The position within the original arginine codon where the point mutation most likely occurred was the second nucleotide. In this case, the mutation was CGA >> CAA.
<h3>Mutations and codons</h3>
A mutation is any alteration in the nucleotide sequence of an organism.
A point mutation is a single base substitution that doesn't change the open reading frame of a given protein.
In this case, the CGA codon encodes for Arginine, whereas the CAA codon encodes for Glutamine, thereby the mutation likely occurred in the second base (C<u>G</u>A >> C<u>A</u>A)
Learn more about mutation here:
brainly.com/question/17031191
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23 haploid Chromosomes for each human
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