Mutation

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Last updated 5:58 PM on 2/26/25
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25 Terms

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Point Mutation
A single change in a base in the DNA sequence.
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Single Substitution Mutation

A mutation where one base is swapped for another, changing one amino acid in the protein.
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Insertion Mutation (INDEL)

A type of point mutation where extra bases are added into the DNA sequence.

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Deletion Mutation (INDEL)

A type of point mutation where bases are removed from the DNA.

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Frameshift Mutation
A mutation that occurs from the insertion or deletion of bases, shifting the entire reading frame.
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Duplication Mutation
A mutation involving a section of DNA being copied and repeated.
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Inversion Mutation
A mutation where a section of DNA is flipped around.
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Null Mutation
A mutation that completely breaks a gene, rendering it non-functional.
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Knockdown
A mutation that reduces the gene's activity but does not completely eliminate it.
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Knockout
A mutation that completely removes or inactivates a gene.
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Conservative Mutation

A type of missense mutation that changes the amino acid but does not significantly affect the protein (polar to polar).

<p>A type of missense mutation that changes the amino acid but does not significantly affect the protein (polar to polar).</p>
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Non-Conservative Mutation

A type of misses mutation that changes the amino acid from polar to non polar vise versa

<p>A type of misses mutation that changes the amino acid from polar to non polar vise versa</p>
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Loss of Function Mutation
A mutation that results in the gene or protein stopping its function, which can lead to various diseases.
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Somatic Mutation

A mutation that occurs in non-germline cells and is not inherited, often affecting only the individual organism. (Body cells)

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Germ-line Mutation

A mutation that occurs in the germ cells (sperm and eggs) and can be passed on to offspring, potentially affecting future generations.

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Transversion Mutation

A type of point mutation (Single base Substitution) where a purine is replaced by a pyrimidine or vice versa, leading to changes in DNA sequence.

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Transition Mutation

A type of point mutation (Single Base Substitution) where a purine is substituted for another purine or a pyrimidine for another pyrimidine, resulting in a change in the DNA sequence.

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Silent Mutation

A mutation that doesn’t effect normal, cannot tell there is a mutation (NONE in everything) same genetic code!

<p>A mutation that doesn’t effect normal, cannot tell there is a mutation (NONE in everything) same genetic code! </p>
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Deleterious Mutation

A mutation that is harmful to an organism, often resulting in reduced fitness or negative effects on survival and reproduction.

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Beneficial Mutation

A mutation that enhances an organism's fitness, leading to improved survival or reproduction in a specific environment.

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Neutral Mutation

A mutation that has no significant effect on the organism's fitness, neither beneficial nor harmful.

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Nonsense Mutation

a DNA change that causes a protein to stop being made early

<p><span>a DNA change that causes a protein to stop being made early</span></p>
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Missense Mutation

type of point mutation (Single base substitution) in which a single nucleotide change in a DNA sequence results in the substitution of one amino acid for another in the protein produced.

<p>type of <strong>point mutation</strong> (Single base substitution) in which a single nucleotide change in a DNA sequence results in the substitution of one amino acid for another in the protein produced.</p>
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A, G

PURINE

<p>PURINE</p>
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C, T, U

PYRIMIDINE

<p>PYRIMIDINE </p>

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