Varaico: Literature-Extracted Genetic Variants

Gene:FLT3
Variant:p.R437Splc
Back to variants list

FLT3

NM_004119.3:p.R437Splc

Associated Papers

Mutational profiling using liquid biopsy to guide targeted therapy in patients with metastatic cancer.

Mazouji O et al.

Scientific Reports, 2025

40169620 (PubMed )
Supplement: 41598_2025_88094_MOESM1_ESM.xlsx › Feuil1

The Fusion Genes and Their Relation with Genetic Variants in Egyptian AML Patients.

Abo Elwafa RAH et al.

Asian Pacific Journal of Cancer Prevention : Apjcp, 2025

Next-generation sequencing as a valuable tool for mutational spectrum in advanced-stage NSCLC patients.

Iurca I et al.

Medicine and Pharmacy Reports, 2024

The carcinogenic capacity of arsenic in normal epithelial breast cells and double-positive breast cancer cells.

Zimta AA et al.

Medicine and Pharmacy Reports, 2024

Exonic splicing code and coordination of divalent metals in proteins.

Bakhtiar D et al.

Nucleic Acids Research, 2024

38055834 (PubMed )
Supplement: gkad1161_supplemental_files.zip › Supplementary_information-FORMATTED-revised.pdf

Cerebellar liponeurocytoma: clinical, histopathological and molecular features of a series of three cases, including one recurrent tumor.

Broggi G et al.

Neuropathology : Official Journal of the Japanese Society of Neuropathology, 2022

Single-Nucleotide Variations, Insertions/Deletions and Copy Number Variations in Myelodysplastic Syndrome during Disease Progression Revealed by a Single-Cell DNA Sequencing Platform.

Lee P et al.

International Journal of Molecular Sciences, 2022

35563039 (PubMed )
Supplement: ijms-23-04647-s001.zip › Supplemental_file_S2.xlsx › Supp_Table_S2

Next-Generation Sequencing in Lung Cancer Patients: A Comparative Approach in NSCLC and SCLC Mutational Landscapes.

Pop-Bica C et al.

Journal of Personalized Medicine, 2022

35330454 (PubMed )
Supplement: jpm-12-00453-s001.zip › jpm-1596007-supplementary.xlsx › Blood

The Molecular Subtype of Adult Acute Lymphoblastic Leukemia Samples Determines the Engraftment Site and Proliferation Kinetics in Patient-Derived Xenograft Models.

Richter A et al.

Cells, 2022

Pancreatic Cancer-Related Mutational Burden Is Not Increased in a Patient Cohort With Clinically Severe Chronic Pancreatitis.

Cowan RW et al.

Clinical and Translational Gastroenterology, 2021

34797250 (PubMed )
Supplement: ct9-12-e00431-s005.xlsx › SDC5

Detection of activating mutations in liquid biopsy of Egyptian breast cancer patients using targeted next-generation sequencing: a pilot study.

Kassem N et al.

Journal of the Egyptian National Cancer Institute, 2021

Microsecond-timescale MD simulation of EGFR minor mutation predicts the structural flexibility of EGFR kinase core that reflects EGFR inhibitor sensitivity.

Yoshizawa T et al.

Npj Precision Oncology, 2021

33863983 (PubMed )
Supplement: 41698_2021_170_MOESM4_ESM.xlsx › Pre_Post_Afatinibshared_variant

Higher Mutation Burden in High Proliferation Compartments of Heterogeneous Melanoma Tumors.

Grzywa TM et al.

International Journal of Molecular Sciences, 2021

Adamantinomatous Craniopharyngioma in an Adult: A Case Report with NGS Analysis.

Jastania RA et al.

International Medical Case Reports Journal, 2020

Cutaneous metastasis as a primary presentation of a pulmonary enteric adenocarcinoma.

Todisco A et al.

The International Journal of Biological Markers, 2019

Identification of a novel somatic mutation of POU6F2 by whole-genome sequencing in prolactinoma.

Miao Y et al.

Molecular Genetics & Genomic Medicine, 2019

Development and validation of a targeted gene sequencing panel for application to disparate cancers.

McCabe MJ et al.

Scientific Reports, 2019

31745186 (PubMed )
Supplement: 41598_2019_52000_MOESM2_ESM.xlsx › Sheet1

Connecting the dots between different networks: miRNAs associated with bladder cancer risk and progression.

Braicu C et al.

Journal of Experimental & Clinical Cancer Research : Cr, 2019

31665050 (PubMed )
Supplement: 13046_2019_1406_MOESM9_ESM.xlsx › NGS_all_data

Clinical Validation of Discordant Trunk Driver Mutations in Paired Primary and Metastatic Lung Cancer Specimens.

Tseng LH et al.

American Journal of Clinical Pathology, 2019

Differences in Mutational Profile between Follicular Thyroid Carcinoma and Follicular Thyroid Adenoma Identified Using Next Generation Sequencing.

Borowczyk M et al.

International Journal of Molecular Sciences, 2019

31248021 (PubMed )
Supplement: ijms-20-03126-s001.pdf

Mutation profiling of anaplastic ependymoma grade III by Ion Proton next generation DNA sequencing.

Butt E et al.

F1000research, 2019

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

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."