<u>Substituion mutation</u> is responsible for small changes in a trait.
Explanation:
This kind of mutation merely changes the type of nucleotide in the DNA sequence. The mutation does not cause a frameshift as would a deletion of addition mutation.
A substitution mutation would at worst change an amino acid in the translated protein. This would likely have a slight effect on how the protein folds into an active protein. On the other hand, mutations that cause frameshifts have the biggest effect on the proteins. They change all the amino acids of a protein downstream of the point of mutation.
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RNA editing terminal uridylyl transferase, aKa. TUTase 2, aka. RET 2
__Rain Forest___Novanet__
Answer: A or C
B would not make sense, and no cell can mock a mitochondria
It would most likely be A
