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 testing data, and conversion of complex genomic findings into straightforward, actionable reports for clinical practice and research purposes. It equips you with skills to support precise oncology decisions using tools like MSI, IHC, sequencing, and databases such as COSMIC, ClinVar, cBioPortal, and gnomAD.

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. You will learn to interpret missense, truncating, and VUS results, combine tumour and germline data, utilise major variant databases, and produce clear reports that guide therapy choices and clinical decisions.
Elevify advantages
Develop skills
- Interpret cancer variants confidently by classifying missense, truncating, and VUS findings.
- Analyse colorectal cancer pathways by connecting APC, KRAS, TP53, and MMR alterations to disease progression.
- Utilise tumour and germline tests including MSI, IHC, and sequencing to determine mutation status accurately.
- Access genomic databases like COSMIC, ClinVar, cBioPortal, and gnomAD for effective variant annotation.
- Convert genetic mutations into practical clinical reports for oncology teams to inform patient care.
Suggested summary
Before starting, you can change the chapters and 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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