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If the mutation were in the gametes. Male and female reproductive cells.
yes but it would most likely be unnoticable
A mutation
The person's offspring will have mutated skin.
A frameshift mutation completely changes the genetic code from the point of the mutation, so the protein made as a result of the mutation would have the incorrect structure and would not function as it should.
A Base Substitution In Gametes During Meiosis
That species would have it's best chance of survival as a result of a mutation that has a high adaptive value that occurs in its gametes.
If the mutation were in the gametes. Male and female reproductive cells.
yes but it would most likely be unnoticable
A mutation
The person's offspring will have mutated skin.
Most likely result in mRNA that could not be translated and thus would not give rise to any proteins
A frameshift mutation completely changes the genetic code from the point of the mutation, so the protein made as a result of the mutation would have the incorrect structure and would not function as it should.
No. Skin cells are somatic cells. Your offspring come from gametes which are made by germ line cells. Only mutations in germ line cells or your gametes are passed on to your offspring.
A frame shift mutation destroys the correct sequence of amino acids from the point of the mutation. The protein produced by a frame shift mutation would more than likely be nonfunctional.
It would be worse in a gamete because it could be passed on to a child. Also, body cells usually eliminate a cell with a malfunction, but gametes do not.
Both types of mutation have the potential to cause a large effect.In general, a frameshift mutation is more likely to cause a large effect. This is because it shifts the 'reading frame' - so that all of the subsequent codons (groupings of 3 bases that are read to determine which amino acid will be added) will be changed.A point mutation is when a single base is replaced. This can either result in the same amino acid being added to the protein being synthesised (a silent mutation), a different amino acid being added (a missense mutation) or in a STOP codon (a nonsense mutation).If a point mutation causes a premature STOP codon - this is quite likely to have a large effect on the protein.