When a single nucleotide base pair is substituted, type of mutation occurs is?
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A substitution is a mutation that exchanges one base for another (i.e., a change in a single "chemical letter" such as switching an A to a G). Such a substitution could: change a codon to one that encodes a different amino acid and cause a small change in the protein produced.
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This type of mutation is called point mutation , but if nucleotide added or deleted then it’s called the frame shift mutation , example of the point shift mutation is sickle cell anaemia
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