Varaico: Literature-Extracted Genetic Variants

Gene:STK11
Variant:p.G163R
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STK11

NM_000455.5:p.G163R

Associated Papers

Comprehensive genomic and transcriptomic analysis enables molecularly guided therapy options in peritoneal and pleural mesothelioma.

Möhrmann L et al.

Esmo Open, 2025

40174508 (PubMed )
Supplement: mmc2.xlsx › Suppl._Data_7

Evaluating predictors of kinase activity of STK11 variants identified in primary human non-small cell lung cancers.

Chen Y et al.

Human Genetics, 2025

Exploring the histogenesis of STK11 adnexal tumour using electron microscopy.

Mascaro N et al.

Virchows Archiv : an International Journal of Pathology, 2024

Evaluating predictors of kinase activity of STK11 variants identified in primary human non-small cell lung cancers.

Chen Y et al.

Research Square, 2024

Clinical perspectives on the value of testing for STK11 and KEAP1 mutations in advanced NSCLC.

Shiller M et al.

Frontiers in Oncology, 2024

39703851 (PubMed )
Supplement: DataSheet2.xlsx › Supplemental_data

Molecular profiling and feasibility using a comprehensive hybrid capture panel on a consecutive series of non-small-cell lung cancer patients from a single centre.

Mosteiro M et al.

Esmo Open, 2023

38070435 (PubMed )
Supplement: mmc4.xlsx › Small_variants

DOT1L activity in leukemia cells requires interaction with ubiquitylated H2B that promotes productive nucleosome binding.

Spangler CJ et al.

Cell Reports, 2022

Functional assessment of somatic STK11 variants identified in primary human non-small cell lung cancers.

Donnelly LL et al.

Carcinogenesis, 2021

CDKN2A loss-of-function predicts immunotherapy resistance in non-small cell lung cancer.

Gutiontov SI et al.

Scientific Reports, 2021

34625620 (PubMed )
Supplement: 41598_2021_99524_MOESM2_ESM.xlsx › Mutations

A Distinctive Adnexal (Usually Paratubal) Neoplasm Often Associated With Peutz-Jeghers Syndrome and Characterized by STK11 Alterations (STK11 Adnexal Tumor): A Report of 22 Cases.

Bennett JA et al.

The American Journal of Surgical Pathology, 2021

Deep Sequencing Analysis Reveals That KRAS Mutation Is a Marker of Poor Prognosis in Patients with Pulmonary Sarcomatoid Carcinoma.

Lococo F et al.

Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer, 2016

Genetic and Clinical Analyses of Southern Chinese Children with Peutz-Jeghers Syndrome.

Fu J et al.

Genetic Testing and Molecular Biomarkers, 2015

An unusual case of sex cord tumor with annular tubules with malignant transformation in a patient with Peutz-Jeghers syndrome.

Barker D et al.

International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists, 2010

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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."