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Musya8 [376]
4 years ago
13

The most commonly occurring mutation in people with cystic fibrosis is a deletion of a single codon. this mostly likely results

in
Biology
1 answer:
Free_Kalibri [48]4 years ago
6 0

<span>It would result in a polypeptide which has a missing amino acid.  The genetic mutation that occurs in a person with cystic fibrosis is called frameshift mutation which is caused by an insertion or deletion of nucleotides that is not divisible by three in a sequence of DNA.</span>

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