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What cause substitution mutation

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The answer for this question is sickle cell anemia

User Muhammed Albarmavi
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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. ... These are called silent mutations.

User Josh From Qaribou
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