rs587780070
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Gestational choriocarcinoma associated with a germline TP53 mutation.
|
28477316 |
2018 |
rs587780070
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Germline TP53 mutations result into a constitutive defect of p53 DNA binding and transcriptional response to DNA damage.
|
28369373 |
2017 |
rs121912664
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Tetramer formation of tumor suppressor protein p53: Structure, function, and applications.
|
26572807 |
2016 |
rs121912664
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Early-onset breast cancer patients in the South and Southeast of Brazil should be tested for the TP53 p.R337H mutation.
|
27223487 |
2016 |
rs121912664
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
The Inherited p53 Mutation in the Brazilian Population.
|
27663983 |
2016 |
rs28934574
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Detection of high frequency of mutations in a breast and/or ovarian cancer cohort: implications of embracing a multi-gene panel in molecular diagnosis in India.
|
26911350 |
2016 |
rs28934574
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Gain of function of mutant p53: R282W on the peak?
|
26878390 |
2016 |
rs28934575
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Panel Testing for Familial Breast Cancer: Calibrating the Tension Between Research and Clinical Care.
|
26786923 |
2016 |
rs28934576
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Germline TP53 Mutation and Clinical Characteristics of Korean Patients With Li-Fraumeni Syndrome.
|
27374712 |
2016 |
rs587782144
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: 11 year follow-up of a prospective observational study.
|
27501770 |
2016 |
rs786201057
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Improving performance of multigene panels for genomic analysis of cancer predisposition.
|
26845104 |
2016 |
rs121912664
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
R337H mutation of the TP53 gene as a clinical marker in cancer patients: a systematic review of literature.
|
26681051 |
2015 |
rs121912664
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Occurrence of Neuroblastoma among TP53 p.R337H Carriers.
|
26452166 |
2015 |
rs28934574
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Candidate gene analysis of BRCA1/2 mutation-negative high-risk Russian breast cancer patients.
|
25619955 |
2015 |
rs28934574
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers.
|
26014290 |
2015 |
rs28934576
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
A child with Li-Fraumeni syndrome: Modes to inactivate the second allele of TP53 in three different malignancies.
|
25787918 |
2015 |
rs397514495
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Clinical Application of Multigene Panels: Challenges of Next-Generation Counseling and Cancer Risk Management.
|
26484312 |
2015 |
rs397514495
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel.
|
25186627 |
2015 |
rs587780070
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
EFGR-mutant lung adenocarcinoma and Li-Fraumeni syndrome: report of two cases and review of the literature.
|
25433984 |
2015 |
rs587780070
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers.
|
26014290 |
2015 |
rs587782144
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers.
|
26014290 |
2015 |
rs786201057
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers.
|
26014290 |
2015 |
rs786201057
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Prevalence of mutations in a panel of breast cancer susceptibility genes in BRCA1/2-negative patients with early-onset breast cancer.
|
25503501 |
2015 |
rs879253894
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Germline TP53 mutational spectrum in French Canadians with breast cancer.
|
25925845 |
2015 |
rs879253894
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Prevalence and functional consequence of TP53 mutations in pediatric adrenocortical carcinoma: a children's oncology group study.
|
25584008 |
2015 |