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29 November, 02:34

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

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  1. 29 November, 02:56
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    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.
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