Varaico: Literature-Extracted Genetic Variants

Gene:EGFR
Variant:p.I789M
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EGFR

NM_005228.5:p.I789M

Associated Papers

EGFR mutations in sinonasal squamous neoplasms: Novel hotspot for exon 20 insertions.

Srivastava K et al.

Virchows Archiv : an International Journal of Pathology, 2025

ERBB family fusions are recurrent and actionable oncogenic targets across cancer types.

Schubert L et al.

Frontiers in Oncology, 2023

37168365 (PubMed )
Supplement: Table_4.xlsx › EGFR_mutations

Spectrum of EGFR aberrations and potential clinical implications: insights from integrative pan-cancer analysis.

Liu H et al.

Cancer Communications (london, England), 2020

32067422 (PubMed )
Supplement: CAC2-40-43-s001.xlsx › Table_S1

Genomic Profiling of Driver Gene Mutations in Chinese Patients With Non-Small Cell Lung Cancer.

Meng H et al.

Frontiers in Genetics, 2019

Integrative omics analyses broaden treatment targets in human cancer.

Sengupta S et al.

Genome Medicine, 2018

30053901 (PubMed )
Supplement: 13073_2018_564_MOESM2_ESM.xlsx › 13

Protein-structure-guided discovery of functional mutations across 19 cancer types.

Niu B et al.

Nature Genetics, 2016

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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."