Genetic Mutations Course
Dive into the genetics of colorectal cancer with this focused course. Master interpretation of mutations in genes like APC, KRAS, TP53, and MMR, resolve variants of uncertain significance (VUS), integrate tumor and germline testing results, leverage genomic databases, and create clear reports that inform oncology care and research decisions. Ideal for clinicians and researchers seeking practical genetic skills.

4 to 360h flexible workload
certificate valid in your country
What will I learn?
This course provides a practical overview of colorectal cancer genetics, covering key pathways, driver genes, variant types, and clinical relevance. Participants will learn to interpret missense, truncating, and VUS findings, integrate tumor and germline data, utilize major variant databases, and produce actionable reports to guide therapy selection and clinical decisions.
Elevify advantages
Develop skills
- Interpret cancer variants confidently, classifying missense, truncating, and VUS accurately.
- 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 and apply genomic databases like COSMIC, ClinVar, cBioPortal, and gnomAD for variant annotation.
- Translate genetic findings into actionable reports for oncology teams and clinical decision-making.
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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