Genetic Mutations Course
Gain mastery over essential genetic mutations in colorectal cancer. The course teaches interpretation of APC, KRAS, TP53, and MMR variants, resolution of VUS, integration of tumour and germline data, and conversion of complex genomic results into straightforward, actionable reports for clinical practice and research purposes. Participants develop skills to confidently classify variants, analyse cancer pathways, apply testing methods like MSI and IHC, leverage databases such as COSMIC and ClinVar, and communicate findings effectively to oncology teams.

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. Participants will learn to interpret missense, truncating, and VUS findings, integrate tumour and germline data, utilise major variant databases, and produce clear, actionable reports to guide therapy selection and clinical decisions.
Elevify advantages
Develop skills
- Interpret cancer variants by confidently classifying missense, truncating, and VUS findings.
- Analyse colorectal cancer pathways, linking APC, KRAS, TP53, and MMR alterations to disease progression.
- Utilise tumour and germline testing, 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 mutations into patient 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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