The mutation in the provided DNA sequences can be categorized as a substitution mutation.
Here's the breakdown:
- In the original sequence, the nucleotide "C" in the first strand of the second position is changed to "A" in the mutated sequence.
- Similarly, in the complementary strand, the nucleotide "G" in the position corresponding to the first position of the mutated strand is changed to "T".
Since one base in the sequence is replaced by another without the addition or removal of bases, this is a substitution mutation.