I believe it is B i took this test last year.
Based on the above information, the mutation type is frameshift mutation.
It is a genetic mutation caused by indels of various nucleotides in a DNA succession that is not detachable by three. The additions and erasures cause an adjustment in the length of a quality, which causes a movement in the codon perusing outline. A frameshift mutation happens when a protein is radically modified as a result of an addition or an erasure. Tay-Sachs illness is a human issue caused by a frameshift change.
Answer:
answer a is trash answer b add a vertical line
Explanation:
Its the person's offspring have mutated skin.
because for a mutation to be passed down to an offspring mutation has to happen in the sex cells. so that is the least likely to happen.
since the other may happen for example.
skin cancer: i am not sure how but definitely sure that it is the second least that is gonna happen. (trust me)
reduced functioning of skin cell yes.: if there are changes in the nucleotides which can give a diff amino acid.
and no change. cuz if the mutation occurs but the nucleotides still codes for the same amino acid then there is no problem!!
I would say the microscope....................
