Many different types of mutations can occur within the body. Sickle cell anemia is a disease that occurs when a mutation in the base pair of the hemoglobin beta gene causes a single replacement of the amino acid glutamic acid by the amino acid valin. As a result of this mutation the individual’s blood cells take on a sickle shape under certain conditions Which type of mutation causes sickle cell anemia

POINT MUTATION (SUBSTITUTION)

Explanation:

A point mutation is that mutation which involves only one nucleotide base. Point mutation can, however, occur in different ways such as SUBSTITUTION. Substitution point mutation is that which involves the replacement of a single nucleotide base by another in a gene sequence.

This is the case in this question regarding the mutation that causes sickle cell anaemia. According to this question, Sickle cell anemia is a disease that occurs when a mutation in the base pair of the hemoglobin beta gene causes a SINGLE replacement of GLUTAMIC ACID (Glu) by VALINE (Val). This shows that it is a type of SUBSTITUTION POINT MUTATION.

carbohydrates: (starches and sugars) composed of carbon, hydrogen, and oxygen.

lipids: (fats, oils, and waxes) are made of carbon and hydrogen atoms.

nucleic acids: contain hydrogen, oxygen, nitrogen, carbon, and phosphorus. they are polymers of nucleotides. a nucleotide has three parts, a 5-carbon sugar, a phosphate     (-po⬇️4) group, and a nitrogenous base.

proteins: made up of nitrogen, carbon, hydrogen, and oxygen. they are polymers of amino acids.