If one or more nucleotide pairs are deleted from a DNA strand, this is known as a frameshift mutation
<h3>
Define Frameshift Mutation</h3>
Insertions or deletions in the genome that are not multiples of three nucleotides are referred to as frameshift mutations. They are a particular class of insertion-deletion (indel) alterations that are present in polypeptides' coding sequences. Here, there are no multiples of three in the number of nucleotides that are added to or subtracted from the coding sequence. They may result from really basic alterations like the insertion or deletion of a single nucleotide.
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Frameshift mutations' effects</h3>
One of the most harmful modifications to a protein's coding sequence is a frameshift mutation. They are quite prone to produce non-functional proteins that frequently interfere with a cell's metabolic processes and result in significant alterations to polypeptide length and chemical makeup. Frameshift mutations can cause the mRNA to stop translating too soon and create an extended polypeptide.
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Answer:
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<em>m = </em><u><em>25</em></u><em> </em><em> </em><u><em>Kg</em></u>
Answer:
Three hydrogen atoms to form PH₃.
Explanation:
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In this case, since the elements belonging to the nitrogen family (N, P, As, Sb and Bi) show five valence electrons, because there are five electrons at their outer shell, it is clear that if phosphorous bonds with hydrogen, it is going to require the same amount of oxygen atoms (3) because elements having five valence electrons need 3 bonds in order to attain the octet (5+3=8).
Therefore the compound would be:
Which is phosphine.
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