Varaico: Literature-Extracted Genetic Variants

Gene:FGFR3
Variant:p.M528I
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FGFR3

NM_000142.5:p.M528I

Associated Papers

Harnessing genomic profiling for improved urothelial cancer outcomes.

Yu EM et al.

Expert Review of Anticancer Therapy, 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_S6

Prevalence and biological impact of clinically relevant gene fusions in head and neck cancers.

Hoskins EL et al.

Npj Precision Oncology, 2025

40610725 (PubMed )
Supplement: 41698_2025_889_MOESM5_ESM.xlsx › Sheet1

Pemigatinib for metastatic or surgically unresectable urothelial carcinoma with FGF/FGFR genomic alterations: final results from FIGHT-201.

Necchi A et al.

Annals of Oncology : Official Journal of the European Society for Medical Oncology, 2024

Fibroblast growth factor receptor 3 mutation attenuates response to immune checkpoint blockade in metastatic urothelial carcinoma by driving immunosuppressive microenvironment.

Song Y et al.

Journal for Immunotherapy of Cancer, 2023

37777251 (PubMed )
Supplement: jitc-2022-006643supp001.pdf

Identification of copy number variation-driven molecular subtypes informative for prognosis and treatment in pancreatic adenocarcinoma of a Chinese cohort.

Zhan Q et al.

Ebiomedicine, 2021

34839264 (PubMed )
Supplement: mmc5.xlsx › Sheet1

Tumor fraction-guided cell-free DNA profiling in metastatic solid tumor patients.

Tsui DWY et al.

Genome Medicine, 2021

34059130 (PubMed )
Supplement: 13073_2021_898_MOESM3_ESM.xlsx › SuppTable1

Phase and context shape the function of composite oncogenic mutations.

Gorelick AN et al.

Nature, 2020

32461694 (PubMed )
Supplement: NIHMS1582596-supplement-1582596_Supp_Tab1-5.xlsx › Table_S2._Composite_mutations

A novel S269C mutation in fibroblast growth factor receptor 3 in a Japanese child with hypochondroplasia.

Takahashi I et al.

Human Genome Variation, 2018

Inhibitor repurposing reveals ALK, LTK, FGFR, RET and TRK kinases as the targets of AZD1480.

Gudernova I et al.

Oncotarget, 2017

29312610 (PubMed )
Supplement: oncotarget-08-109319-s003.docx

Achondroplasia: Development, pathogenesis, and therapy.

Ornitz DM et al.

Developmental Dynamics : an Official Publication of the American Association of Anatomists, 2017

Elucidation of a four-site allosteric network in fibroblast growth factor receptor tyrosine kinases.

Chen H et al.

Elife, 2017

Fibroblast growth factor signaling in skeletal development and disease.

Ornitz DM et al.

Genes & Development, 2015

A novel variant of FGFR3 causes proportionate short stature.

Kant SG et al.

European Journal of Endocrinology, 2015

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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."