Answer:
(A). Result in different amino acids to be read due to frame shifts
Explanation:
Insertion or deletion mutations (or Indel mutations) can be defined as mutations in DNA due to insertion (addition) or deletion of nucleotide bases in DNA.
These mutations lead to change in reading frames (sequence of codons), which leads to formation of protein having completely different amino acid sequence. Hence, these mutations are also cause frameshift mutations.
This is due due to triplet nature of genetic codes as insertion or deletion of one or more bases (but not three) would change change in codon sequence and mutated sequence can form a non-functional or truncated protein.
Thus, the correct answer is option (A).
Answer:
Both
Explanation:
Well,it has both good and bad aspects.In my opinion,hereditary traits possess good side through the genetic factors whereas it shows negativity as it may cause some diseases or hard complications.
If it doesnt have a nucleus or a cell wall it is a prokaryote. also prokaryotes displayed in pictures tends to be longer
An irregularly occurring and complex series of climatic changes affecting the equatorial pacific region and beyond every few years, characterized by the appearance of unusually warm, nutrient-poor water off northern Peru and Ecuador, typically in late December
Answer:
Yes.
Explanation:
The energy released in splitting just one atom is miniscule. However, when the nucleus is split under the right conditions, some stray neutrons are also released and these can then go on to split more atoms, releasing more energy and more neutrons, causing a chain reaction.