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28 Sep 2019
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 geneâs intron? Why?
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 geneâs intron? Why?
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Nestor RutherfordLv2
28 Sep 2019