A mutation is an alteration in the DNA sequence of an organism, virus, or extrachromosomal DNA
. Mutations can occur during DNA or viral replication, mitosis, or meiosis and may result from exposure to mutagens or viral infection
. A mutation can be passed to offspring if it occurs in germline cells (eggs and sperm) but not if it occurs in somatic cells (body cells)
. Mutations are a main cause of diversity among organisms
. Mutations can be changes within genes, called point mutations, or mutations that span more than one gene, called chromosomal mutations
. Types of mutations:
- Point Mutations Point mutations are changes to single base pairs and may substitute an incorrect amino acid in the corresponding position in the encoded protein
- Chromosomal Mutations Chromosomal mutations affect the structure, function, and inheritance of entire DNA molecules
. Examples include large-scale deletions, duplications, inversions, and translocations. Inversions and translocations are functionally normal unless a break occurs within a gene.
- Substitution Substitutions exchange one base for another
- Nonsynonymous Mutation These mutations lead to either the production of a different protein or the premature termination of a protein
- Synonymous Mutations Synonymous mutations do not change an amino acid sequence but occur only in sequences that code for amino acids
- Insertion Insertions add one or a few nucleotides
- Deletion Deletions remove one or a few nucleotides