Types of Mutations

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11 Terms

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mutations

heritable changes in genetic information

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point mutations

mutations that involve changes in one or a few nucleotides (bases); include substitutions, insertions, and deletions

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substitutions

one base is changed to a different base

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deletions

point mutations in which one base is deleted from the DNA sequence

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insertions

point mutations in which one base is inserted into the DNA sequence

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frameshift mutations

cause a shift in the reading frame of the genetic message; can alter the protein tremendously; examples: insertion and deletion

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chromosomal mutations

a change in the number or structure of an entire chromosome; includes deletions, duplications, inversions, and translocations

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deletion (chromosomal)

loss of all or part of a chromosome

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duplication

produces an extra copy of all or part of a chromosome

<p>produces an extra copy of all or part of a chromosome</p>
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inversion

reverses the direction of parts of a chromosome

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translocation

occurs when part of one chromosome breaks off and attaches to another

<p>occurs when part of one chromosome breaks off and attaches to another</p>