Answer:
1. silent mutation
2. non sense mutation
3. missense mutation
Explanation:
1. in a silent mutation, the substituted base will code for another codon that will get translated to the same amnio acid
2. in a non sense mutation, the substituted base will code for a STOP codon that would cause the production of a faulty, usually non functional protein, missing some amnio acids.
3. in a missense mutation, the substituted codon codes for a different amino acid and this can have a small to great effect on the product protein based on its function. eg: sickle cell anemia where you've substituted a polar amino acid with a non polar one, thus causing severe consequences
