rs797044951
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Clinical Phenotype of De Novo GNAO1 Mutation: Case Report and Review of Literature.
|
28503590 |
2019 |
rs886039494
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Clinical Phenotype of De Novo GNAO1 Mutation: Case Report and Review of Literature.
|
28503590 |
2019 |
rs797044951
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
GNAO1 encephalopathy: Broadening the phenotype and evaluating treatment and outcome.
|
28357411 |
2017 |
rs797044951
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Movement disorder in GNAO1 encephalopathy associated with gain-of-function mutations.
|
28747448 |
2017 |
rs886039494
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
GNAO1 encephalopathy: Broadening the phenotype and evaluating treatment and outcome.
|
28357411 |
2017 |
rs886039494
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Movement disorder in GNAO1 encephalopathy associated with gain-of-function mutations.
|
28747448 |
2017 |
rs797044951
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Clinical Course of Six Children With GNAO1 Mutations Causing a Severe and Distinctive Movement Disorder.
|
27068059 |
2016 |
rs797044951
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Phenotypic spectrum of GNAO1 variants: epileptic encephalopathy to involuntary movements with severe developmental delay.
|
25966631 |
2016 |
rs797044951
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Progressive Movement Disorder in Brothers Carrying a GNAO1 Mutation Responsive to Deep Brain Stimulation.
|
26060304 |
2016 |
rs886039494
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Clinical Course of Six Children With GNAO1 Mutations Causing a Severe and Distinctive Movement Disorder.
|
27068059 |
2016 |
rs886039494
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Phenotypic spectrum of GNAO1 variants: epileptic encephalopathy to involuntary movements with severe developmental delay.
|
25966631 |
2016 |
rs886039494
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Progressive Movement Disorder in Brothers Carrying a GNAO1 Mutation Responsive to Deep Brain Stimulation.
|
26060304 |
2016 |
rs797044951
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios.
|
25590979 |
2015 |
rs797044951
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Clinical whole-exome sequencing reveals a novel missense pathogenic variant of GNAO1 in a patient with infantile-onset epilepsy.
|
26485252 |
2015 |
rs886039494
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios.
|
25590979 |
2015 |
rs886039494
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Clinical whole-exome sequencing reveals a novel missense pathogenic variant of GNAO1 in a patient with infantile-onset epilepsy.
|
26485252 |
2015 |
rs797044951
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
De Novo mutations in GNAO1, encoding a Gαo subunit of heterotrimeric G proteins, cause epileptic encephalopathy.
|
23993195 |
2013 |
rs886039494
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
De Novo mutations in GNAO1, encoding a Gαo subunit of heterotrimeric G proteins, cause epileptic encephalopathy.
|
23993195 |
2013 |
rs797044951
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Augmented glucose-induced insulin release in mice lacking G(o2), but not G(o1) or G(i) proteins.
|
21220323 |
2011 |
rs886039494
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Augmented glucose-induced insulin release in mice lacking G(o2), but not G(o1) or G(i) proteins.
|
21220323 |
2011 |
rs797044951
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
G alpha(o) is necessary for muscarinic regulation of Ca2+ channels in mouse heart.
|
9050846 |
1997 |
rs886039494
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
G alpha(o) is necessary for muscarinic regulation of Ca2+ channels in mouse heart.
|
9050846 |
1997 |
rs886039494
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|