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  • Understanding Point Mutations: A Comprehensive Guide
    When one pair of bases is replaced in a gene, it's called a point mutation.

    Here's a breakdown:

    * Point mutation: A change in a single nucleotide within a gene.

    * Base pair: The two complementary nucleotides that bind together in DNA (Adenine with Thymine, or Guanine with Cytosine).

    Types of Point Mutations:

    * Substitution: One base is replaced with another. This can lead to:

    * Silent mutation: The change doesn't alter the amino acid sequence of the protein.

    * Missense mutation: The change results in a different amino acid being incorporated into the protein.

    * Nonsense mutation: The change results in a stop codon, prematurely terminating protein synthesis.

    * Insertion: An extra base is added to the sequence.

    * Deletion: A base is removed from the sequence.

    Point mutations can have a variety of effects on the resulting protein, ranging from no effect to a complete loss of function.

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