Determine the type of mutations based on the nucleotide change- indel vs substitution- that occurred in a sequence. Which of the following mutations would lead to a change in the reading frame in translation? Insertion of six Adenins Deletion of the start codon Insertion of CTA Deletion of two Cytocins
Gene Interactions
When the expression of a single trait is influenced by two or more different non-allelic genes, it is termed as genetic interaction. According to Mendel's law of inheritance, each gene functions in its own way and does not depend on the function of another gene, i.e., a single gene controls each of seven characteristics considered, but the complex contribution of many different genes determine many traits of an organism.
Gene Expression
Gene expression is a process by which the instructions present in deoxyribonucleic acid (DNA) are converted into useful molecules such as proteins, and functional messenger ribonucleic (mRNA) molecules in the case of non-protein-coding genes.

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