Genetic Mutations Course
Dive into essential genetic mutations driving colorectal cancer. Master interpretation of APC, KRAS, TP53, and MMR variants, resolve variants of uncertain significance, integrate tumour and germline testing data, and create actionable reports to inform clinical decisions and research in oncology.

4 to 360 hours 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. Gain skills to interpret missense, truncating, and VUS results, integrate tumour and germline data, utilise major variant databases, and produce clear reports that guide therapy and clinical decisions.
Elevify advantages
Develop skills
- Interpret cancer variants confidently, classifying missense, truncating, and VUS accurately.
- Analyse colorectal cancer pathways, connecting APC, KRAS, TP53, and MMR alterations to disease progression.
- Utilise tumour and germline tests like MSI, IHC, and sequencing to clarify mutation status.
- Access genomic databases such as COSMIC, ClinVar, cBioPortal, and gnomAD for variant annotation.
- Translate genetic findings into concise, 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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