Answer: The mutation is substitution.
Explanation:
There are three main types of mutation:
Substitution, deletion, and insertion.
We would be able to tell right away if the second sequence had an insertion or deletion, because it would have a different number of letters than first sequence. However, it does not. Both sequences have 12 letters.
But, the 8th letter in the first sequence (T) is different from the 8th letter in the second sequence (A).
This is substitution.
Answer:
Codominant- traits don’t have a clear dominant or recessive
incomplete dominance- the heterozygous condition shows a “blending” or a “middle” condition
Explanation:
In codominance, the traits are expressed equally in the phenotype thus they don't have a clear dominant or recessive state. For example the ABO blood group alleles. The alleles A and B are codominant each being expressed equally.
In incomplete dominance the traits show intermediate expression where one allele expresses itself more strongly than the other. An example in man is seen in the inheritance of the disease sickle cell anaemia. Heterozygote who carry the sickle cell gene are said to have sickle cell trait and as such the carrier allele (HBa) has a stronger influence on the phenotype than the dominant alle (HBs).
The thing that makes kes73 interesting to astronomers is ; ( A ) A second star.
kes73 is believed by astronomers to have come from the explosion of dying stars in the supernova. The gases from the dying stars explode and scatter across forming a colorful cloud known as kes73.
At the center of the colorful cloud formed from the gases of the dying stars is a second star ( magnetar ) which is the most powerful star in the galaxy due to its magnetic force.
Hence we can conclude that the thing that makes kes73 interesting to astronomers is the presence of a second star
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<span>a large body of water surrounded by land.</span>
