Biology, 17.04.2020 19:04 SassyBanana
Which of the following mutations would most likely be identified as a chromosomal translocation?
A sequence of bases encodes for genes XXY. A portion of another chromosome breaks off and inserts within genes XYZ.
A mutation occurs while copying a chromosome. Instead of reading EFGHI, the chromosome reads EFGFGHI.
The genetic sequence is MNOPQ. A mutation occurs and the sequence of bases that encodes for gene N is not copied.
The sequence of bases on the mRNA reads CUU and codes for the amino acid Leucine. A mutation occurs and the mRNA sequence changes to CCU and now codes for the amino acid Proline.
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Which of the following mutations would most likely be identified as a chromosomal translocation?
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