0
The sequence was a result of a point mutation, which involves a change in a single nucleotide base. Frame shift mutations, on the other hand, involve insertions or deletions of nucleotides that shift the reading frame of a gene.
Add your answer:
Earn +20 pts
Can a point mutation be frameshift mutation?
No
Which of the following is a point mutation that does not produce a frame shift?
A point mutation that does not produce a frame shift is a synonymous mutation. This type of mutation occurs when a single nucleotide change in the DNA sequence does not change the amino acid that is encoded, as the genetic code is redundant.
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.
Name two major types of mutations?
Two major types of mutations are point mutations, which involve a change in a single nucleotide base in the DNA sequence, and chromosomal mutations, which involve changes in the structure or number of chromosomes.
Which type of mutation results in abnormal acid sequence?
A point mutation causes a change in the amino acid sequence creating a new type of protein. The mutations are categorized functionally as nonsense, missense and silent mutations.
Why is point mutation dangerous?
A frame shift mutation destroys the correct sequence of amino acids from the point of the mutation. The protein produced by a frame shift mutation would more than likely be nonfunctional.
Can a point mutation be frameshift mutation?
No
Which of the following is a point mutation that does not produce a frame shift?
A point mutation that does not produce a frame shift is a synonymous mutation. This type of mutation occurs when a single nucleotide change in the DNA sequence does not change the amino acid that is encoded, as the genetic code is redundant.
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.
How are point mutations and frame shift mutations different?
Point Mutations always result in [causing] a frame-shift mutation so they are the same.
What type of mutation is caused by adding one nucleotide into the middle of a sequence?
A frameshift mutation is caused by adding one nucleotide into the middle of a sequence. This type of mutation alters the reading frame of the genetic code, leading to a completely different amino acid sequence downstream of the insertion point.
Name two major types of mutations?
Two major types of mutations are point mutations, which involve a change in a single nucleotide base in the DNA sequence, and chromosomal mutations, which involve changes in the structure or number of chromosomes.
Can a frameshift mutation be a silnt mutation?
No, a frameshift mutation is not a silent mutation. Frameshift mutations result from the insertion or deletion of nucleotides in a DNA sequence, causing a shift in the reading frame during translation. This leads to a significant change in the amino acid sequence of the resulting protein, unlike silent mutations that do not change the amino acid sequence.
Would a point mutation or a frame shift mutation more likely produce a neutral mutation?
A point shift mutation is more likely to produce a neutral reaction. This is because it involves a change in one nucleotide. A frame shift mutation is more deleterious because it involves the insertion or deletion of multiple base pairs within a gene's coding sequence.
Which type of mutation results in abnormal acid sequence?
A point mutation causes a change in the amino acid sequence creating a new type of protein. The mutations are categorized functionally as nonsense, missense and silent mutations.
The substitution addition or removal of a single nucleotide in DNA is called a what mutation?
The substitution, addition, or removal of a single nucleotide in DNA is called a point mutation. This type of mutation can result in changes to the amino acid sequence of a protein, leading to potential functional consequences.
What type of mutation is a point mutation?
A point mutation is a type of mutation that involves a change in a single nucleotide in the DNA sequence. This can result in different types of mutations such as substitutions, insertions, or deletions of nucleotides.
