TytoAlba95
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I got this question in an exam. Why do silent mutations always affect the third position of a codon? I have no clue about it.
The discussion revolves around the nature of silent mutations in genetic coding, specifically addressing why they are often associated with changes in the third position of a codon. Participants explore the implications of these mutations in the context of translation and codon recognition.
Participants express differing views on whether silent mutations exclusively affect the third position, with some agreeing that they are more common there while others assert that this is not a strict rule. The discussion remains unresolved regarding the absolute nature of silent mutations.
Participants acknowledge a need for further research and clarification on the mechanisms of codon recognition and the implications of silent mutations.
SanjuktaGhosh said:I got this question in an exam. Why do silent mutations always affect the third position of a codon? I have no clue about it.
Because the first two bases are necessary to specify the type of amino acid to be encoded. And they are both the same base. It wouldn't be silent if it was one of the first two bases because then it would be deleterious. Only the third base can change and you can still encode the same amino acid.SanjuktaGhosh said:I got this question in an exam. Why do silent mutations always affect the third position of a codon? I have no clue about it.