Which of the following mutations would cause a premature stop codon?

Prepare for the AAB Molecular Diagnostics Test with focused study materials and practice questions. Gain insights into questions, formats, and key topics to excel in your exam and advance your career in molecular diagnostics.

A nonsense mutation is the correct choice because it specifically involves a change in the nucleotide sequence that leads to the creation of a premature stop codon. This occurs when a single nucleotide change in the DNA sequence alters the codon such that it encodes a stop signal instead of an amino acid. As a result, translation of the mRNA is terminated earlier than expected, leading to a truncated protein that is often nonfunctional.

In contrast, a silent mutation does not change the amino acid sequence, as it alters a nucleotide but still codes for the same amino acid due to the redundancy of the genetic code. A missense mutation results in the substitution of one amino acid for another, which may affect protein function but does not result in a premature stop. An insertion mutation typically adds one or more nucleotides into the sequence, which could potentially lead to a frameshift that might create a premature stop codon, but it does not guarantee this outcome in every case. Thus, a nonsense mutation directly leads to premature termination of protein synthesis, making it the most relevant answer here.

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