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.
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DNA is made of a double helix of two complementary strands. When replicating, these strands seperate. Each strand of the original DNA then acts as a template for the production of it's counterpart, which is referred to as semiconservative replication.
Fungus uses its hyphae to obtain nutrients.
A) sulfide mineral: Contain sulfur plus a metallic element
B) sulfate mineral: Compounds that have a sulfur atom surrounded by four oxygen atoms
C) halide minerals: Contain elements like fluorine, bromine, iodine, or chlorine combined with metals. Stable salt is an example of this type of mineral
D) carbonate mineral: Compounds made up of a carbon atom that is bordered by three oxygen atoms.
The appropriate response is lipid bilayer. The lipid bilayer is a widespread segment of all cell films. Its part is basic since its basic segments give the obstruction that denotes the limits of a cell.
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