rs1060499616
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
|
|
|
rs1060502579
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1555889984
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1555899813
|
|
TCC |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1569084116
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1569084530
|
|
GCGCCGGCGTCCGGGGCGCCCAGCGGCAA |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs267607026
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs587776809
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555889984
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
A novel germline RUNX1 mutation with co-occurrence of somatic alterations in a case of myeloid neoplasm with familial thrombocytopenia: first report from India.
|
30990344 |
2019 |
rs74315451
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
A novel inherited mutation of the transcription factor RUNX1 causes thrombocytopenia and may predispose to acute myeloid leukaemia.
|
12060124 |
2002 |
rs1057519748
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
A novel pedigree with heterozygous germline RUNX1 mutation causing familial MDS-related AML: can these families serve as a multistep model for leukemic transformation?
|
19387465 |
2009 |
rs1060499616
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Analyses of Genetic and Clinical Parameters for Screening Patients With Inherited Thrombocytopenia with Small or Normal-Sized Platelets.
|
26175287 |
2015 |
rs587776809
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Analyses of Genetic and Clinical Parameters for Screening Patients With Inherited Thrombocytopenia with Small or Normal-Sized Platelets.
|
26175287 |
2015 |
rs74315450
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Application of whole-exome sequencing to direct the specific functional testing and diagnosis of rare inherited bleeding disorders in patients from the Öresund Region, Scandinavia.
|
28748566 |
2017 |
rs1060499616
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Biological Activities of RUNX1 Mutants Predict Secondary Acute Leukemia Transformation from Chronic Myelomonocytic Leukemia and Myelodysplastic Syndromes.
|
25840971 |
2015 |
rs74315450
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Biological Activities of RUNX1 Mutants Predict Secondary Acute Leukemia Transformation from Chronic Myelomonocytic Leukemia and Myelodysplastic Syndromes.
|
25840971 |
2015 |
rs1555899735
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Biological Activities of RUNX1 Mutants Predict Secondary Acute Leukemia Transformation from Chronic Myelomonocytic Leukemia and Myelodysplastic Syndromes.
|
25840971 |
2015 |
rs74315450
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant-negative, or hypomorphic alleles.
|
17290219 |
2007 |
rs121912498
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant-negative, or hypomorphic alleles.
|
17290219 |
2007 |
rs74315450
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Functional features of RUNX1 mutants in acute transformation of chronic myeloid leukemia and their contribution to inducing murine full-blown leukemia.
|
22318203 |
2012 |
rs74315450
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders.
|
27112265 |
2016 |
rs267607026
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders.
|
27112265 |
2016 |
rs587776811
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders.
|
27112265 |
2016 |
rs1060499616
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.
|
10508512 |
1999 |
rs1060499616
|
|
T |
0.800 |
GeneticVariation |
CLINVAR |
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.
|
10508512 |
1999 |