What is another word for Frameshift Mutation?
Pronunciation: [fɹˈe͡ɪmʃɪft mjuːtˈe͡ɪʃən] (IPA) 
Frameshift mutation is a kind of genetic variation that occurs when one or more nucleotides are added or deleted in DNA sequences. This genetic change can have detrimental effects on gene expression and protein production. There are a variety of synonyms that are used to describe this type of mutation, such as reading frame shift, reading frame mutation, nucleotide shift, codon deletion, and codon insertion. Other terms that are sometimes used include indel mutations, insertions and deletions, and shift mutations. No matter what terminology is used, frameshift mutations are important to understand because they can have serious impacts on human health, and the study of these mutations is essential for the development of medical treatments and therapies.
