Varaico: Literature-Extracted Genetic Variants

Gene:EGFR
Variant:p.C240S
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EGFR

NM_005228.5:p.C240S

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

Spatial multi-omics unveils the monoclonal origin, neuroendocrine plasticity, and microenvironment niches in combined small cell lung cancer.

Wang Z et al.

Biorxiv : the Preprint Server for Biology, 2026

Integrating evidence from protein domains to identify cancer driver mutations.

Ostroverkhova D et al.

Protein Science : a Publication of the Protein Society, 2026

41556616 (PubMed )
Supplement: PRO-35-e70422-s002.xlsx › Table_S1

EGFR mutation spectrum and clinical correlations in Tunisian Non-Small cell lung cancer patients.

Abdelmaksoud-Dammak R et al.

Molecular Biology Reports, 2026

Optimizing communication for ultrafast lung cancer biomarker testing: the UTOPIA pilot study.

Hernandez S et al.

Lung Cancer (amsterdam, Netherlands), 2026

Efficacy of TKIs in non-small cell lung cancer with atypical EGFR p.L747P and p.L747S mutations.

Hu Q et al.

Frontiers in Oncology, 2026

Refining treatment strategies for non-small cell lung cancer lacking actionable mutations: insights from multi-omics studies.

Rocca A et al.

British Journal of Cancer, 2025

Challenges associated with the treatment of E709K and L858R double mutation in lung adenocarcinoma: A case report and literature review.

Song J et al.

Oncology Letters, 2025

Single-cell RNA profiling reveals an immunosuppressive microenvironment in EGFR double-mutant non-small cell lung cancer.

Yang J et al.

Translational Lung Cancer Research, 2025

41234595 (PubMed )
Supplement: tlcr-14-10-4235-supplementary.pdf

Discriminating activating, deactivating and resistance variants in protein kinases.

Singh G et al.

Genome Medicine, 2025

41152984 (PubMed )
Supplement: 13073_2025_1564_MOESM2_ESM.xlsx › Table_S6

Genetic Alteration Profiling in North Macedonian Lung Cancer Patients.

Eftimov A et al.

Genes, 2025

Discovery of Novel RASGRF2 Fusions as a Therapeutic Target in Lung Adenocarcinoma of Never or Light Smokers.

Terashima Y et al.

Cancer Science, 2025

40734624 (PubMed )
Supplement: CAS-116-2868-s002.xlsx › Table_S3

Clinical Outcomes of Later-Generation EGFR-TKIs for Uncommon EGFR Mutations in NSCLC: A Multicenter Real-World Study.

Shigematsu L et al.

Thoracic Cancer, 2025

Oncogenic driver mutations underlie the spatial tumour immune landscape of non-small cell lung cancer.

Hartner S et al.

Nature Communications, 2025

40998804 (PubMed )
Supplement: 41467_2025_63465_MOESM2_ESM.xlsx › Sheet1

Current paradigm of EGFRins20 in non-small cell lung cancer: A long way forward.

Miyamura BV et al.

Med (new York, N.y.), 2025

Saturation profiling of drug-resistant genetic variants using prime editing.

Kim Y et al.

Nature Biotechnology, 2025

Lazertinib for Patients with NSCLC Harboring Uncommon EGFR Mutations: A Phase II Multicenter Trial.

Park S et al.

Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer, 2025

Phase II study of afatinib for advanced non-small cell lung cancer with uncommon epidermal growth factor receptor mutations, including compound mutations detected by next-generation sequencing.

Mamesaya N et al.

International Journal of Clinical Oncology, 2025

Rare mutations at EGFR L747 position: molecular characteristics and superior response to afatinib in NSCLC patients.

Huang Y et al.

Esmo Open, 2025

40834500 (PubMed )
Supplement: mmc7.docx

A universal approach for mutation identification with a DNA probe-enzyme combination platform.

Li B et al.

Analytical Methods : Advancing Methods and Applications, 2025

On-target toxicity limits the efficacy of CDK11 inhibition against cancers with 1p36 deletions.

Julian L et al.

Biorxiv : the Preprint Server for Biology, 2025

40766692 (PubMed )
Supplement: media-14.xlsx › Table_S14_-_KINOMEscan_data

Rare sequential EGFR and ALK mutations in non-small cell lung cancer: A case report and literature review.

Nguyen HV et al.

Oncology Letters, 2025

Case Report: A Bilateral Synchronous Primary Non-Small Cell Lung Cancer Patient With Two Different EGFR Mutations.

Quach TD et al.

Cancer Reports (hoboken, N.j.), 2025

Exceptional Response to Immunotherapy-based Treatment in Compound EGFR-Mutated Oligometastatic Pulmonary Sarcomatoid Carcinoma: A Case Report.

Gianchandani A et al.

Journal of Immunotherapy and Precision Oncology, 2025

Spectrum of rare EGFR mutations in Indonesian lung adenocarcinoma: Findings from an 8-year analysis of 4,778 cases highlighting the need for advanced targeted therapies.

Heriyanto DS et al.

Narra J, 2025

STX-721, a Covalent EGFR/HER2 Exon 20 Inhibitor, Utilizes Exon 20-Mutant Dynamic Protein States and Achieves Unique Mutant Selectivity Across Human Cancer Models.

