Genetic Mutations Course
Gain mastery over 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 actionable reports for clinical practice and research purposes. It equips learners with skills to confidently classify variants and support oncology decisions using databases like COSMIC and ClinVar.

from 4 to 360h flexible workload
certificate valid 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, 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 mutations into clinical 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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