Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587782705
rs587782705
TP53
0.800 GeneticVariation UNIPROT Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. 27854360

2017
dbSNP: rs587782705
rs587782705
TP53
0.800 GeneticVariation UNIPROT A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. 25394175

2015
dbSNP: rs587782705
rs587782705
TP53
A 0.800 CausalMutation CLINVAR Prevalence and functional consequence of TP53 mutations in pediatric adrenocortical carcinoma: a children's oncology group study. 25584008

2015
dbSNP: rs587782705
rs587782705
TP53
A 0.800 CausalMutation CLINVAR Germline TP53 Mutations in Patients With Early-Onset Colorectal Cancer in the Colon Cancer Family Registry. 26086041

2015
dbSNP: rs587782705
rs587782705
TP53
0.800 GeneticVariation UNIPROT ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing. 25356965

2015
dbSNP: rs587782705
rs587782705
TP53
0.800 GeneticVariation UNIPROT American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers. 24493721

2014
dbSNP: rs587782705
rs587782705
TP53
0.800 GeneticVariation UNIPROT ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. 23788249

2013
dbSNP: rs587782705
rs587782705
TP53
A 0.800 CausalMutation CLINVAR Dominant-negative features of mutant TP53 in germline carriers have limited impact on cancer outcomes. 21343334

2011
dbSNP: rs587782705
rs587782705
TP53
A 0.800 CausalMutation CLINVAR Gastric cancer in individuals with Li-Fraumeni syndrome. 21552135

2011
dbSNP: rs587782705
rs587782705
TP53
A 0.800 CausalMutation CLINVAR Familial pediatric endocrine tumors. 21934104

2011
dbSNP: rs587782705
rs587782705
TP53
0.800 GeneticVariation UNIPROT American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility. 20065170

2010
dbSNP: rs587782705
rs587782705
TP53
A 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
dbSNP: rs587782705
rs587782705
TP53
A 0.800 CausalMutation CLINVAR Predicting positive p53 cancer rescue regions using Most Informative Positive (MIP) active learning. 19756158

2009
dbSNP: rs587782705
rs587782705
TP53
A 0.800 CausalMutation CLINVAR Molecular basis of the Li-Fraumeni syndrome: an update from the French LFS families. 18511570

2008
dbSNP: rs587782705
rs587782705
TP53
A 0.800 CausalMutation CLINVAR Younger age of cancer initiation is associated with shorter telomere length in Li-Fraumeni syndrome. 17308077

2007
dbSNP: rs587782705
rs587782705
TP53
A 0.800 CausalMutation CLINVAR Transcriptional functionality of germ line p53 mutants influences cancer phenotype. 17606709

2007
dbSNP: rs587782705
rs587782705
TP53
A 0.800 CausalMutation CLINVAR The TP53 mutation, R337H, is associated with Li-Fraumeni and Li-Fraumeni-like syndromes in Brazilian families. 16494995

2007
dbSNP: rs587782705
rs587782705
TP53
0.800 GeneticVariation UNIPROT American Cancer Society guidelines for breast screening with MRI as an adjunct to mammography. 17392385

2007
dbSNP: rs587782705
rs587782705
TP53
A 0.800 CausalMutation CLINVAR Successful treatment of an unresectable choroid plexus carcinoma in a patient with Li-Fraumeni syndrome. 15654279

2005
dbSNP: rs587782705
rs587782705
TP53
0.800 GeneticVariation UNIPROT Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors. 15604628

2004
dbSNP: rs587782705
rs587782705
TP53
A 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
dbSNP: rs587782705
rs587782705
TP53
0.800 GeneticVariation UNIPROT American Society of Clinical Oncology policy statement update: genetic testing for cancer susceptibility. 12692171

2003
dbSNP: rs587782705
rs587782705
TP53
A 0.800 CausalMutation CLINVAR Reactive oxygen species generated by PAH o-quinones cause change-in-function mutations in p53. 12067251

2002
dbSNP: rs587782705
rs587782705
TP53
A 0.800 CausalMutation CLINVAR Are there low-penetrance TP53 Alleles? evidence from childhood adrenocortical tumors. 10486318

1999
dbSNP: rs587782705
rs587782705
TP53
0.800 GeneticVariation UNIPROT Hereditary TP53 codon 292 and somatic P16INK4A codon 94 mutations in a Li-Fraumeni syndrome family. 10484981

1999