Pagliarini RA et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2025

40465424 (PubMed )
Supplement: ccr-24-3833_supplementary_tables1_suppts1.xlsx › Table_2_-_kinomescan

An in-depth exploration of four heterogeneity structure-based EGFR mutation subgroups in Chinese non-small cell lung cancer.

Yu Y et al.

Bmc Pulmonary Medicine, 2025

40611150 (PubMed )
Supplement: 12890_2025_3774_MOESM1_ESM.xlsx › Sheet1

Brief Report: The Genomic Landscape of Small Cell Lung Cancer in Never-Smoking Patients.

Oh MS et al.

Clinical Lung Cancer, 2025

Assessing mutation-clinical correlations and treatment outcomes in Vietnamese non-small cell lung cancer patients.

Nguyen HB et al.

Practical Laboratory Medicine, 2025

Tissue-based genomic profiling of 300,000 tumors highlights the detection of variants with low allele fraction.

Sisoudiya SD et al.

Npj Precision Oncology, 2025

Reannotation of cancer mutations based on expressed RNA transcripts reveals functional non-coding mutations in melanoma.

Pepe D et al.

American Journal of Human Genetics, 2025

40359938 (PubMed )
Supplement: mmc6.xlsx › Sheet_1

Absence of KRAS Mutation as an Indicator of Pancreatic Metastasis Originating From Lung Cancer: A Case Report.

Suzuki S et al.

Cureus, 2025

Detection of actionable mutations in circulating tumor DNA for non-small cell lung cancer patients.

van der Leest P et al.

Communications Medicine, 2025

40437208 (PubMed )
Supplement: 43856_2025_921_MOESM4_ESM.xlsx › Blad1

Complementary modes of resistance to EGFR TKI in lung adenocarcinoma through MAPK activation and cellular plasticity.

Zatzman M et al.

Biorxiv : the Preprint Server for Biology, 2025

40654861 (PubMed )
Supplement: media-1.xlsx › Table_S1_-_Cohort_Metadata

Dual Disruption of DNA Repair by a Novel CHK2 Inhibitor, ART-446, and Olaparib is a Promising Strategy for Triple-Negative Breast Cancer Therapy.

Kang HJ et al.

Biomolecules & Therapeutics, 2025

40195731 (PubMed )
Supplement: bt-33-3-458-supple.pdf

Molecular Testing for EGFR Mutation in Moroccan NSCLC Patients: CHU Hassan II-Fez Experience.

Boukansa S et al.

International Journal of Surgical Pathology, 2025

Development and validation of machine learning models based on molecular features for estimating the probability of multiple primary lung carcinoma versus intrapulmonary metastasis in patients presenting multiple non-small cell lung cancers.

Liu N et al.

Translational Lung Cancer Research, 2025

40386724 (PubMed )
Supplement: tlcr-14-04-1118-supplementary.pdf

Prevalence of EGFR gene mutations in patients with early-stage resectable non-small cell lung cancer in Spain: the ORIGEN study.

Varela M et al.

Translational Lung Cancer Research, 2025

40386732 (PubMed )
Supplement: tlcr-14-04-1254-supplementary.pdf

Prevalence and breakdown of KRAS driver mutations in a large UK non-small cell lung cancer cohort.

Niesner ICC et al.

Journal of Clinical Pathology, 2025

Investigating the frequencies of EGFR mutations and EGFR single nucleotide polymorphisms genotypes and their predictive role in NSCLC patients in Republic of Serbia.

Obradović J et al.

Molecular Biology Reports, 2025

Decoding the Clinical and Molecular Signatures of EGFR Common, Compound, and Uncommon Mutations in NSCLC: A Brief Report.

Tavernari D et al.

Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer, 2025

Rare exon 18 G719A and exon 21 L833V compound EGFR mutations show favorable response to Third-Generation TKI Furmonertinib: A case report and literature review.

Yuejian et al.

Investigational New Drugs, 2025

Amivantamab as a salvage therapy post-EGFR-tyrosine kinase inhibitor failure in patients with mutated EGFR non-small cell lung cancer.

Krayim B et al.

Translational Lung Cancer Research, 2025

Real-World Performance of the EasyPGX® Ready Epidermal Growth Factor Receptor Assay for Genomic Testing of Non-Small Cell Lung Cancer Samples.

Schmid MB et al.

Biomedicines, 2025

40299437 (PubMed )
Supplement: biomedicines-13-00814-s001.zip › biomedicines-3506106-supplementary.pdf

Comparative analysis of RNA expression in a single institution cohort of pediatric cancer patients.

Vasquez YA et al.

Npj Precision Oncology, 2025

40119139 (PubMed )
Supplement: 41698_2025_852_MOESM11_ESM.xlsx › Supplementary_Data_9

A Cross-Sectional Study of Variant Interpretation and Reporting of NGS Data Using Tertiary Analysis Software: Navify® Mutation Profiler.

Pepe F et al.

Oncology and Therapy, 2025

Multicenter In-House Evaluation of an Amplicon-Based Next-Generation Sequencing Panel for Comprehensive Molecular Profiling.

Jantus-Lewintre E et al.

Molecular Diagnosis & Therapy, 2025

39798063 (PubMed )
Supplement: 40291_2024_766_MOESM2_ESM.xlsx › S1c-Control_D_2_HD827
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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."