Genetic Mutations Course
Gain expertise in colorectal cancer genetic mutations, including APC, KRAS, TP53, and MMR variants. Master interpretation of variants and VUS, integration of tumour and germline testing data, use of genomic databases, and creation of clear reports to guide oncology decisions and research.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This course provides 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 tumor and germline data, utilise major variant databases, and produce actionable reports for therapy selection and clinical decisions.
Elevify advantages
Develop skills
- Interpret cancer variants confidently, classifying missense, truncating, and VUS.
- Analyse colorectal cancer pathways, linking APC, KRAS, TP53, MMR changes to disease.
- Utilise tumour and germline tests like MSI, IHC, sequencing to clarify mutation status.
- Access genomic databases such as COSMIC, ClinVar, cBioPortal, gnomAD for variant annotation.
- Convert genetic findings into actionable reports for oncology teams.
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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