Types of Mutations & Mutational Effects

20 questions β€’ 1 test β€’ tap a section to begin

Welcome! 4.4 Types of Mutations & Mutational Effects β€” Test 2 — 20 questions, CSIR-NET style.

What this test covers

  • Point mutations: transitions, transversions
  • Nonsense, missense, silent & frameshift effects
  • Spontaneous vs germline/somatic vs conditional
  • Hot spots, Haldane's rule & nonsense suppression

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4.4 Types of Mutations & Mutational Effects β€” Test 2
Q1. A mutation involving the change of a single base pair in DNA is a:βœ“ Point mutation
Q2. Which of the following is a transversion mutation?βœ“ C to A
Q3. A transition mutation is exemplified by the change:βœ“ G to A
Q4. Changing the codon UGC to UGA represents which type of mutation?βœ“ Nonsense
Q5. The main consequence of a frameshift mutation is that it:βœ“ Alters the reading frame, changing all downstream amino acids
Q6. A site on DNA that shows an unusually high rate of mutation is called a:βœ“ Hot spot
Q7. A spontaneous mutation usually originates as an error in:βœ“ DNA replication
Q8. A tautomeric shift of a nitrogenous base typically causes a:βœ“ Spontaneous mutation
Q9. Germinal (germline) mutations originate during ___ , whereas somatic mutations originate during ___ :βœ“ meiosis; mitosis
Q10. A mutation that affects the phenotype only under certain conditions (e.g. temperature) is a:βœ“ Conditional mutation
Q11. A mutation that is intentionally introduced at a defined position is called:βœ“ A site-directed mutation
Q12. Mutations are biologically important because they can provide:βœ“ Genetic variation for evolution and adaptation
Q13. Point mutations can arise from:βœ“ Any of these
Q14. The codon for leucine is CUC. How many different amino acids could result from single-base substitutions of this codon?βœ“ 7
Q15. Gene (point) mutations include which of the following changes?βœ“ Substitution, insertion and deletion of bases
Q16. In an X-linked recessive lethal disorder, what fraction of cases (by Haldane's rule) is expected to arise from new mutations?βœ“ About 33% (one third)
Q17. Retinoblastoma in a child with no family history is often the result of a:βœ“ Somatic mutation (plus an inherited or second somatic hit)
Q18. A gain-of-function mutation that drives increased cell proliferation and can lead to cancer typically converts a proto-oncogene into a(n):βœ“ Oncogene
Q19. A truncated protein results from a nonsense mutation. A second mutation that could restore a full-length protein would best be introduced in a:βœ“ Transfer-RNA (tRNA) gene
Q20. Match each mutation type with its description and select the correct option.βœ“ A-ii, B-i, C-iv, D-iii