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Any alteration to DNA that can potentially result in a change in the function of one or more genes. Mutations can be a change in a single base of DNA (point mutation) or a loss of base pairs (deletion) affecting a single gene, or a movement of chromosomal regions (translocation) affecting many genes. Mutations can be induced by radiation, chemical treatment, foreign pathogens (e.g. viruses), or due to errors that occur during replication of the genome each time a cell divides. Mutations can affect gene regulation and expression or can cause a change in the protein itself that results in a non-functional protein (e.g. the CFTR protein defective in cystic fibrosis) or one with abnormal activity (e.g. the p53 cancer-causing protein). Some changes in DNA occur naturally and lead to no harmful effects; these changes in a population are called polymorphisms.