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What change to this sequence would indicate a silent mutation?
A silent mutation occurs when a change in the DNA sequence does not alter the amino acid sequence of the resulting protein. This can happen through a substitution of a nucleotide that still codes for the same amino acid due to the redundancy of the genetic code. For example, if the original sequence is "GAA" (which codes for glutamic acid) and it changes to "GAG," this would represent a silent mutation since both codons code for the same amino acid. Thus, the change in the sequence that doesn't affect the protein's amino acid sequence indicates a silent mutation.
What is a A genetic mutation that does not result in a change in the amino acid sequence of the resulting protein is called?
a silent mutation.
What type of mutation is likely to have the least effect on an organism?
A silent mutation, where a change in the DNA sequence does not result in a change to the amino acid sequence of the protein, is likely to have the least effect on an organism. This is because the protein produced is unaffected, and therefore the organism's functioning remains unchanged.
A mutation that occurs at a specific location within a nucleotide sequence is called a?
Point mutation and it can be effective or silent depend upon at the site of codon
What codes for the same silent point mutation?
A silent point mutation is a change in a DNA sequence that does not alter the amino acid sequence of the resulting protein. This often occurs due to the redundancy of the genetic code, where multiple codons can code for the same amino acid. For instance, both GAA and GAG codons code for glutamic acid, so a mutation from GAA to GAG would be a silent mutation. Thus, any codon that codes for the same amino acid as the original codon can be considered as coding for the same silent point mutation.
What change to this sequence would indicate a silent mutation?
A silent mutation occurs when a change in the DNA sequence does not alter the amino acid sequence of the resulting protein. This can happen through a substitution of a nucleotide that still codes for the same amino acid due to the redundancy of the genetic code. For example, if the original sequence is "GAA" (which codes for glutamic acid) and it changes to "GAG," this would represent a silent mutation since both codons code for the same amino acid. Thus, the change in the sequence that doesn't affect the protein's amino acid sequence indicates a silent mutation.
What is a A genetic mutation that does not result in a change in the amino acid sequence of the resulting protein is called?
a silent mutation.
A part of an mRNA has the sequence CAU Use the table below to figure out which amino acid is coded for by CAU then use the table to figure out which change to this sequence would indicate a silent?
AGG-Apex
Which mutation would not change the remainder of the reading frame of a gene sequence that follows the mutation?
A silent mutation, where a nucleotide substitution results in a codon that codes for the same amino acid, would not change the remainder of the reading frame of a gene sequence. This is because the amino acid sequence produced by the altered codon remains the same.
What type of mutation is likely to have the least effect on an organism?
A silent mutation, where a change in the DNA sequence does not result in a change to the amino acid sequence of the protein, is likely to have the least effect on an organism. This is because the protein produced is unaffected, and therefore the organism's functioning remains unchanged.
A mutation that occurs at a specific location within a nucleotide sequence is called a?
Point mutation and it can be effective or silent depend upon at the site of codon
What codes for the same silent point mutation?
A silent point mutation is a change in a DNA sequence that does not alter the amino acid sequence of the resulting protein. This often occurs due to the redundancy of the genetic code, where multiple codons can code for the same amino acid. For instance, both GAA and GAG codons code for glutamic acid, so a mutation from GAA to GAG would be a silent mutation. Thus, any codon that codes for the same amino acid as the original codon can be considered as coding for the same silent point mutation.
What is a silent muation?
A silent mutation is a type of genetic mutation that does not result in any change to the amino acid sequence of a protein due to redundancy in the genetic code. These mutations often occur in the third position of a codon and are therefore considered "silent" because they do not affect the resulting protein.
If a strand of DNA with the sequence TGA mutated to GCA would it be a silent or missense mutation?
Both a silent and missense mutation is a change in one nucleotide. However, a silent mutation still codes for the same amino acid, but a missense mutation codes for a different amino acid. This means that a silent mutation will have no affect on the resulting protein, but a missense mutation will. Still, it is not guaranteed that a a missense mutation will result in a disfunction of created protein, as long as it is not occurring in the activation site.
What type of mutation does not change the change the amino acids produced?
A silent mutation is a type of mutation that does not change the amino acids produced. This occurs when a change in the DNA sequence does not alter the corresponding codon, often due to the redundancy of the genetic code. As a result, the protein remains unchanged, maintaining its normal function.
What is a mutation called that has no effect on an organism?
A point mutation, in which one nitrogen base in a codon is substituted for another, may have no effect on an organism. This is true if the base substitution does not change the amino acid that the codon represents, or if the mutation occurs in a non-critical location in the protein so that the protein's structure is not changed significantly and the protein is still able to function.
Can a frameshift mutation be a silnt mutation?
A frameshift mutation completely changes the genetic code from the point of the mutation, so the protein made as a result of the mutation would have the incorrect structure and would not function as it should.
