATTCCATCACCTA
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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