CAIE IGCSE Biology 18.1.6 Mutation as Genetic Change
Practise defining mutation as genetic change and recognising changes to DNA base sequence in unfamiliar contexts.
- Syllabus
- 2026–2028
- Course
- Biology 0610
Practise defining mutation as genetic change and recognising changes to DNA base sequence in unfamiliar contexts.
Colour blindness is a characteristic that is inherited. Colour blindness is more common in males than in females.
Fig. 6.1 is a pedigree diagram showing the inheritance of colour blindness in a family.

Fig. 6.1
There was no history of colour blindness in the parents and grandparents of individuals 1 and 2.
Suggest how colour blindness first occurred in the family in Fig. 6.1.
any two from:
mutation ;
to give, recessive allele / b ;
occurred in 3 or in one of her parents / 1 or 2 or her grandparents ;
AVP ; e.g. other reason such as donated gamete