×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
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
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
CausalMutation
CLINVAR
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer.
27153395
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
CausalMutation
CLINVAR
Inherited breast cancer predisposition in Asians: multigene panel testing outcomes from Singapore.
29263802
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
CausalMutation
CLINVAR
Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors.
26822237
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
GeneticVariation
CLINVAR
Assessing mutant p53 in primary high-grade serous ovarian cancer using immunohistochemistry and massively parallel sequencing.
27189670
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
GeneticVariation
CLINVAR
Heterozygous p53(V172F) mutation in cisplatin-resistant human tumor cells promotes MDM4 recruitment and decreases stability and transactivity of p53.
26876197
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
GeneticVariation
CLINVAR
Modeling the Etiology of p53-mutated Cancer Cells.
27022024
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
CausalMutation
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
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
GeneticVariation
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
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
GeneticVariation
CLINVAR
Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol.
26787237
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
GeneticVariation
CLINVAR
Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors.
26822237
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
CausalMutation
CLINVAR
Panel Testing for Familial Breast Cancer: Calibrating the Tension Between Research and Clinical Care.
26786923
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
CausalMutation
CLINVAR
Implementation of next-generation sequencing for molecular diagnosis of hereditary breast and ovarian cancer highlights its genetic heterogeneity.
27553368
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
CausalMutation
CLINVAR
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
26681312
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
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
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
CausalMutation
CLINVAR
TP53 gene mutation analysis in chronic lymphocytic leukemia by nanopore MinION sequencing.
27724982
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
GeneticVariation
CLINVAR
Genetic and functional analysis of a Li Fraumeni syndrome family in China.
26818906
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
CausalMutation
CLINVAR
Germline TP53 Mutation and Clinical Characteristics of Korean Patients With Li-Fraumeni Syndrome.
27374712
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
CausalMutation
CLINVAR
Incidentalome from Genomic Sequencing: A Barrier to Personalized Medicine?
27077130
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
CausalMutation
CLINVAR
Clinical significance of frequent somatic mutations detected by high-throughput targeted sequencing in archived colorectal cancer samples.
27146902
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
GeneticVariation
CLINVAR
Clinical significance of frequent somatic mutations detected by high-throughput targeted sequencing in archived colorectal cancer samples.
27146902
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
GeneticVariation
CLINVAR
Mutation analysis of 13 driver genes of colorectal cancer-related pathways in Taiwanese patients.
26900293
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
CausalMutation
CLINVAR
Rare germline variant (rs78378222) in the TP53 3' UTR: Evidence for a new mechanism of cancer predisposition in Li-Fraumeni syndrome.
26823150
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
GeneticVariation
CLINVAR
Complex analysis of the p53 tumor suppressor in lung carcinoma.
26718964
2016
×
Entrez Id:
7157
Gene Symbol:
TP53
TP53
Neoplastic Syndromes, Hereditary
0.170
GeneticVariation
CLINVAR
Lenalidomide normalizes tumor vessels in colorectal cancer improving chemotherapy activity.
27149858
2016