Genetic Mutations Course
Gain mastery over genetic mutations in colorectal cancer through this focused course. Explore APC, KRAS, TP53, and MMR variants, resolve uncertainties like VUS, integrate tumor and germline testing data, leverage genomic databases, and create clear reports to guide clinical and research decisions effectively.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This course offers a practical overview of colorectal cancer genetics, covering key pathways, driver genes, variant types, and clinical relevance. You will learn to interpret missense, truncating, and VUS results, integrate tumor and germline data, utilize major variant databases, and produce actionable reports for therapy selection and clinical decisions.
Elevify advantages
Develop skills
- Interpret cancer variants confidently by classifying missense, truncating, and VUS findings.
- Analyze colorectal cancer pathways linking APC, KRAS, TP53, and MMR alterations to disease progression.
- Utilize tumor and germline tests including MSI, IHC, and sequencing to determine mutation status.
- Access genomic databases like COSMIC, ClinVar, cBioPortal, and gnomAD for variant annotation.
- Convert genetic mutations into practical care through clear, actionable reports for oncology teams.
Suggested summary
Before starting, you can change the chapters and the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.What our students say
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