Varaico: Literature-Extracted Genetic Variants

Gene:TP53
Variant:p.S240T
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TP53

NM_000546.6:p.S240T

Associated Papers

TP53 Functional-Domain-Specific Mutations Define Distinct Clinical Outcomes in EGFR-Mutant Non-Small Cell Lung Cancer Treated with EGFR Tyrosine Kinase Inhibitors.

Kobayashi K

Journal of Clinical Medicine, 2026

41753239 (PubMed )
Supplement: jcm-15-01552-s001.zip › jcm-4078632-supplementary.pdf

TP53 mutation heterogeneity reveals distinct prognoses in mantle cell lymphoma.

Liu S et al.

Annals of Hematology, 2026

41559357 (PubMed )
Supplement: 277_2026_6771_MOESM2_ESM.xlsx › TableS3

Deep CRISPR mutagenesis characterizes the functional diversity of TP53 mutations.

Funk JS et al.

Nature Genetics, 2025

39774325 (PubMed )
Supplement: 41588_2024_2039_MOESM5_ESM.xlsx › SuppFig6

The Advantage of Targeted Next-Generation Sequencing over qPCR in Testing for Druggable EGFR Variants in Non-Small-Cell Lung Cancer.

Szpechcinski A et al.

International Journal of Molecular Sciences, 2024

39063150 (PubMed )
Supplement: ijms-25-07908-s001.zip › ijms-3103240-supplementary.pdf

Activity of osimeRTInib in non-small-cell lung Cancer with UNcommon epidermal growth factor receptor mutations: retrospective Observational multicenter study (ARTICUNO).

Pizzutilo EG et al.

Esmo Open, 2024

38878323 (PubMed )
Supplement: mmc1.docx

Mutations in the TP53, VEGFA, and CTH Genes as Key Molecular Markers for the Diagnosis of Glioblastoma.

Khalil SS et al.

Cureus, 2024

Assessments of TP53 and CTNNB1 gene hotspot mutations in circulating tumour DNA of hepatitis B virus-induced hepatocellular carcinoma.

Kumar S et al.

Frontiers in Genetics, 2023

Case report: olaparib use in metastatic lung adenocarcinoma with BRCA2 pathogenic variant.

Soon Jian Hao J et al.

Cold Spring Harbor Molecular Case Studies, 2022

36577523 (PubMed )
Supplement: supp_mcs.a006223_Supplemental_Material.pdf

Landscape of EGFR mutations in lung adenocarcinoma: a single institute experience with comparison of PANAMutyper testing and targeted next-generation sequencing.

Lee J et al.

Journal of Pathology and Translational Medicine, 2022

Dacomitinib for Advanced Non-small Cell Lung Cancer Patients Harboring Major Uncommon EGFR Alterations: A Dual-Center, Single-Arm, Ambispective Cohort Study in China.

Li HS et al.

Frontiers in Pharmacology, 2022

Comprehensive analyses of genomic features and mutational signatures in adenosquamous carcinoma of the lung.

Wang H et al.

Frontiers in Oncology, 2022

Analysis of single-nucleotide polymorphisms in genes associated with triple-negative breast cancer.

G V et al.

Frontiers in Genetics, 2022

36561320 (PubMed )
Supplement: Table2.xlsx › EGFR

Comparison of Resistance Spectra after First and Second Line Osimertinib Treatment Detected by Liquid Biopsy.

Jóri B et al.

Cancers, 2021

34201252 (PubMed )
Supplement: cancers-13-02861-s001.zip › cancers-1214406-supplementary.pdf

Plasma EGFR mutation abundance affects clinical response to first-line EGFR-TKIs in patients with advanced non-small cell lung cancer.

Wang X et al.

Annals of Translational Medicine, 2021

33987333 (PubMed )
Supplement: atm-09-08-635-supplementary.pdf

EGFR Exon 18 Mutations in Advanced Non-Small Cell Lung Cancer: A Real-World Study on Diverse Treatment Patterns and Clinical Outcomes.

Xu H et al.

Frontiers in Oncology, 2021

Spectrum of driver mutations and clinical impact of circulating tumor DNA analysis in non-small cell lung cancer: Analysis of over 8000 cases.

Mack PC et al.

