Point mutations are defined as a single modification or alteration in the nucleotide base of the cell's genetic code. It might be a single nucleotide base that is deleted, added, or inverted.
The mutations that took place are 1. C and 2. B in the list below.
How can the mutation be accounted for?
A single base's triplet codon experiences a silent mutation, but the changes are neutral and do not affect the base's ability to function. They have no impact on how the protein works. Therefore, the silent mutation from glycine to glycine.
When a single nucleotide base change results in the stop codon being formed, this is known as a non-sense mutation.
As a result, the lysine to stop codon mutation is nonsensical.
As a result, nonsense and silent mutations are the best choices.
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