Final answer:
In scenario A, substituting thymine for the sixth nucleotide is a transition leading to a missense mutation. Scenario B, a transition at the eleventh nucleotide, typically results in a silent mutation. Scenario C, a transversion at the fifteenth nucleotide, results in a missense mutation.
Step-by-step explanation:
For scenario A, where a thymine is substituted for nucleotide 6, the original sequence would be G so replacing it with a T would be a transition mutation. This changes the amino acid coded by this codon, resulting in a missense mutation.
In scenario B, a guanine substituted for nucleotide 11, would also be a transition, because the original base is C and it's replaced with G, which does not change the amino acid due to the redundancy of the genetic code (silent mutation not listed as an option). Scenario C, a guanine replacing nucleotide 15 that originally was an A, is a transversion. Since this changes the resulting amino acid, it's considered a missense mutation.