Product Details

SNP ID
rs11203826
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:17041671 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAAAGAAGATTAAATTTAAAGGAAA[A/G]AGAATAATTGATGTGATAAGGACCC
Phenotype
MIM: 610633
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MICU3 PubMed Links

Gene Details

Gene
MICU3
Gene Name
mitochondrial calcium uptake family member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_181723.2 Intron NP_859074.1
XM_005273477.2 Intron XP_005273534.1
XM_006716328.2 Intron XP_006716391.1
XM_006716329.2 Intron XP_006716392.1
XM_006716330.2 Intron XP_006716393.1
XM_006716333.3 Intron XP_006716396.1
XM_011544507.2 Intron XP_011542809.1
XM_011544508.2 Intron XP_011542810.1
XM_017013336.1 Intron XP_016868825.1
XM_017013337.1 Intron XP_016868826.1
XM_017013338.1 Intron XP_016868827.1
XM_017013339.1 Intron XP_016868828.1
XM_017013340.1 Intron XP_016868829.1
XM_017013341.1 Intron XP_016868830.1
XM_017013342.1 Intron XP_016868831.1
XM_017013343.1 Intron XP_016868832.1

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