Varaico: Literature-Extracted Genetic Variants

Gene:BRAF
Variant:p.G469*
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BRAF

NM_004333.6:p.G469*

Associated Papers

Diversity of BRAF mutations in non-small cell lung cancer and implications on treatment.

Lu K et al.

Npj Precision Oncology, 2025

Outcomes with frontline immune checkpoint inhibitors among individuals with BRAF-mutant non-small cell lung cancer.

Marin-Acevedo JA et al.

Frontiers in Oncology, 2025

Genomic profiles and their associations with microsatellite instability status, tumor mutational burden, and programmed death ligand 1 expression in Chinese patients with colorectal cancer.

Luo B et al.

Journal of Gastrointestinal Oncology, 2024

Comprehensive Genomic Analysis of Patients With Non-Small-Cell Lung Cancer Using Blood-Based Circulating Tumor DNA Assay: Findings From the BFAST Database of a Single Center in Taiwan.

Wang HY et al.

Jco Precision Oncology, 2024

Biomarker testing in lung cancer: from bench to bedside.

Batra U et al.

Oncology Reviews, 2024

Long term activity of vemurafenib in cancers with BRAF mutations: the ACSE basket study for advanced cancers other than BRAFV600-mutated melanoma.

Blay JY et al.

Esmo Open, 2023

37922690 (PubMed )
Supplement: mmc2.docx

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

Genomic and transcriptomic insights into the precision treatment of pulmonary enteric adenocarcinoma.

Liu Y et al.

Lung Cancer (amsterdam, Netherlands), 2023

Case report: targeted sequencing improves the diagnosis of multiple synchronous lung cancers.

Ba Y et al.

Translational Lung Cancer Research, 2023

The Genomics of Colorectal Cancer in Populations with African and European Ancestry.

Myer PA et al.

Cancer Discovery, 2022

Custom multi‑tumor next‑generation sequencing panel for routine molecular diagnosis of solid tumors: Validation and results from three‑year clinical use.

Chevrier S et al.

International Journal of Molecular Medicine, 2022

35244186 (PubMed )
Supplement: Supplementary_Data2.xlsx › Feuil1

Spectrum of BRAF Aberrations and Its Potential Clinical Implications: Insights From Integrative Pan-Cancer Analysis.

Yi Q et al.

Frontiers in Bioengineering and Biotechnology, 2022

35910024 (PubMed )
Supplement: Table2.XLSX › table

Genomic Landscape of RTK/RAS Pathway and Tumor Immune Infiltration as Prognostic Indicator of Lung Adenocarcinoma.

Yin XQ et al.

Frontiers in Oncology, 2022

35936718 (PubMed )
Supplement: Table_4.xlsx › MAF_infomation

Genomic profiles and their associations with TMB, PD-L1 expression, and immune cell infiltration landscapes in synchronous multiple primary lung cancers.

Hu C et al.

Journal for Immunotherapy of Cancer, 2021

Genomic profile of advanced breast cancer in circulating tumour DNA.

Kingston B et al.

Nature Communications, 2021

Identifying Actionable Variants Using Capture-Based Targeted Sequencing in 563 Patients With Non-Small Cell Lung Carcinoma.

Jiang H et al.

Frontiers in Oncology, 2021

35186718 (PubMed )
Supplement: Table_1.xlsx › Supplementary_Table_2

Positive Correlation Between Somatic Mutations in RAS Gene and Colorectal Cancer in Telangana Population: Hospital-Based Study in a Cosmopolitan City.

Goud KI et al.

Applied Biochemistry and Biotechnology, 2020

The association between BRAF mutation class and clinical features in BRAF-mutant Chinese non-small cell lung cancer patients.

Lin Q et al.

Journal of Translational Medicine, 2019

V600E BRAF versus Non-V600E BRAF Mutated Lung Adenocarcinomas: Cytomorphology, Histology, Coexistence of Other Driver Mutations and Patient Characteristics.

Salimian KJ et al.

Acta Cytologica, 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."