Answer:
A mutation in the DNA sequence of the gene for brown fur
Explanation:
The mutations are capable of changing the encoded protein product, in this case the gene that encodes for the fur color pigment. This mutation may have occurred during mitosis or meiosis divisions.
If it is a spontaneous mutation that occurred in the germinal line (meiosis) and confers an adaptive advantage, it will increase their frequency in the population.
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X-linked disorder is a recessive autosomal disorder, which means that
There is a 1 in 4 chance (25%) of having a child who is unaffected.
There is a 1 in 4 chance (25%) of having a child who is affected by the condition. These children have two copies of the gene that do not work correctly.
There is a 1 in 2 chance (50%) of having a child who is a carrier of the condition. These children have one working copy of the gene and one copy of the gene that does not work correctly.
I'd say A: tidal waves. B, C, and D don't really seem to fit for me.
