×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
GeneticVariation
CLINVAR
A boy with Burkitt lymphoma associated with Noonan syndrome due to a mutation in RAF1.
23613113
2013
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
CausalMutation
CLINVAR
A boy with Burkitt lymphoma associated with Noonan syndrome due to a mutation in RAF1.
23613113
2013
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
GeneticVariation
CLINVAR
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.
17603483
2007
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
CausalMutation
CLINVAR
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.
17603483
2007
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
CausalMutation
CLINVAR
Germline gain-of-function mutations in RAF1 cause Noonan syndrome.
17603482
2007
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
GeneticVariation
CLINVAR
Germline gain-of-function mutations in RAF1 cause Noonan syndrome.
17603482
2007
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
GeneticVariation
CLINVAR
Growth patterns of patients with Noonan syndrome: correlation with age and genotype.
26903553
2016
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
CausalMutation
CLINVAR
Growth patterns of patients with Noonan syndrome: correlation with age and genotype.
26903553
2016
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
GeneticVariation
CLINVAR
Increased BRAF heterodimerization is the common pathogenic mechanism for noonan syndrome-associated RAF1 mutants.
22826437
2012
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
CausalMutation
CLINVAR
Increased BRAF heterodimerization is the common pathogenic mechanism for noonan syndrome-associated RAF1 mutants.
22826437
2012
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
CausalMutation
CLINVAR
LEOPARD syndrome: clinical diagnosis in the first year of life.
16523510
2006
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
GeneticVariation
CLINVAR
LEOPARD syndrome: clinical diagnosis in the first year of life.
16523510
2006
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
CausalMutation
CLINVAR
Molecular and clinical analysis of RAF1 in Noonan syndrome and related disorders: dephosphorylation of serine 259 as the essential mechanism for mutant activation.
20052757
2010
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
GeneticVariation
CLINVAR
Molecular and clinical analysis of RAF1 in Noonan syndrome and related disorders: dephosphorylation of serine 259 as the essential mechanism for mutant activation.
20052757
2010
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
GeneticVariation
CLINVAR
Noonan syndrome and clinically related disorders.
21396583
2011
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
CausalMutation
CLINVAR
Noonan syndrome and clinically related disorders.
21396583
2011
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
GeneticVariation
CLINVAR
Noonan syndrome: clinical features, diagnosis, and management guidelines.
20876176
2010
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
CausalMutation
CLINVAR
Noonan syndrome: clinical features, diagnosis, and management guidelines.
20876176
2010
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
GeneticVariation
CLINVAR
Noonan syndrome: crossed fused ectopic kidneys and focal segmental glomerulosclerosis-a rare association.
19437094
2009
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
CausalMutation
CLINVAR
Noonan syndrome: crossed fused ectopic kidneys and focal segmental glomerulosclerosis-a rare association.
19437094
2009
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
GeneticVariation
CLINVAR
RAF1 mutations in childhood-onset dilated cardiomyopathy.
24777450
2014
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
CausalMutation
CLINVAR
RAF1 mutations in childhood-onset dilated cardiomyopathy.
24777450
2014
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
CausalMutation
CLINVAR
Recent advances in RASopathies.
26446362
2016
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
GeneticVariation
CLINVAR
Recent advances in RASopathies.
26446362
2016
×
Entrez Id:
5894
Gene Symbol:
RAF1
RAF1
Dysmorphic features
0.100
GeneticVariation
CLINVAR
Spectrum of mutations in Noonan syndrome and their correlation with phenotypes.
21784453
2011