Answer:
your answer it is help to understand this question
Answer: There will be no effect on the protein produced
Explanation:
According to the genetic code, the triplet codon GAG code for the amino acid, glutamate, while GAC code for aspartate.
Since GAG and GAC code for amino acids with similar properties (aspartate and glutamate are both acidic amino acids due to the extra carboxyl group present in their side chain), the change in nucleotide is still similar to the original, so will result in a different amino acid sequence, but will not alter the function of the protein at all. Thus, this kind of mutation is called silent mutation.
The answer is B
Before the process of translation occurs, mRNA which bears the blue print or coded information for the synthesis of a specific protein arrives from the nucleus and into the cytoplasm where there are ribosomes
mRNA then attaches itself to a ribosome. The ribosome is the site where the protein is formed. It is sometimes referred to as the "work bench" of the cell. Once mRNA is attached, tRNA comes and begins to read and translate the coded information on the mRNA. This is the translation stage of protein synthesis.
Based on the translated information, tRNA then fetches amino acids from the pool of free amino acids found in the cytoplasm and brings them to the ribosome where they are joined to form a chain thus creating a protein.
Definition-change in a population or species over time.
This would be probably true if the assumption that all possible genotypic variations would be equally distributed (so we would have 25% HH, 25% hh and 2x 25 Hh). If this distribution would be true and Huntingtons disease really was a single gene dominant trait diesase, then yes, we could expect such a distribution in the population.
