Varaico: Literature-Extracted Genetic Variants

Gene:NTRK3
Variant:p.G623R
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NTRK3

NM_001012338.3:p.G623R

Associated Papers

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

Improving Global Access to Genomic Profiling in Rare Pediatric Cancers.

Farouk Sait S et al.

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

A comprehensive database for identifying and interpreting ctDNA driver genes and variants in cancer.

Wang Y et al.

Scientific Data, 2025

40670358 (PubMed )
Supplement: 41597_2025_5550_MOESM1_ESM.xls › Table_S5

Mechanisms of resistance to RET-directed therapies.

Clifton-Bligh RJ

Endocrine-related Cancer, 2025

Advances in predicting breast cancer driver mutations: Tools for precision oncology (Review).

Hao W et al.

International Journal of Molecular Medicine, 2025

RNA hybrid-capture next-generation sequencing has high sensitivity in identifying known and less characterized oncogenic and likely oncogenic NTRK fusions in a real-world standard-of-care setting.

Wallen ZD et al.

Frontiers in Genetics, 2025

40385986 (PubMed )
Supplement: Supplementaryfile1.xlsx › Supplementary_Table_3

A Novel Oncogenic and Drug-Sensitive KIF5B-NTRK1 Fusion in Lung Adenocarcinoma.

Li H et al.

Current Oncology (toronto, Ont.), 2024

ERK signaling promotes resistance to TRK kinase inhibition in NTRK fusion-driven glioma mouse models.

Schmid S et al.

Cell Reports, 2024

BPI-28592 as a novel second generation inhibitor for NTRK fusion tumors.

Sheng J et al.

Npj Precision Oncology, 2024

Zurletrectinib is a next-generation TRK inhibitor with strong intracranial activity against NTRK fusion-positive tumours with on-target resistance to first-generation agents.

Roa P et al.

British Journal of Cancer, 2024

Liquid Biopsy Profiling with Multiple Tests in Patients with Metastatic Breast Cancer.

Higa N et al.

Journal of Molecular Pathology, 2024

41614092 (PubMed )
Supplement: NIHMS2059476-supplement-Supplementary_Material.pdf

Clinical utility of plasma cell-free DNA in pancreatic neuroendocrine neoplasms.

Cowzer D et al.

Endocrine-related Cancer, 2024

Adaptive Darwinian off-target resistance mechanisms to selective RET inhibition in RET driven cancer.

Subbiah V et al.

Npj Precision Oncology, 2024

Oncogenic alterations in advanced NSCLC: a molecular super-highway.

Friedlaender A et al.

Biomarker Research, 2024

Critical domains for NACC2-NTRK2 fusion protein activation.

Yang W et al.

Plos One, 2024

China special issue on gastrointestinal tumors-NTRK fusion in a large real-world population and clinical utility of circulating tumor DNA genotyping to guide TRK inhibitor treatment.

Qi C et al.

International Journal of Cancer, 2023

HPV-positive clinically advanced squamous cell carcinoma of the urinary bladder (aBSCC): A comprehensive genomic profiling (CGP) study.

Ghelani GH et al.

Urologic Oncology, 2023

Prevalence and clinico-genomic characteristics of patients with TRK fusion cancer in China.

Xu Y et al.

Npj Precision Oncology, 2023

Actionability classification of variants of unknown significance correlates with functional effect.

Johnson A et al.

Npj Precision Oncology, 2023

37454202 (PubMed )
Supplement: 41698_2023_420_MOESM2_ESM.pdf

Development of a Cell Line Containing the Chimeric ETV6-NTRK3 Gene. The Search for Mutations of the Tyrosine Kinase Chimeric Domain That Cause Resistance to Larotrectinib.

Boyarskikh UA et al.

Bulletin of Experimental Biology and Medicine, 2023

Progressive metastatic infantile fibrosarcoma with multiple acquired mutations.

Furtado LV et al.

Cold Spring Harbor Molecular Case Studies, 2023

Kinase inhibitors in thyroid cancers.

Sukrithan V et al.

Endocrine Oncology (bristol, England), 2023

Targeting Gatekeeper Mutations for Kinase Drug Discovery.

Zhou Y et al.

Journal of Medicinal Chemistry, 2022

Kinase Fusion-Related Thyroid Carcinomas: Towards Predictive Models for Advanced Actionable Diagnostics.

Chu YH et al.

Endocrine Pathology, 2022

JND4135, a New Type II TRK Inhibitor, Overcomes TRK xDFG and Other Mutation Resistance In Vitro and In Vivo.

