rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
T |
0.800 |
CausalMutation |
CLINVAR |
Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy.
|
21703448 |
2011 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
T |
0.800 |
CausalMutation |
CLINVAR |
Genotype-phenotype associations in SCN1A-related epilepsies.
|
21248271 |
2011 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
T |
0.800 |
CausalMutation |
CLINVAR |
Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome.
|
20431604 |
2010 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
T |
0.800 |
CausalMutation |
CLINVAR |
Targeted next generation sequencing as a diagnostic tool in epileptic disorders.
|
22612257 |
2012 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
T |
0.800 |
CausalMutation |
CLINVAR |
Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.
|
17561957 |
2007 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
T |
0.800 |
CausalMutation |
CLINVAR |
"Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of ""de novo"" SCN1A Mutations in Children with Dravet Syndrome."
|
26096185 |
2015 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
T |
0.800 |
CausalMutation |
CLINVAR |
Early clinical features and diagnosis of Dravet syndrome in 138 Chinese patients with SCN1A mutations.
|
24168886 |
2014 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
T |
0.800 |
CausalMutation |
CLINVAR |
De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy.
|
12754708 |
2003 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
T |
0.800 |
CausalMutation |
CLINVAR |
Dravet syndrome: seizure control and gait in adults with different SCN1A mutations.
|
22780858 |
2012 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
T |
0.800 |
CausalMutation |
CLINVAR |
Nonfunctional SCN1A is common in severe myoclonic epilepsy of infancy.
|
17054685 |
2006 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
T |
0.800 |
CausalMutation |
CLINVAR |
Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy.
|
23195492 |
2012 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
|
0.800 |
GeneticVariation |
UNIPROT |
EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementias.
|
20298421 |
2010 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
|
0.800 |
GeneticVariation |
UNIPROT |
Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome.
|
20431604 |
2010 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
|
0.800 |
GeneticVariation |
UNIPROT |
Genotype-phenotype correlations in a group of 15 SCN1A-mutated Italian patients with GEFS+ spectrum (seizures plus, classical and borderline severe myoclonic epilepsy of infancy).
|
20729507 |
2010 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome.
|
20522430 |
2010 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
|
0.800 |
GeneticVariation |
UNIPROT |
The spectrum of SCN1A-related infantile epileptic encephalopathies.
|
17347258 |
2007 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
|
0.800 |
GeneticVariation |
UNIPROT |
Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis.
|
26993267 |
2016 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
|
0.800 |
GeneticVariation |
UNIPROT |
De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy.
|
12754708 |
2003 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures.
|
12566275 |
2003 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
|
0.800 |
GeneticVariation |
UNIPROT |
Acute encephalopathy in children with Dravet syndrome.
|
22092154 |
2012 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
|
0.800 |
GeneticVariation |
UNIPROT |
Novel SCN1A mutations in Indonesian patients with severe myoclonic epilepsy in infancy.
|
19563458 |
2010 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
|
0.800 |
GeneticVariation |
UNIPROT |
Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy.
|
23195492 |
2012 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies.
|
19522081 |
2009 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
|
0.800 |
GeneticVariation |
UNIPROT |
Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy.
|
23662938 |
2013 |
rs121917927
|
SCN1A;SCN1A-AS1
|
Early Infantile Epileptic Encephalopathy 6
|
|
0.800 |
GeneticVariation |
UNIPROT |
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy.
|
12821740 |
2003 |