Deletion Mutation

A deletion mutation occurs when a section of genetic code is missing or deleted. This type of mutation can affect the health of the individual, and in some cases, may lead to a genetic disorder or disease. It can also cause a change in the phenotype of the organism, leading to physical differences between the affected individual and their family members. Deletion mutation is important for understanding genetic disorders and for the development of treatments for genetic diseases. It can also help to predict the risk of future genetic health issues for individuals and their families.