Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
0.810 GeneticVariation BEFREE We identified a missense germline mutation (Gly245Ser) in one of the mutation hot spots of the TP53 gene in two affected members of a Li-Fraumeni syndrome family. 12885464

2003

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
A 0.810 CausalMutation CLINVAR Li-Fraumeni and Li-Fraumeni-like syndrome among children diagnosed with pediatric cancer in Southern Brazil. 24122735

2013

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
T 0.810 CausalMutation CLINVAR Heterogeneity in Li-Fraumeni families: p53 mutation analysis and immunohistochemical staining. 7783166

1995

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
T 0.810 CausalMutation CLINVAR Dominant-negative features of mutant TP53 in germline carriers have limited impact on cancer outcomes. 21343334

2011

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
T 0.810 CausalMutation CLINVAR Prevalence and spectrum of germline mutations of the p53 gene among patients with sarcoma. 1565143

1992

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
T 0.810 CausalMutation CLINVAR Detection of 11 germline inactivating TP53 mutations and absence of TP63 and HCHK2 mutations in 17 French families with Li-Fraumeni or Li-Fraumeni-like syndrome. 11370630

2001

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
T 0.810 CausalMutation CLINVAR Successful treatment of a patient with Li-Fraumeni syndrome and metastatic lung adenocarcinoma harboring synchronous EGFR L858R and ERBB2 extracellular domain S310F mutations with the pan-HER inhibitor afatinib. 24835218

2014

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
T 0.810 CausalMutation CLINVAR Mutant p53 proteins bind DNA in a DNA structure-selective mode. 15722483

2005

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
T 0.810 CausalMutation CLINVAR Incidence of germ-line p53 mutations in patients with gliomas. 8550239

1995

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
T 0.810 CausalMutation CLINVAR Li-Fraumeni syndrome--a molecular and clinical review. 9218725

1997

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
A 0.810 CausalMutation CLINVAR Impact of mutant p53 functional properties on TP53 mutation patterns and tumor phenotype: lessons from recent developments in the IARC TP53 database. 17311302

2007

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
T 0.810 CausalMutation CLINVAR We identified a missense germline mutation (Gly245Ser) in one of the mutation hot spots of the TP53 gene in two affected members of a Li-Fraumeni syndrome family. 12885464

2003

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
A 0.810 CausalMutation CLINVAR Dominant-negative features of mutant TP53 in germline carriers have limited impact on cancer outcomes. 21343334

2011

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
T 0.810 CausalMutation CLINVAR Li-Fraumeni and Li-Fraumeni-like syndrome among children diagnosed with pediatric cancer in Southern Brazil. 24122735

2013

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
A 0.810 CausalMutation CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312

2016

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
A 0.810 CausalMutation CLINVAR Understanding the function-structure and function-mutation relationships of p53 tumor suppressor protein by high-resolution missense mutation analysis. 12826609

2003

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
T 0.810 CausalMutation CLINVAR p53 gene mutations in pediatric brain tumors. 7565304

1995

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
T 0.810 CausalMutation CLINVAR Screening for germ line TP53 mutations in breast cancer patients. 1591732

1992

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
T 0.810 CausalMutation CLINVAR Analysis of the DNA-binding activity of p53 mutants using functional protein microarrays and its relationship to transcriptional activation. 20128691

2010

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
A 0.810 CausalMutation CLINVAR Characterization of the p53 mutants ability to inhibit p73 beta transactivation using a yeast-based functional assay. 12917626

2003

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
T 0.810 CausalMutation CLINVAR Two hot spot mutant p53 mouse models display differential gain of function in tumorigenesis. 23538418

2013

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
A 0.810 CausalMutation CLINVAR Analysis of the DNA-binding activity of p53 mutants using functional protein microarrays and its relationship to transcriptional activation. 20128691

2010

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
T 0.810 CausalMutation CLINVAR Prevalence of early onset colorectal cancer in 397 patients with classic Li-Fraumeni syndrome. 16401470

2006

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
A 0.810 CausalMutation CLINVAR Establishment and characterization of the first pediatric adrenocortical carcinoma xenograft model identifies topotecan as a potential chemotherapeutic agent. 23406775

2013

dbSNP: rs28934575
rs28934575
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome
T 0.810 CausalMutation CLINVAR Germ-line mutations of TP53 in Li-Fraumeni families: an extended study of 39 families. 9242456

1997