rs868137297
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Germline mutations in 40 cancer susceptibility genes among Chinese patients with high hereditary risk breast cancer.
|
29752822 |
2019 |
rs1057519992
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mutational processes shape the landscape of TP53 mutations in human cancer.
|
30224644 |
2018 |
rs1057520007
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Clinical characteristics and registry-validated extended pedigrees of germline TP53 mutation carriers in Denmark.
|
29324801 |
2018 |
rs1064795203
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mutational processes shape the landscape of TP53 mutations in human cancer.
|
30224644 |
2018 |
rs11575996
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Clinical characteristics and registry-validated extended pedigrees of germline TP53 mutation carriers in Denmark.
|
29324801 |
2018 |
rs786202962
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Contribution of de novo and mosaic TP53 mutations to Li-Fraumeni syndrome.
|
29070607 |
2018 |
rs876660821
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mutational processes shape the landscape of TP53 mutations in human cancer.
|
30224644 |
2018 |
rs1064795203
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
The frequency of cancer predisposition gene mutations in hereditary breast and ovarian cancer patients in Taiwan: From BRCA1/2 to multi-gene panels.
|
28961279 |
2017 |
rs121912655
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
The Clinical Utility of Next Generation Sequencing Results in a Community-Based Hereditary Cancer Risk Program.
|
27276934 |
2017 |
rs121913344
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Li-Fraumeni syndrome presenting as mucosal melanoma: Case report and treatment considerations.
|
27726232 |
2017 |
rs267605076
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Synonymous mutation in TP53 results in a cryptic splice site affecting its DNA-binding site in an adolescent with two primary sarcomas.
|
28475293 |
2017 |
rs730882018
|
|
CG |
0.700 |
CausalMutation |
CLINVAR |
Germline TP53 mutations result into a constitutive defect of p53 DNA binding and transcriptional response to DNA damage.
|
28369373 |
2017 |
rs876660821
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Germline Mutations in Cancer Susceptibility Genes in a Large Series of Unselected Breast Cancer Patients.
|
28724667 |
2017 |
rs1057519989
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Genetic and functional analysis of a Li Fraumeni syndrome family in China.
|
26818906 |
2016 |
rs1131691026
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
TP53 Variations in Human Cancers: New Lessons from the IARC TP53 Database and Genomics Data.
|
27328919 |
2016 |
rs1131691026
|
|
T |
0.700 |
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 |
rs11575997
|
|
T |
0.700 |
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 |
rs17882252
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Inherited mutations in cancer susceptibility genes are common among survivors of breast cancer who develop therapy-related leukemia.
|
26641009 |
2016 |
rs397516434
|
|
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 |
rs397516434
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Risks of first and subsequent cancers among TP53 mutation carriers in the National Cancer Institute Li-Fraumeni syndrome cohort.
|
27496084 |
2016 |
rs397516435
|
|
A |
0.700 |
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 |
rs397516435
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol.
|
26787237 |
2016 |
rs55863639
|
|
T |
0.700 |
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 |
rs587780074
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Targeted massively parallel sequencing of a panel of putative breast cancer susceptibility genes in a large cohort of multiple-case breast and ovarian cancer families.
|
26534844 |
2016 |
rs730882001
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |