Associated Genetic Biomarkers
PIK3C2G Mutation is present in 2.05% of AACR GENIE cases, with cutaneous melanoma, lung adenocarcinoma, colon adenocarcinoma, endometrial endometrioid adenocarcinoma, and melanoma of unknown primary having the greatest prevalence .
PIK3C2G Mutation serves as an inclusion eligibility criterion in 1 clinical trial, of which 1 is open and 0 are closed. Of the trial that contains PIK3C2G Mutation as an inclusion criterion, 1 is phase 1 (1 open).
Trials with PIK3C2G Mutation in the inclusion eligibility criteria most commonly target malignant solid tumor .
Paxalisib and radiation therapy are the most frequent therapies in trials with PIK3C2G Mutation as an inclusion criteria .
Significance of PIK3C2G Mutation in Diseases
Malignant Solid Tumor +
PIK3C2G is altered in 3.27% of malignant solid tumor patients with PIK3C2G Mutation present in 2.22% of all malignant solid tumor patients .
PIK3C2G Mutation is an inclusion criterion in 1 clinical trial for malignant solid tumor, of which 1 is open and 0 are closed. Of the trial that contains PIK3C2G Mutation and malignant solid tumor as inclusion criteria, 1 is phase 1 (1 open) .
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