Answer:
A mutation is the changing of the structure of a gene, resulting in a variant form that may be transmitted to subsequent generations, caused by the alteration of single base units in DNA, or the deletion, insertion, or rearrangement of larger sections of genes or chromosomes. Mutations in sex cells are more serious because they are heritable and affect the next generation.
Explanation:
Absorption takes place in the small intestine. Fatty acids and glycerol are formed by digestion of lipids which diffuse through the one-cell thick cell wall of villi and into lacteals (lymphatic vessels).
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