Varaico: Literature-Extracted Genetic Variants

Gene:FGFR4
Variant:p.V550M
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FGFR4

NM_213647.3:p.V550M

Associated Papers

FGFR Testing in Metastatic Urothelial Carcinoma-Who, When, and How to Test.

Mansinho A et al.

Cancers, 2026

Saturation mutagenesis identifies activating and resistance-inducing FGFR kinase domain mutations.

Tangermann C et al.

Nature Genetics, 2026

41361008 (PubMed )
Supplement: 41588_2025_2431_MOESM3_ESM.xlsx › S7_Reported_resistance

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_S5

Association of phosphorylation status of ERK and genetic MAPK alterations in pediatric tumors.

Selt F et al.

Scientific Reports, 2025

Non-small cell lung carcinoma with clear cell features: a clinicopathologic, immunohistochemical, and molecular study of 31 cases.

Suster DI et al.

Virchows Archiv : an International Journal of Pathology, 2024

Standing in the canine precision medicine knowledge gap: Improving annotation of canine cancer genomic biomarkers through systematic comparative analysis of human cancer mutations in COSMIC.

Sakthikumar S et al.

Veterinary and Comparative Oncology, 2023

37248814 (PubMed )
Supplement: supplement_1.xlsx › Supp._Table_5

Validation and Clinical Application of ONCOaccuPanel for Targeted Next-Generation Sequencing of Solid Tumors.

Kim M et al.

Cancer Research and Treatment, 2023

36470260 (PubMed )
Supplement: crt-2022-891-Supplementary-Table-2.pdf

The landscape of actionable genomic alterations in lung adenocarcinomas in India.

Sharma R et al.

Frontiers in Genetics, 2023

Discovery of 2-Amino-7-sulfonyl-7H-pyrrolo[2,3-d]pyrimidine Derivatives as Potent Reversible FGFR Inhibitors with Gatekeeper Mutation Tolerance: Design, Synthesis, and Biological Evaluation.

Xie W et al.

Journal of Medicinal Chemistry, 2022

Targeting Gatekeeper Mutations for Kinase Drug Discovery.

Zhou Y et al.

Journal of Medicinal Chemistry, 2022

Multiparametric and accurate functional analysis of genetic sequence variants using CRISPR-Select.

Niu Y et al.

Nature Genetics, 2022

Design, Synthesis, and Biological Evaluation of 5-Formyl-pyrrolo[3,2-b]pyridine-3-carboxamides as New Selective, Potent, and Reversible-Covalent FGFR4 Inhibitors.

Yang F et al.

Journal of Medicinal Chemistry, 2022

Identification of novel prognostic and predictive biomarkers in salivary duct carcinoma via comprehensive molecular profiling.

Kohsaka S et al.

Npj Precision Oncology, 2022

36333410 (PubMed )
Supplement: 41698_2022_324_MOESM3_ESM.xlsx › Mutations

Characterization of the cholangiocarcinoma drug pemigatinib against FGFR gatekeeper mutants.

Lin Q et al.

Communications Chemistry, 2022

Fibroblast Growth Factor Receptor 1-4 Genetic Aberrations as Clinically Relevant Biomarkers in Squamous Cell Lung Cancer.

Moes-Sosnowska J et al.

Frontiers in Oncology, 2022

Intrinsic relative preference profile of pan-kinase inhibitor drug staurosporine towards the clinically occurring gatekeeper mutations in Protein Tyrosine Kinases.

Ren Z et al.

Computational Biology and Chemistry, 2021

Selective FGFR/FGF pathway inhibitors: inhibition strategies, clinical activities, resistance mutations, and future directions.

Repetto M et al.

Expert Review of Clinical Pharmacology, 2021

Comprehensive characterization of distinct genetic alterations in metastatic breast cancer across various metastatic sites.

Cha S et al.

Npj Breast Cancer, 2021

34272397 (PubMed )
Supplement: 41523_2021_303_MOESM2_ESM.pdf

Validation of a liquid biopsy assay with molecular and clinical profiling of circulating tumor DNA.

Finkle JD et al.

Npj Precision Oncology, 2021

34215841 (PubMed )
Supplement: 41698_2021_202_MOESM1_ESM.pdf

Next-Generation Sequencing Identifies Potential Actionable Targets in Paediatric Sarcomas.

Juan Ribelles A et al.

Journal of Personalized Medicine, 2021

Fibroblast growth factor receptors in cancer: genetic alterations, diagnostics, therapeutic targets and mechanisms of resistance.

Krook MA et al.

British Journal of Cancer, 2021

FGFR4: A promising therapeutic target for breast cancer and other solid tumors.

Levine KM et al.

Pharmacology & Therapeutics, 2020

Characterization of FGF401 as a reversible covalent inhibitor of fibroblast growth factor receptor 4.

Zhou Z et al.

Chemical Communications (cambridge, England), 2019

LY2874455 potently inhibits FGFR gatekeeper mutants and overcomes mutation-based resistance.

Wu D et al.

Chemical Communications (cambridge, England), 2018

Nonamplification ERBB2 genomic alterations in 5605 cases of recurrent and metastatic breast cancer: An emerging opportunity for anti-HER2 targeted therapies.

Ross JS et al.

Cancer, 2016

FGFR inhibitors: Effects on cancer cells, tumor microenvironment and whole-body homeostasis (Review).

Katoh M

International Journal of Molecular Medicine, 2016

Landscape of activating cancer mutations in FGFR kinases and their differential responses to inhibitors in clinical use.

Patani H et al.

Oncotarget, 2016

Functions of Fibroblast Growth Factor Receptors in cancer defined by novel translocations and mutations.

Gallo LH et al.

Cytokine & Growth Factor Reviews, 2015

Novel mutations in neuroendocrine carcinoma of the breast: possible therapeutic targets.

Ang D et al.

Applied Immunohistochemistry & Molecular Morphology : Aimm, 2015

Structural insights into FGFR kinase isoform selectivity: diverse binding modes of AZD4547 and ponatinib in complex with FGFR1 and FGFR4.

Tucker JA et al.

Structure (london, England : 1993), 2014

Structure-functional prediction and analysis of cancer mutation effects in protein kinases.

Dixit A et al.

Computational and Mathematical Methods in Medicine, 2014

High-resolution array CGH identifies common mechanisms that drive embryonal rhabdomyosarcoma pathogenesis.

Paulson V et al.

Genes, Chromosomes & Cancer, 2011

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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."