Question

In sickle cell anemia . Describe what is single base substitution?

Answer 1

Answer:

Explanation:

Genetics of Sickle Cell Anemia

The mutation causing sickle cell anemia is a single nucleotide substitution (A to T) in the codon for amino acid 6. The change converts a glutamic acid codon (GAG) to a valine codon (GTG). The form of hemoglobin in persons with sickle cell anemia is referred to as HbS

Answer 2

Answer:

HEY MATE HERE IS YOUR ANSWER...

Genetics of Sickle Cell Anemia

The mutation causing sickle cell anemia is a single nucleotide substitution (A to T) in the codon for amino acid 6. The change converts a glutamic acid codon (GAG) to a valine codon (GTG). The form of hemoglobin in persons with sickle cell anemia is referred to as HbS

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