a silent mutation.
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.
Point mutation and it can be effective or silent depend upon at the site of codon
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.
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.
a silent mutation.
AGG-Apex
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.
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.
Point mutation and it can be effective or silent depend upon at the site of codon
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.
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.
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.
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.
When a mutation does not change the result of a normal production of a protein is called harmless. This is because it does no harm to the individual.
a mutation that does not affect protein production.
A mutation that alters the base but not the amino acid is called a "silent mutation." This type of mutation occurs when a change in the DNA sequence does not affect the protein's primary structure due to the redundancy in the genetic code, where multiple codons can code for the same amino acid. Consequently, the resulting protein remains unchanged despite the alteration in the nucleotide sequence.