rs147001633
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs147001633
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs147001633
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
AML cells with the R882H mutation have severely reduced de novo methyltransferase activity and focal hypomethylation at specific CpGs throughout AML cell genomes.
|
24656771 |
2014 |
rs147001633
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Molecular evaluation of DNMT3A and IDH1/2 gene mutation: frequency, distribution pattern and associations with additional molecular markers in normal karyotype Indian acute myeloid leukemia patients.
|
24606448 |
2014 |
rs147001633
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Cancer stem cells: Tracing clones.
|
22898540 |
2012 |
rs147001633
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
Retroviral oncogenes: a historical primer.
|
22898541 |
2012 |
rs147001633
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
The role of mutations in epigenetic regulators in myeloid malignancies.
|
22898539 |
2012 |
rs147001633
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Three heterozygous mutations (p.R882S, p.R882C and p.R882H) were identified in three of 61 AML patients, whereas none of patients with other hematological disorders harbored any mutation.
|
22744846 |
2012 |
rs147001633
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Impact of genetic features on treatment decisions in AML.
|
22160010 |
2011 |
rs147001633
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
Impact of genetic features on treatment decisions in AML.
|
22160010 |
2011 |
rs147001633
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
[Analysis of DNMT3a gene mutations in acute myelogenous leukemia].
|
21518476 |
2011 |
rs147001633
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
Impact of genetic features on treatment decisions in AML.
|
22160010 |
2011 |
rs147001633
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
DNMT3A mutations in acute myeloid leukemia.
|
21067377 |
2010 |
rs147001633
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
DNMT3A mutations in acute myeloid leukemia.
|
21067377 |
2010 |
rs377577594
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs377577594
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
Molecular evaluation of DNMT3A and IDH1/2 gene mutation: frequency, distribution pattern and associations with additional molecular markers in normal karyotype Indian acute myeloid leukemia patients.
|
24606448 |
2014 |
rs377577594
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
Three heterozygous mutations (p.R882S, p.R882C and p.R882H) were identified in three of 61 AML patients, whereas none of patients with other hematological disorders harbored any mutation.
|
22744846 |
2012 |
rs377577594
|
|
C |
0.710 |
CausalMutation |
CLINVAR |
The role of mutations in epigenetic regulators in myeloid malignancies.
|
22898539 |
2012 |
rs377577594
|
|
T |
0.710 |
CausalMutation |
CLINVAR |
Cancer stem cells: Tracing clones.
|
22898540 |
2012 |
rs377577594
|
|
T |
0.710 |
CausalMutation |
CLINVAR |
Three heterozygous mutations (p.R882S, p.R882C and p.R882H) were identified in three of 61 AML patients, whereas none of patients with other hematological disorders harbored any mutation.
|
22744846 |
2012 |
rs377577594
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
The role of mutations in epigenetic regulators in myeloid malignancies.
|
22898539 |
2012 |
rs377577594
|
|
T |
0.710 |
CausalMutation |
CLINVAR |
Impact of genetic features on treatment decisions in AML.
|
22160010 |
2011 |
rs377577594
|
|
T |
0.710 |
CausalMutation |
CLINVAR |
[Analysis of DNMT3a gene mutations in acute myelogenous leukemia].
|
21518476 |
2011 |
rs377577594
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
[Analysis of DNMT3a gene mutations in acute myelogenous leukemia].
|
21518476 |
2011 |
rs377577594
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
Impact of genetic features on treatment decisions in AML.
|
22160010 |
2011 |