The helicase breaks the hydrogen bonds between the base pairs, once the DNA is open and accessible, one of the strands is then read and used as a template.
Insertion and deletion mutation are opposites to each other, these mutations are more catastrophic as they result in every triplet ‘downstream’ (ocuring after the point of mutation) of the mutation being changed ( as each base is shuffled into a new codon)
As most amino acids can be coded for by several different codons this means that substitution mutations do not necessarily result in a change to the amino acid sequence of the polypeptide.
The polypeptide chain is released and the mRNA-tRNA structure that was built to create the protein breaks down ready to form again when another protein is needed.