Abstract:DNA is a remarkably precise medium for copying and storing biological information.
It serves as a design for cellular machinery that permits cells, organs, and even
whole organisms to work. The fidelity of DNA replication results from the action of hundreds
of genes involved in proofreading and damage repair. All human cells can acquire
genetic changes in their DNA all over life. Genetic mutations are changes to the DNA sequence
that happen during cell division when the cells make copies of themselves. Mutations
in the DNA can cause genetic illnesses such as cancer, or they could help humans
better adapt to their environment over time. The endogenous reactive metabolites, therapeutic
medicines, and an excess of environmental mutagens, such as UV rays all continuously
damage DNA, compromising its integrity. One or more chromosomal alterations
and point mutations at a single site (monogenic mutation) including deletions, duplications,
and inversions illustrate such DNA mutations. Genetic conditions can occur when
an altered gene is inherited from parents, which increases the risk of developing that particular
condition, or some gene alterations can happen randomly. Moreover, symptoms of
genetic conditions depend on which gene has a mutation. There are many different diseases
and conditions caused by mutations. Some of the most common genetic conditions
are Alzheimer’s disease, some cancers, cystic fibrosis, Down syndrome, and sickle cell
disease. Interestingly, scientists find that DNA mutations are more common than formerly
thought. This review outlines the main DNA mutations that occur along the human genome
and their influence on human health. The subject of patents pertaining to DNA mutations
and genetic disorders has been brought up.