Primary, secondary, and tertiary structures would be altered in a frameshift mutation.
What is frameshift mutation?
- A genetic mutation known as a frameshift mutation, also known as a framing error or reading frame shift, is brought on by indels (insertions or deletions) of many nucleotides in a DNA sequence that is not divisible by three.
- The insertion or deletion might alter the reading frame (the grouping of the codons) because of the triplet nature of gene expression via codons, which leads to a completely different translation from the original.
- The protein is more changed the earlier in the sequence the deletion or insertion takes place.
- A single-nucleotide polymorphism, in which a nucleotide is substituted rather than added or subtracted, is not the same as a frameshift mutation.
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