Final answer:
A deletion mutation with two fewer nucleotides can result in a frameshift mutation, leading to significant changes in the amino acid sequence and protein function.
Explanation:
Identification of mutation: The mutation that caused the difference in the protein can be identified as a deletion since there are two fewer nucleotides in the sequence compared to the original.
Effect on amino acid sequence: A deletion mutation can lead to a frameshift mutation, altering the reading frame and potentially resulting in a completely different amino acid sequence, affecting the protein's function.
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