Well consider the substitution of one hydrophillic amino acid for another hydrophillic amino acid. This type of mutation changes nothing but a molecular marker.
or
Silent
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.
A mutation can change a codon for one amino acid into a different codon for the same amino acid through a process called silent mutation. This type of mutation occurs when a change in the DNA sequence does not alter the amino acid that is coded for, resulting in the same protein being produced.
Well consider the substitution of one hydrophillic amino acid for another hydrophillic amino acid. This type of mutation changes nothing but a molecular marker. or Silent
A point mutation, specifically a missense mutation, is responsible for the formation of a protein with one incorrect amino acid. This type of mutation involves a single nucleotide change in the DNA sequence, leading to the substitution of one amino acid in the protein.
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 silent mutation
A mutation that causes the code for the wrong amino acid (apexvs.com)
A silent mutation is an example of a mutation that would not affect an organism's phenotype. This type of mutation occurs in a non-coding region of DNA, such as an intron, and does not change the amino acid sequence of the protein produced. Therefore, it has no impact on the organism's outward appearance or characteristics.
Missense
Yes, it already has by changing the amino acid you have a mutation. That one amino acid counld be in the active site of an enzyme and that one amino acid being changed could result in loss of function or reduction in function of the enzyme. Sickle cell animea is caused by a single such amino acid substiution.
A substitution mutation is a type of genetic mutation where one nucleotide is replaced by another in the DNA sequence. This can lead to a change in the amino acid sequence during protein synthesis, which can alter the function of the protein produced. The impact of a substitution mutation on the genetic code depends on where it occurs in the DNA sequence and what amino acid is substituted, which can result in a variety of effects ranging from no change to a significant alteration in the protein's function.
A point mutation is a change in a single nucleotide in the genetic code, while a non-synonymous mutation is a type of point mutation that causes an amino acid change in the resulting protein. Non-synonymous mutations can affect the function of the protein, while synonymous mutations do not change the amino acid sequence.