Final answer:
A point mutation changes a single nucleotide base in DNA and can result in silent, missense, or nonsense mutations. While a silent mutation does not typically alter protein function, missense and nonsense mutations can have significant effects if they occur in critical regions of the protein.
Step-by-step explanation:
When considering how likely a point mutation is to cause a change in the amino acid sequence of a protein, several factors come into play. A point mutation refers to the alteration of a single nucleotide base in the DNA, which may result in a silent, missense, or nonsense mutation.
A silent mutation generally does not affect the amino acid sequence due to the redundancy of the genetic code. However, a missense mutation leads to the incorporation of a different amino acid, and this can vary in impact depending on the chemical properties and the role of the new amino acid within the protein. A nonsense mutation, on the other hand, transforms a sense codon into a stop codon, potentially leading to truncated, often non-functional proteins.
Considering the genetic degeneracy, many point mutations may be silent and thus do not affect the protein's functionality. However, if a missense or nonsense mutation occurs, particularly in a crucial region of the protein such as the active site, the consequences can be significant and potentially deleterious, as seen in disorders like sickle-cell disease.