THE MOLECULAR BASIS OF INHERITANCE
GENE MUTATION
Question
[CLICK ON ANY CHOICE TO KNOW THE RIGHT ANSWER]
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Substitution
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Deletion
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Insertion
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Frameshift
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Detailed explanation-1: -Such a substitution could: change a codon to one that encodes a different amino acid and cause a small change in the protein produced. For example, sickle cell anemia is caused by a substitution in the beta-hemoglobin gene, which alters a single amino acid in the protein produced.
Detailed explanation-2: -Other common mutation examples in humans are Angelman syndrome, Canavan disease, color blindness, cri-du-chat syndrome, cystic fibrosis, Down syndrome, Duchenne muscular dystrophy, haemochromatosis, haemophilia, Klinefelter syndrome, phenylketonuria, Prader–Willi syndrome, Tay–Sachs disease, and Turner syndrome.
Detailed explanation-3: -Substitution mutations can be good, bad, or have no effect. They cause three specific types of point mutation: silent, missense, and nonsense mutations. A silent mutation is one where the function of the protein is not changed. A missense mutation codes for the wrong protein.