Respuesta :
Answer : The correct answer is -
Insertion mutation.
An insertion mutation can be described as a permanent change in the genetic material (DNA sequence) due to the addition of one or more nucleotides. It can result in alteration of protein (due to the change in the reading frame of DNA) , which may cause diseased condition.
In the given question, there is addition/insertion of T (thymine) at the second place in the original DNA sequence-
Original DNA sequence -
ACGTTCATT
Mutated DNA sequence - ATCGTTCATT
Thus, it is an insertion mutation.