This document discusses frameshift mutations. It begins by defining frameshift mutations as insertions or deletions in DNA that are not in multiples of three nucleotides, causing a shift in the reading frame. It then describes the mechanisms of deletion and insertion mutations and their effects, including producing non-functional proteins. Examples are given of sense, missense, and nonsense codons produced by frameshifts. Applications in molecular therapy and targeting cancer proteins are mentioned. The conclusion summarizes that frameshifts can occur via insertion or deletion, may lead to changes in polypeptide length and composition, and have been associated with various diseases.