rs121912656
|
|
Li-Fraumeni Syndrome
|
T |
0.800 |
CausalMutation
|
CLINVAR |
The p53-reactivating small molecule RITA induces senescence in head and neck cancer cells.
|
25119136 |
2014 |
rs121912656
|
|
Li-Fraumeni Syndrome
|
T |
0.800 |
CausalMutation
|
CLINVAR |
Two hot spot mutant p53 mouse models display differential gain of function in tumorigenesis.
|
23538418 |
2013 |
rs121912656
|
|
Li-Fraumeni Syndrome
|
T |
0.800 |
CausalMutation
|
CLINVAR |
TP53 mutations and polymorphisms in primary myelofibrosis.
|
22052707 |
2012 |
rs121912656
|
|
Li-Fraumeni Syndrome
|
T |
0.800 |
CausalMutation
|
CLINVAR |
A comprehensive study of TP53 mutations in chronic lymphocytic leukemia: Analysis of 1287 diagnostic and 1148 follow-up CLL samples.
|
21232794 |
2011 |
rs121912656
|
|
Li-Fraumeni Syndrome
|
T |
0.800 |
CausalMutation
|
CLINVAR |
Analysis of the DNA-binding activity of p53 mutants using functional protein microarrays and its relationship to transcriptional activation.
|
20128691 |
2010 |
rs121912656
|
|
Li-Fraumeni Syndrome
|
T |
0.800 |
CausalMutation
|
CLINVAR |
Transcriptional functionality of germ line p53 mutants influences cancer phenotype.
|
17606709 |
2007 |
rs121912656
|
|
Li-Fraumeni Syndrome
|
T |
0.800 |
CausalMutation
|
CLINVAR |
A Li-Fraumeni syndrome family with retained heterozygosity for a germline TP53 mutation in two tumors.
|
12885464 |
2003 |
rs121912656
|
|
Li-Fraumeni Syndrome
|
T |
0.800 |
CausalMutation
|
CLINVAR |
Understanding the function-structure and function-mutation relationships of p53 tumor suppressor protein by high-resolution missense mutation analysis.
|
12826609 |
2003 |
rs121912656
|
|
Li-Fraumeni Syndrome
|
T |
0.800 |
CausalMutation
|
CLINVAR |
Heterogeneity in Li-Fraumeni families: p53 mutation analysis and immunohistochemical staining.
|
7783166 |
1995 |
rs121912656
|
|
Li-Fraumeni Syndrome
|
T |
0.800 |
CausalMutation
|
CLINVAR |
Screening for germ line TP53 mutations in breast cancer patients.
|
1591732 |
1992 |
rs121912656
|
|
Li-Fraumeni Syndrome
|
T |
0.800 |
CausalMutation
|
CLINVAR |
Prevalence and spectrum of germline mutations of the p53 gene among patients with sarcoma.
|
1565143 |
1992 |
rs121912656
|
|
Li-Fraumeni Syndrome
|
T |
0.800 |
CausalMutation
|
CLINVAR |
Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome.
|
2259385 |
1991 |
rs121912656
|
|
Li-Fraumeni Syndrome
|
A |
0.800 |
GeneticVariation
|
CLINVAR |
|
|
|
rs121912656
|
|
Liver carcinoma
|
G |
0.710 |
GeneticVariation
|
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs121912656
|
|
Glioblastoma
|
T |
0.710 |
GeneticVariation
|
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs121912656
|
|
Glioblastoma
|
G |
0.710 |
GeneticVariation
|
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs121912656
|
|
Liver carcinoma
|
A |
0.710 |
GeneticVariation
|
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs121912656
|
|
Squamous cell carcinoma of the head and neck
|
G |
0.710 |
GeneticVariation
|
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs121912656
|
|
Liver carcinoma
|
T |
0.710 |
GeneticVariation
|
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs121912656
|
|
Squamous cell carcinoma of the head and neck
|
T |
0.710 |
GeneticVariation
|
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs121912656
|
|
Glioblastoma
|
A |
0.710 |
GeneticVariation
|
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs121912656
|
|
Squamous cell carcinoma of the head and neck
|
A |
0.710 |
GeneticVariation
|
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs121912656
|
|
Uterine Carcinosarcoma
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs121912656
|
|
Brain Neoplasms
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |
rs121912656
|
|
Squamous cell carcinoma of lung
|
A |
0.700 |
GeneticVariation
|
CLINVAR |
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
|
26619011 |
2016 |