Genetic Mutations Course
Gain mastery over essential genetic mutations in colorectal cancer. The course teaches interpretation of APC, KRAS, TP53, and MMR variants, handling VUS, integrating tumour and germline data, and converting complex findings into straightforward, actionable reports for clinical and research purposes. It equips you with skills for precise genetic analysis in oncology.

flexible workload of 4 to 360h
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, combine tumour and germline data, utilise major variant databases, and produce clear reports to guide therapy and clinical choices.
Elevify advantages
Develop skills
- Interpret cancer variants confidently by classifying missense, truncating, and VUS.
- Analyse colorectal cancer pathways, connecting APC, KRAS, TP53, MMR alterations to disease progression.
- Utilise tumour and germline testing like MSI, IHC, and sequencing to clarify mutation status.
- Access genomic databases such as COSMIC, ClinVar, cBioPortal, gnomAD for variant annotation.
- Convert genetic mutations into practical care plans with clear 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 workloadWhat our students say
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