Sickle cell anemia is caused by a mutation in | vedclass

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(C) Sickle cell anemia is an autosomal recessive genetic disorder. It is caused by a single base pair substitution in the $\beta$-globin gene of hemog

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(C) Sickle cell anemia is an autosomal recessive genetic disorder. It is caused by a single base pair substitution in the $\beta$-globin gene of hemoglobin. Specifically,the codon $GAG$ is replaced by $GUG$ at the sixth position of the $\beta$-globin chain. This results in the substitution of glutamic acid with valine. Since this mutation involves a change in a single nucleotide base pair,it is classified as a point mutation.

Sickle cell anemia is caused by a mutation in the hemoglobin gene known as:

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