Genetic Mutations Course
Gain mastery in interpreting key genetic mutations in colorectal cancer, including APC, KRAS, TP53, and MMR variants. Resolve variants of uncertain significance (VUS), integrate tumour and germline testing data, leverage genomic databases, and generate actionable reports to inform clinical decisions and research applications effectively.

4 to 360 hours flexible workload
valid certificate in your country
What will I learn?
This course offers a focused 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 tumour and germline data, utilise major variant databases, and produce clear reports to guide therapy and clinical decisions.
Elevify advantages
Develop skills
- Interpret cancer variants confidently by classifying missense, truncating, and VUS findings.
- Analyse colorectal cancer pathways, linking APC, KRAS, TP53, and MMR alterations to disease progression.
- Utilise tumour and germline tests including MSI, IHC, and sequencing to determine mutation status.
- Access genomic databases such as COSMIC, ClinVar, cBioPortal, and gnomAD for variant annotation.
- Translate genetic findings into 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
FAQs
Who is Elevify? How does it work?
Do the courses have certificates?
Are the courses free?
What is the course duration?
What are the courses like?
How do the courses work?
What is the duration of the courses?
What is the cost or price of the courses?
What is an EAD or online course and how does it work?
PDF Course