Explanation:
Yes they can. An AB parent can indeed sometimes have an O child. But it is by no means common. In fact it would be fair to say that it is exceedingly rare.
The one exception is in certain Asian groups. Some of these folks have a rare version of the ABO blood type gene called cis-AB. People with this gene version have an AB blood type but can easily have an O child.
Answer:
A convergent plate boundary is a location where two tectonic plates are moving toward each other, often causing one plate to slide below the other (in a process known as subduction). The collision of tectonic plates can result in earthquakes, volcanoes, the formation of mountains, and other geological events.
Explanation:
The location where two plates meet is called a plate boundary. Plate boundaries are commonly associated with geological events such as earthquakes and the creation of topographic features such as mountains, volcanoes, mid-ocean ridges, and oceanic trenches.
Answer:
Indian
Explanation:
hi stay safe stay healthy
There are many ways humans can reduce the amount of endangered and extinct species. However, I would say by reducing pollution and logging/mining. Nearly 318 species have become extinct due to pollution. The reduction of carbon emissions would be a good way to curb the amount of pollution produced by humans.
Answer:
mRNA: 3' AUG-AAU-GCU-GCC-GGU-GA-5'
amino acids : methionine, asparagine, alanine, arginine, proline
type of mutation: deletion, missense
Explanation:
The mRNA sequence is complementary to the DNA sequence. A always pairs with T, C always pairs with G. Except this is an RNA sequence not a DNA sequence, so T is replaced with U.
The mRNA sequence is translated into an amino acid sequence based on the triplet code. The triplet code for this sequence is shown in the attached picture. Each triplet signifies a specific amino acid. The codon can be identified from the table and placed in sequence. We can see that the new DNA strand has caused a new amino acid sequence. It has also left us with an incomplete sequence, as GA cannot signify an amino acid.
The type of mutation is a single base deletion. We can see that the base C is missing from the 9th amino acid in the original strand. As you can see, this has an ongoing affect on all the bases in the rest of the sequence, as it changes the way the sequence is organised into codons. This results in a missense mutation.