rs267606894
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF.
|
15767514 |
2005 |
rs267606894
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs267606894
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS.
|
9299505 |
1997 |
rs267606894
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Is the mitochondrial complex I ND5 gene a hot-spot for MELAS causing mutations?
|
12509858 |
2003 |
rs267606894
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease.
|
17400793 |
2007 |
rs267606895
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF.
|
15767514 |
2005 |
rs267606895
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease.
|
17400793 |
2007 |
rs267606895
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS.
|
9299505 |
1997 |
rs267606895
|
|
C |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs267606895
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Is the mitochondrial complex I ND5 gene a hot-spot for MELAS causing mutations?
|
12509858 |
2003 |
rs267606897
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS.
|
9299505 |
1997 |
rs267606897
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Is the mitochondrial complex I ND5 gene a hot-spot for MELAS causing mutations?
|
12509858 |
2003 |
rs267606897
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs267606897
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF.
|
15767514 |
2005 |
rs267606897
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease.
|
17400793 |
2007 |
rs267606898
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Is the mitochondrial complex I ND5 gene a hot-spot for MELAS causing mutations?
|
12509858 |
2003 |
rs267606898
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS.
|
9299505 |
1997 |
rs267606898
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease.
|
17400793 |
2007 |
rs267606898
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF.
|
15767514 |
2005 |
rs267606898
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs267606896
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs199476107
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome.
|
11781695 |
2001 |
rs199476107
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs121434453
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Segregation patterns of a novel mutation in the mitochondrial tRNA glutamic acid gene associated with myopathy and diabetes mellitus.
|
7726154 |
1995 |
rs387906421
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy.
|
19720722 |
2009 |