The answer is; deletion mutation
This type of mutation mostly causes a phenomenon called frameshift mutation whereby the 3-codon sequence reading frame is shifted causing the amino acids translated, downstream of the deletion site, to be altered. This can gravely affect the function of the translated proteins and result in genetic disease.
Answer:
Hydrogen.
Explanation:
Hydrogen is the simplest chemical element that exists. The symbol for the chemical element Hydrogen is "H" and it is a colourless, tasteless, odorless, and highly flammable gas.
Hydrogen is a chemical element found in group (1) of the periodic table and as such it has one (1) electrons in its outermost shell. Therefore, Hydrogen has an atomic number of one (1) and a single valence electrons because it has only one proton and one electron in its nucleus.
Based on the octet rule which states that atoms of chemical elements gain, lose or share electrons so as to have eight (8) electrons in their valence shell. Therefore, atoms of chemical elements bond in order to attain the electronic configuration of a noble gas i.e a full valence shell which comprises of eight (8) electrons.
However, the chemical element "Hydrogen" is an exception to the octet rule because it is only able to hold a maximum of two (2) valence electrons in its outermost shell to become full.
<em>Hence, Hydrogen is an element which does not want to have eight valence electrons. </em>
Answer:
notochord, dorsal hollow nerve cord, pharyngeal slits, and a post-an4l tail
Explanation:
had to censor second to last word but the 4 is an a
It becomes more alkaline where pH will be more than 8
