Occasional errors may occur during DNA replication.
Chromosome mutations

In biology, a mutation is a change in the genetic material. This means changes to the DNA or to the chromosomes which carry the DNA. These changes are heritable (can be passed on to the next generation) unless they have lethal effects.

Mutations can happen for several reasons. It can happen because of errors when meiosis produces the gametes (eggs & sperms). Damage by radiation, or by certain chemicals may cause mutations. Mutations occur at random.

Also, by derivation, an individual carrying the mutation may be called a mutant or a mutation. So is the trait (character) most obviously affected by the mutation.[1]

Types of mutation

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Gene duplication causes different lengths at a single locus (allele). Shows variation in one gene in six individuals.

DNA mutations

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When DNA is copied mistakes are sometimes made – these are called mutations. There are four main types of mutations:

Chromosome mutations

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These terms are explained in the third diagram.

Results of mutation

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Mutations may be bad for the organism, or neutral, or benefit the organism. Sometimes mutations are fatal for the organism – the protein made by the 'new' DNA does not work at all, and causing the embryo to die. On the other hand, evolution is moved forward by mutations, when the new version of the protein works better for the organism.

Mutations are the ultimate source of variation, upon which natural selection acts. What happens is that some mutations affect the organism's ability to live and reproduce. This is an important part of the theory of evolution. The amount of heritable variation carried by a population can be huge, and as a result natural populations can change and adapt to conditions in their environment.[1]

References

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  1. 1.0 1.1 Maynard Smith, John 1998. Evolutionary genetics, 2nd ed. Oxford. p53–64
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