A frameshift mutation is a genetic mutation due to insertions or deletions of a number of nucleotides in a DNA sequence which is not divisible by three. Due to the triplet nature of gene expression by codons, the insertion or deletion can change the grouping of the codons, resulting in a completely different translation from the original.
Question : Thalassemia is an example of
Option 1: Deletion mutation
Option 2: Point mutation
Option 3: Silent mutation
Option 4: Frame shift mutation
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