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This deck focuses on Mutations, giving you a quick way to review the definitions, rules, and examples that matter most for AP Biology.
Study Mutations in AP Biology with focused flashcards that help you recognize the idea, recall the key rule, and apply it in practice-style prompts.
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What is induced mutation?
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A mutation caused by environmental factors. Results from exposure to mutagens in the environment.
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This deck focuses on Mutations, giving you a quick way to review the definitions, rules, and examples that matter most for AP Biology.
Work through these flashcards in short sessions. Try to answer each prompt before flipping the card, then revisit any cards you miss until the explanation feels automatic.
Answer: A mutation caused by environmental factors. Results from exposure to mutagens in the environment.
Answer: A deletion mutation. One nucleotide (T) was removed, shortening the sequence.
Answer: A mutation that reverses the effect of a previous mutation. Restores original gene function through reversion.
Answer: A mutation with no effect on an organism's fitness. Does not affect survival or reproductive success.
Answer: A mutation that expresses under certain conditions. Temperature-sensitive or other environmental triggers.
Answer: A mutation that introduces a premature stop codon. Truncates protein synthesis early, often disrupting function.
Answer: A mutation that occurs without external influence. Arises from normal cellular processes like DNA replication errors.
Answer: Nonsense mutation. Creates premature termination of protein synthesis.
Answer: A mutation that provides a survival benefit. Improves fitness and may be selected for.
Answer: A mutation that introduces a premature stop codon. Truncates protein synthesis early, often disrupting function.
Answer: A mutation that reverses the effect of a previous mutation. Restores original gene function through reversion.
Answer: A mutation that results in the death of the organism. Severely impairs organism survival or reproduction.
Answer: A mutation that does not change the amino acid sequence. Due to genetic code degeneracy, same amino acid encoded.
Answer: A mutation where chromosome segments are rearranged. Moves genetic material between different chromosomes.
Answer: A change in the nucleotide sequence of DNA. The fundamental alteration that can affect gene function.
Answer: Transversion mutation. Purine to pyrimidine or pyrimidine to purine substitution.
Answer: A change in the nucleotide sequence of DNA. The fundamental alteration that can affect gene function.
Answer: Silent mutation. Synonymous substitution maintains protein sequence.
Answer: A mutation where chromosome segments are rearranged. Moves genetic material between different chromosomes.
Answer: Deletion mutation. Loss of genetic material and associated genes.
Answer: Increased tendency of genome to acquire mutations. Defective DNA repair leads to mutation accumulation.
Answer: Deletion mutation. Loss of genetic material and associated genes.
Answer: Translocation mutation. Segments move from one chromosome to another.
Answer: Translocation mutation. Segments move from one chromosome to another.
Answer: Silent mutation. Genetic code degeneracy allows same amino acid coding.
Answer: A mutation that occurs without external influence. Arises from normal cellular processes like DNA replication errors.
Answer: An insertion mutation. An extra C was added between positions 3 and 4.
Answer: Duplication mutation. Creates extra copies of genes in that segment.
Answer: A silent mutation. Both codons encode lysine due to genetic code redundancy.
Answer: Silent mutation. Synonymous substitution maintains protein sequence.
Answer: A mutation that results in a different amino acid. Changes protein structure by altering amino acid sequence.
Answer: A mutation with no effect on an organism's fitness. Does not affect survival or reproductive success.
Answer: A mutation that results in a different amino acid. Changes protein structure by altering amino acid sequence.
Answer: A permanent alteration in the DNA sequence. Cannot be reversed and passes to offspring if in gametes.
Answer: A mutation where a chromosome segment is reversed. Gene order is flipped but all genes remain present.
Answer: Transition mutation. Same chemical class substitution (purine-purine or pyrimidine-pyrimidine).
Answer: A mutation that results in the death of the organism. Severely impairs organism survival or reproduction.
Answer: A mutation that results in multiple copies of a gene. Can lead to gene dosage effects and imbalances.
Answer: An insertion mutation. An extra C was added between positions 3 and 4.
Answer: A silent mutation. Both codons encode lysine due to genetic code redundancy.
Answer: A permanent alteration in the DNA sequence. Cannot be reversed and passes to offspring if in gametes.
Answer: Frameshift mutation. Insertion disrupts reading frame, altering all downstream codons.
Answer: Nonsense mutation. Creates premature termination of protein synthesis.
Answer: A gene that protects a cell from one step on the path to cancer. Prevents cancer by regulating cell division.
Answer: Missense mutation. Point mutation that alters the encoded amino acid.
Answer: A transversion mutation. T (pyrimidine) to G (purine) is purine-pyrimidine switch.
Answer: Aneuploidy. Abnormal chromosome number disrupts gene dosage.
Answer: Duplication mutation. Creates extra copies of genes in that segment.
Answer: An agent that induces mutations in DNA. External factors that increase mutation rates.
Answer: A mutation that shifts the reading frame of codons. Insertions or deletions shift all downstream codons.
Answer: A transversion mutation. T (pyrimidine) to G (purine) is purine-pyrimidine switch.
Answer: Altered reading frame leading to incorrect protein synthesis. Disrupts triplet codon reading pattern downstream.
Answer: A mutation that shifts the reading frame of codons. Insertions or deletions shift all downstream codons.
Answer: A deletion mutation. One nucleotide (T) was removed, shortening the sequence.
Answer: A disease resulting from gene mutations. Mutations disrupt normal gene function causing illness.
Answer: Transition mutation. Same chemical class substitution (purine-purine or pyrimidine-pyrimidine).
Answer: A mutation that provides a survival benefit. Improves fitness and may be selected for.
Answer: A mutation where a chromosome segment is reversed. Gene order is flipped but all genes remain present.
Answer: A mutation that affects the structure of chromosomes. Large-scale changes involving chromosome structure.
Answer: A mutation that affects the structure of chromosomes. Large-scale changes involving chromosome structure.
Answer: A mutation that results in multiple copies of a gene. Can lead to gene dosage effects and imbalances.
Answer: A mutation that does not change the amino acid sequence. Due to genetic code degeneracy, same amino acid encoded.
Answer: A mutation caused by environmental factors. Results from exposure to mutagens in the environment.
Answer: An agent that induces mutations in DNA. External factors that increase mutation rates.
Answer: A disease resulting from gene mutations. Mutations disrupt normal gene function causing illness.
Answer: A mutation that expresses under certain conditions. Temperature-sensitive or other environmental triggers.
Answer: Silent mutation. Genetic code degeneracy allows same amino acid coding.
Answer: Frameshift mutation. Insertion disrupts reading frame, altering all downstream codons.
Answer: Missense mutation. Point mutation that alters the encoded amino acid.