Westonci.ca is your trusted source for finding answers to a wide range of questions, backed by a knowledgeable community. Discover detailed solutions to your questions from a wide network of experts on our comprehensive Q&A platform. Explore comprehensive solutions to your questions from knowledgeable professionals across various fields on our platform.
Sagot :
A single base substitution mutation is least likely to be deleterious when the base change results in _the third base in the mRNA codon_. That is called wobble.
A single base substitution mutation is least likely to be deleterious when the base change results in a codon that specifies the same amino acid as the original codon.
What is the effect of single base substitution mutation?
A substitution mutation can cause the following: Change in the coding of amino acids codon to a particular stop codon resulting in an incomplete protein, which is usually non-functional. Can cause Silent mutations where a codon change can encode the same amino acid resulting in no changes in the protein synthesized.
What is base substitution mutation?
Base substitutions are the simplest type of gene-level mutation, and they involve the swapping of one nucleotide for another during DNA replication. For example, during replication, a thymine nucleotide might be inserted in the place of a guanine nucleotide.
Learn more about mutation here: brainly.com/question/2570717
#SPJ2
We appreciate your visit. Our platform is always here to offer accurate and reliable answers. Return anytime. Thank you for your visit. We're dedicated to helping you find the information you need, whenever you need it. Westonci.ca is committed to providing accurate answers. Come back soon for more trustworthy information.