Varaico: Literature-Extracted Genetic Variants

Gene:KRAS
Variant:p.Q99L
Back to variants list

KRAS

NM_004985.5:p.Q99L

Associated Papers

Genomic landscape of clinically acquired resistance alterations in patients treated with KRASG12C inhibitors.

Riedl JM et al.

Annals of Oncology : Official Journal of the European Society for Medical Oncology, 2025

Comprehensive structure-function analysis reveals gain- and loss-of-function mechanisms impacting oncogenic KRAS activity.

Kwon JJ et al.

Biorxiv : the Preprint Server for Biology, 2024

39484452 (PubMed )
Supplement: media-2.zip › Extended_Data_Tables › Extended_Data_Table_3.xlsx › KRAS_G12D_LOF_DMS_Screens

Site-specific mutagenesis screening in KRASG12D mutant library to uncover resistance mechanisms to KRASG12D inhibitors.

Choi J et al.

Cancer Letters, 2024

Oncogenic alterations in advanced NSCLC: a molecular super-highway.

Friedlaender A et al.

Biomarker Research, 2024

Abnormalities in the KRAS Gene and Treatment Options for NSCLC Patients with the G12C Mutation in This Gene-A Literature Review and Single-Center Experience.

Rekowska AK et al.

Biomedicines, 2024

Assessment of KRASG12C inhibitors for colorectal cancer.

Piazza GA et al.

Frontiers in Oncology, 2024

Single-Agent Divarasib (GDC-6036) in Solid Tumors with a KRAS G12C Mutation.

Sacher A et al.

The New England Journal of Medicine, 2023

Targeting KRASp.G12C Mutation in Advanced Non-Small Cell Lung Cancer: a New Era Has Begun.

Bungaro M et al.

Current Treatment Options in Oncology, 2022

Molecular Biology and Therapeutic Perspectives for K-Ras Mutant Non-Small Cell Lung Cancers.

Cekani E et al.

Cancers, 2022

Direct Targeting KRAS Mutation in Non-Small Cell Lung Cancer: Focus on Resistance.

Reita D et al.

Cancers, 2022

Understanding the influence of AMG 510 on the structure of KRASG12C empowered by molecular dynamics simulation.

Li Y et al.

Computational and Structural Biotechnology Journal, 2022

35284050 (PubMed )
Supplement: mmc1.docx

Mixed lineage kinase 3 gene mutations in mismatch repair deficient gastrointestinal tumours.

Velho S et al.

Human Molecular Genetics, 2010

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."