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What is more likely to have a detrimental effect on the phenotype: a 3 base pair deletion from the middle of the coding sequence of a gene, or a 8 base pair deletion from the same region of the gene? Why? Would the outcome be different if the deletions happened within the gene’s intron? Why?

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Nestor Rutherford
Nestor RutherfordLv2
28 Sep 2019

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