The answer is inversion.
What is meant by FRAME-SHIFT MUTATION?
- A frameshift mutation is a type of gene mutation where the addition or deletion of one or more nucleotides results in a shift in the reading frame of the codons in the messenger RNA, which may cause the amino acid sequence to change during protein translation.
- A frame-shift mutation is a type of mutation that alters how the genetic code reads a nucleic acid sequence.
- There are two main ways frame-shift mutation can happen: deletion and insertion.
- When a nucleotide base is deleted from the sequence, a mutation occurs, whereas a mutation occurs when a nucleotide base is inserted.
- DNA's nucleotide sequence can change as a result of deletion and insertion. Inversion is the kind of mutation that isn't a frame-shift mutation, so to speak.
The type of mutation that is not a type of frame-shift mutation is inversion.
To learn more about frame-shift mutation, refer to:
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