types of mutation

Cards (15)

  • Mutation
    A change that occurs in our DNA sequence, either due to mistakes when DNA is copied or as the result of environmental factors such as UV light
  • DNA sequence of a gene
    • Can be altered in a number of ways
  • Gene mutations

    Have varying effects on health, depending on where they occur and whether they alter the function of essential proteins
  • Types of Mutation

    • Gene Mutation
    • Chromosome Mutation
  • Point mutation or substitution

    A genetic mutation where a single nucleotide base is changed, inserted or deleted from a sequence of DNA or RNA
  • Silent mutations

    Mutations in DNA that do not have an observable effect on the organism's phenotype. They are a specific type of neutral mutation.
  • Nonsense mutation

    A change in one DNA base pair that prematurely signals the cell to stop building a protein, resulting in a shortened protein that may function improperly or not at all
  • Missense mutation

    A change in one DNA base pair that results in the substitution of one amino acid for another in the protein made by a gene
  • Frameshift mutation

    A change in which the addition or loss of DNA bases changes a gene's reading frame, shifting the grouping of these bases and changing the code for amino acids, resulting in a usually nonfunctional protein
  • Deletion
    A change that removes a piece of DNA, which may alter the function of the resulting protein(s)
  • Insertion
    A change that adds a piece of DNA to a gene, causing the protein made by the gene to not function properly
  • Chromosome mutation

    An unpredictable change that occurs in a chromosome, often brought on by problems during meiosis or by mutagens
  • Inversion
    A mutation in which a portion of a genetic material or a chromosome is rotated 180 degrees before rejoining
  • Translocation
    A mutation in which a portion of a chromosome is relocated, either to a different position on the same chromosome or to a different chromosome
  • Duplication
    A mutation in which a portion of a genetic material or a chromosome is duplicated or replicated, resulting in multiple copies of that region