Cancer, 2020

Target-based genomic profiling of ctDNA from Chinese non-small cell lung cancer patients: a result of real-world data.

Chen H et al.

Journal of Cancer Research and Clinical Oncology, 2020

EGFR-mutated lung adenocarcinomas from patients who progressed on EGFR-inhibitors show high engraftment rates in xenograft models.

Martins-Filho SN et al.

Lung Cancer (amsterdam, Netherlands), 2020

Clinical Utility of Targeted Sequencing in Lung Cancer: Experience From an Autonomous Swedish Health Care Center.

Isaksson S et al.

Jto Clinical and Research Reports, 2020

Concurrent RB1 and TP53 Alterations Define a Subset of EGFR-Mutant Lung Cancers at risk for Histologic Transformation and Inferior Clinical Outcomes.

Offin M et al.

Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer, 2019

Clinical and Molecular Characteristics of Thalamic Gliomas: Retrospective Report of 26 Cases.

Liu Y et al.

World Neurosurgery, 2019

Tag-based next generation sequencing: a feasible and reliable assay for EGFR T790M mutation detection in circulating tumor DNA of non small cell lung cancer patients.

Dono M et al.

Molecular Medicine (cambridge, Mass.), 2019

Oncogenic driver mutations in Swiss never smoker patients with lung adenocarcinoma and correlation with clinicopathologic characteristics and outcome.

Grosse C et al.

Plos One, 2019

PD-L1 mRNA expression in EGFR-mutant lung adenocarcinoma.

Isobe K et al.

Oncology Reports, 2018

Concomitant driver mutations in advanced EGFR-mutated non-small-cell lung cancer and their impact on erlotinib treatment.

Jakobsen JN et al.

Oncotarget, 2018

Clinical characteristics of non-small cell lung cancer harboring mutations in exon 20 of EGFR or HER2.

Takeda M et al.

Oncotarget, 2018

Comprehensive genomic profiling of lung cancer using a validated panel to explore therapeutic targets in East Asian patients.

Liu L et al.

Cancer Science, 2017

Mutations of the Epidermal Growth Factor Receptor Gene in Triple-Negative Breast Cancer.

Kim A et al.

Journal of Breast Cancer, 2017

Prevalence of EGFR and ALK Mutations in Lung Adenocarcinomas in the Levant Area - a Prospective Analysis

Tfayli A et al.

Asian Pacific Journal of Cancer Prevention : Apjcp, 2017

Case report: Durable response to afatinib in a patient with lung cancer harboring two uncommon mutations of EGFR and a KRAS mutation.

Tanizaki J et al.

Lung Cancer (amsterdam, Netherlands), 2016

Intertumor heterogeneity of non-small-cell lung carcinomas revealed by multiplexed mutation profiling and integrative genomics.

Tan DS et al.

International Journal of Cancer, 2014

24482041 (PubMed )
Supplement: supplement_1.docx

Novel p53 codon 240 Ser > Thr coding region mutation in the patients of oral squamous cell carcinoma (OSCC).

Saleem S et al.

Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine, 2014

In situ mutation detection and visualization of intratumor heterogeneity for cancer research and diagnostics.

Grundberg I et al.

Oncotarget, 2013

24280411 (PubMed )
Supplement: oncotarget-04-2407-s001.docx

The impact of EGFR mutation status on outcomes in patients with resected stage I non-small cell lung cancers.

Izar B et al.

The Annals of Thoracic Surgery, 2013

Implementing multiplexed genotyping of non-small-cell lung cancers into routine clinical practice.

Sequist LV et al.

Annals of Oncology : Official Journal of the European Society for Medical Oncology, 2011

Prognostic implication of EGFR, KRAS, and TP53 gene mutations in a large cohort of Japanese patients with surgically treated lung adenocarcinoma.

Kosaka T et al.

Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer, 2009

Epidemiology of doublet/multiplet mutations in lung cancers: evidence that a subset arises by chronocoordinate events.

Chen Z et al.

Plos One, 2008

19005564 (PubMed )
Supplement: pone.0003714.s003.xls › Table_S-1

Clinical and biological features associated with epidermal growth factor receptor gene mutations in lung cancers.

Shigematsu H et al.

Journal of the National Cancer Institute, 2005

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