Wang J et al.

Molecules (basel, Switzerland), 2022

Exploring the kinase-inhibitor fragment interaction space facilitates the discovery of kinase inhibitor overcoming resistance by mutations.

Wang ZZ et al.

Briefings in Bioinformatics, 2022

Conformational adjustment overcomes multiple drug-resistance mutants of tropomyosin receptor kinase.

Mei LC et al.

European Journal of Medicinal Chemistry, 2022

Discovery of the First Highly Selective and Broadly Effective Macrocycle-Based Type II TRK Inhibitors that Overcome Clinically Acquired Resistance.

Wang Z et al.

Journal of Medicinal Chemistry, 2022

Somatic Genomic Testing in Patients With Metastatic or Advanced Cancer: ASCO Provisional Clinical Opinion.

Chakravarty D et al.

Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology, 2022

Tumor genomic profiling and personalized tracking of circulating tumor DNA in Vietnamese colorectal cancer patients.

Nguyen HT et al.

Frontiers in Oncology, 2022

36578946 (PubMed )
Supplement: DataSheet_1.pdf

DeteX: A highly accurate software for detecting SNV and InDel in single and paired NGS data in cancer research.

Cui Y et al.

Frontiers in Genetics, 2022

36685970 (PubMed )
Supplement: Table5.xlsx › Sheet1

Case report: Acquired neurotrophic tyrosine receptor kinase inhibitor resistance in a patient with pancreatic neuroendocrine carcinoma receiving entrectinib.

Wu WC et al.

Frontiers in Oncology, 2022

Molecular Characteristics of Repotrectinib That Enable Potent Inhibition of TRK Fusion Proteins and Resistant Mutations.

Murray BW et al.

Molecular Cancer Therapeutics, 2021

Discovery of Next-Generation Tropomyosin Receptor Kinase Inhibitors for Combating Multiple Resistance Associated with Protein Mutation.

Zhuo LS et al.

Journal of Medicinal Chemistry, 2021

Mechanisms of targeted therapy resistance in a pediatric glioma driven by ETV6-NTRK3 fusion.

Keddy C et al.

Cold Spring Harbor Molecular Case Studies, 2021

Targeting the NTRK Fusion Gene in Pancreatic Acinar Cell Carcinoma: A Case Report and Review of the Literature.

Gupta M et al.

Journal of the National Comprehensive Cancer Network : Jnccn, 2021

Resistance to Avapritinib in PDGFRA-Driven GIST Is Caused by Secondary Mutations in the PDGFRA Kinase Domain.

Grunewald S et al.

Cancer Discovery, 2021

TRK xDFG Mutations Trigger a Sensitivity Switch from Type I to II Kinase Inhibitors.

Cocco E et al.

Cancer Discovery, 2021

Targeted Therapy of Papillary Thyroid Cancer: A Comprehensive Genomic Analysis.

Hescheler DA et al.

Frontiers in Endocrinology, 2021

34630336 (PubMed )
Supplement: Table_1.xlsx › Tab2

NTRK kinase domain mutations in cancer variably impact sensitivity to type I and type II inhibitors.

Somwar R et al.

Communications Biology, 2020

[Chinese Expert Consensus on Next Generation Sequencing Diagnosis 
for Non-small Cell Lung Cancer (2020 Edition)].

Unknown Author

Zhongguo Fei Ai Za Zhi = Chinese Journal of Lung Cancer, 2020

Genomic Alteration in Metastatic Breast Cancer and Its Treatment.

Li A et al.

American Society of Clinical Oncology Educational Book. American Society of Clinical Oncology. Annual Meeting, 2020

Roles of TrkC Signaling in the Regulation of Tumorigenicity and Metastasis of Cancer.

Jin W

Cancers, 2020

Targeting non-small cell lung cancer: driver mutation beyond epidermal growth factor mutation and anaplastic lymphoma kinase fusion.

Chu QS

Therapeutic Advances in Medical Oncology, 2020

RET kinase alterations in targeted cancer therapy.

Liu X et al.

Cancer Drug Resistance (alhambra, Calif.), 2020

Structural basis of resistance of mutant RET protein-tyrosine kinase to its inhibitors nintedanib and vandetanib.

Terzyan SS et al.

The Journal of Biological Chemistry, 2019

Larotrectinib for paediatric solid tumours harbouring NTRK gene fusions: phase 1 results from a multicentre, open-label, phase 1/2 study.

Laetsch TW et al.

The Lancet. Oncology, 2018

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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."