rs1057519894
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Cutaneous Melanoma
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs1057519894
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Cutaneous Melanoma
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs1057519894
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Lymphoma, Non-Hodgkin, Familial
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs267601394
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Lymphoma, Non-Hodgkin, Familial
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs267601394
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Cutaneous Melanoma
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs267601394
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Cutaneous Melanoma
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs267601394
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Lymphoma, Non-Hodgkin, Familial
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs267601395
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Lymphoma, Non-Hodgkin, Familial
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs267601395
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Cutaneous Melanoma
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs267601395
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Cutaneous Melanoma
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs267601395
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Lymphoma, Non-Hodgkin, Familial
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs397515547
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Weaver syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
Weaver Syndrome-Associated EZH2 Protein Variants Show Impaired Histone Methyltransferase Function In Vitro.
|
26694085 |
2016 |
rs397515548
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Weaver syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
Weaver Syndrome-Associated EZH2 Protein Variants Show Impaired Histone Methyltransferase Function In Vitro.
|
26694085 |
2016 |
rs775407864
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Weaver syndrome
|
G |
0.700 |
CausalMutation |
CLINVAR |
Use of Targeted Exome Sequencing for Molecular Diagnosis of Skeletal Disorders.
|
26380986 |
2015 |
rs1554499814
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Dysmorphic features
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype.
|
24214728 |
2013 |
rs1554499814
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Overgrowth
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype.
|
24214728 |
2013 |
rs397515547
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Weaver syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
Weaver syndrome and defective cortical development: a rare association.
|
23239504 |
2013 |
rs397515548
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Weaver syndrome
|
|
0.700 |
GeneticVariation |
UNIPROT |
Weaver syndrome and defective cortical development: a rare association.
|
23239504 |
2013 |
rs797044844
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Weaver syndrome
|
C |
0.700 |
CausalMutation |
CLINVAR |
Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype.
|
24214728 |
2013 |
rs1554499814
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Overgrowth
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Mutations in EZH2 cause Weaver syndrome.
|
22177091 |
2012 |
rs1554499814
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Dysmorphic features
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Mutations in EZH2 cause Weaver syndrome.
|
22177091 |
2012 |
rs1554499814
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Dysmorphic features
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Evolution and functional impact of rare coding variation from deep sequencing of human exomes.
|
22604720 |
2012 |
rs1554499814
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Overgrowth
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Evolution and functional impact of rare coding variation from deep sequencing of human exomes.
|
22604720 |
2012 |
rs267601395
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Lymphoma
|
G |
0.700 |
GeneticVariation |
CLINVAR |
A selective inhibitor of EZH2 blocks H3K27 methylation and kills mutant lymphoma cells.
|
23023262 |
2012 |
rs267601395
|
Entrez Id: |
2146 |
Gene Symbol: |
EZH2 |
EZH2
|
Lymphoma
|
T |
0.700 |
GeneticVariation |
CLINVAR |
A selective inhibitor of EZH2 blocks H3K27 methylation and kills mutant lymphoma cells.
|
23023262 |
2012 |