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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 else can I help you with?
As a result of the incorrect sequence of amino acids will be translated into a protein-resulting in a mutation?
Missence mutation
Which type of point mutation would be insignificant to the organism?
A silent mutation is typically insignificant to the organism. This type of point mutation occurs when a change in the DNA sequence does not alter the amino acid sequence of the resulting protein, often due to the redundancy in the genetic code. As a result, the protein's function remains unchanged, and the organism is usually unaffected by this mutation.
Most genetic disorders results from a mutation that changes the amino acid sequence in a?
Most genetic disorders result from a mutation that changes the amino acid sequence in a protein. This change can lead to altered protein function, which can affect normal cellular processes and result in disease.
What type of mutation alters the base but not the amino acid?
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.
What type of mutation has occurred in figure 11-4?
In figure 11-4, a frameshift mutation has occurred. This type of mutation involves the insertion or deletion of nucleotides that shifts the reading frame of the genetic code, leading to changes in the amino acid sequence of the resulting protein.
As a result of the incorrect sequence of amino acids will be translated into a protein-resulting in a mutation?
Missence 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.
What is a substitution mutation and how does it impact the genetic code?
A substitution mutation is a type of genetic mutation where one nucleotide in the DNA sequence is replaced with a different nucleotide. This can lead to changes in the amino acid sequence during protein synthesis, potentially altering the function of the protein. The impact of a substitution mutation on the genetic code depends on where it occurs and what specific nucleotide is substituted.
Most genetic disorders results from a mutation that changes the amino acid sequence in a?
Most genetic disorders result from a mutation that changes the amino acid sequence in a protein. This change can lead to altered protein function, which can affect normal cellular processes and result in disease.
What chemical found in a gene is changed by mutation?
The chemical found in a gene that is changed by mutation is the sequence of nucleotides comprising the genetic code. Mutations can alter this sequence by substituting, inserting, or deleting nucleotides, which can lead to changes in the resulting protein or RNA molecule.
What describes a substitution mutation and how does it impact the genetic code?
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.
What type of mutation alters the base but not the amino acid?
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.
What is the impact of a frameshift mutation, where one or more pairs of nucleotides are removed from a gene, on the resulting protein product?
A frameshift mutation, where nucleotides are removed from a gene, can change the reading frame of the gene. This alters the sequence of amino acids in the resulting protein, leading to a non-functional or abnormal protein. This can have serious consequences on the protein's structure and function, potentially causing genetic disorders or diseases.
What type of mutation has occurred in figure 11-4?
In figure 11-4, a frameshift mutation has occurred. This type of mutation involves the insertion or deletion of nucleotides that shifts the reading frame of the genetic code, leading to changes in the amino acid sequence of the resulting protein.
What is substitution mutation and how does it impact genetic variation in biology?
A substitution mutation is a type of genetic mutation where one nucleotide in the DNA sequence is replaced with a different nucleotide. This can lead to changes in the amino acid sequence during protein synthesis, potentially altering the function of the protein. Substitution mutations can impact genetic variation by introducing new genetic variations within a population, which can contribute to evolution and diversity.
What is a genetic mutation that does not result in a change in the amino acid sequence of the resulting protein?
It is neutral mutation. Codons are made up of 3 base pairs. This gives 64 different combinations, but there are only 20 amino acids, so some different codons will code for the same amino acid. When the base pair that is changed doesn't cause a change in the amino acid it codes for, then ultimately nothing happens
What is the difference between point and non-synonymous mutation?
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.
