Answer:
Step-by-step explanation:
1.A deletion mutation occurs when a wrinkle forms on the DNA template strand and subsequently causes a nucleotide to be omitted from the replicated strand.
2.This type of variant results in a shortened protein that may function improperly, be nonfunctional, or get broken down. An insertion changes the DNA sequence by adding one or more nucleotides to the gene.
3. A substitution mutation can cause the following: Change in the coding of amino acids codon to a particular stop codon resulting in an incomplete protein, which is usually non-functional. Can cause Silent mutations where a codon change can encode the same amino acid resulting in no changes in the protein synthesized.
4. when a premature nonsense or stop codon is introduced in the DNA sequence. When the mutated sequence is translated into a protein, the resulting protein is incomplete and shorter than normal. Consequently, most nonsense mutations result in nonfunctional proteins.