In chromatin, substitution mutations are most common in linker regions. Option d is the correct answer.
Mutation by substitution When one nucleotide base is replaced by another, this occurs. Mismatch mutation A type of substitution mutation in which a single nucleotide is replaced, resulting in the coding of an incorrect amino acid, which usually results in a malfunctioning protein. Silent mutations are the result of genetic code redundancy (degeneracy): This is false, as silent mutations are the result of a base substitution that has no discernible effect on a protein's amino acid sequence.
Learn motre more about subsitution here:
brainly.com/question/29383142
#SPJ4
A. enough statistical support for the research hypothesis when there is not
C- the cell is preforming mitosis
Answer:
c
Explanation:
heart is located slightly behind the sternum (chest bone)
