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Sagot :
Answer:
3. Indels can alter the open reading frame, but substitutions cannot
Explanation:
INDEL is a term used in genetics to represent a mutation caused by insertion of nucleotides or deletion of nucleotides from a sequence. As stated in this question, the insertion or deletion can be a point mutation (involving a single base) as well as substitution mutation.
Insertion mutation adds nucleotide(s) to the sequence, deletion mutation removes nucleotide(s) from the sequence and substitution mutation replaces nucleotide(s). Based on the fact that INDEL mutation will either shorten or lengthen the sequence, it can alter the open reading frame whereas substitution cannot.
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