rs121918465
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs121918465
|
|
C |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs121918465
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia.
|
12717436 |
2003 |
rs121918465
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia.
|
12717436 |
2003 |
rs121918465
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
PTPN11 mutations in pediatric patients with acute myeloid leukemia: results from the Children's Cancer Group.
|
15385933 |
2004 |
rs121918465
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
Mutations in PTPN11 implicate the SHP-2 phosphatase in leukemogenesis.
|
14644997 |
2004 |
rs121918465
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
Genetic evidence for lineage-related and differentiation stage-related contribution of somatic PTPN11 mutations to leukemogenesis in childhood acute leukemia.
|
14982869 |
2004 |
rs121918465
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease.
|
15928039 |
2005 |
rs121918465
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease.
|
16358218 |
2006 |
rs121918465
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
Mutations of the PTPN11 and RAS genes in rhabdomyosarcoma and pediatric hematological malignancies.
|
16518851 |
2006 |
rs121918465
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
Structural and functional effects of disease-causing amino acid substitutions affecting residues Ala72 and Glu76 of the protein tyrosine phosphatase SHP-2.
|
17177198 |
2007 |
rs121918465
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
Correlation of clinical features with the mutational status of GM-CSF signaling pathway-related genes in juvenile myelomonocytic leukemia.
|
19047918 |
2009 |
rs121918465
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
Functional evaluation of circulating hematopoietic progenitors in Noonan syndrome.
|
23756559 |
2013 |
rs121918465
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
Juvenile myelomonocytic leukaemia and Noonan syndrome.
|
25097206 |
2014 |
rs121918465
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
|
24493721 |
2014 |
rs121918465
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Determination of the catalytic activity of LEOPARD syndrome-associated SHP2 mutants toward parafibromin, a bona fide SHP2 substrate involved in Wnt signaling.
|
26742426 |
2016 |