A point mutation that does not produce a frame shift is when one single base is replaced by a different base. This changes the DNA sequence, but does not cause a frame shift because it is a switch not an addition or subtraction of a base.
A point mutation is never a frameshift mutation because it involves the substitution of a single nucleotide for another rather than the insertion or deletion of nucleotides that would disrupt the reading frame of a gene.
Yes, a point mutation can result in a frameshift mutation if it occurs in a coding region of a gene and disrupts the reading frame of the genetic code.
No
No
A point mutation is not a frameshift mutation. Point mutations involve changes in a single nucleotide base, while frameshift mutations involve the insertion or deletion of nucleotide bases, causing a shift in the reading frame of the genetic code.
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.
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.
A point mutation is never a frameshift mutation because it involves the substitution of a single nucleotide for another rather than the insertion or deletion of nucleotides that would disrupt the reading frame of a gene.
Yes, a point mutation can result in a frameshift mutation if it occurs in a coding region of a gene and disrupts the reading frame of the genetic code.
Point Mutations always result in [causing] a frame-shift mutation so they are the same.
No
No
A point mutation is not a frameshift mutation. Point mutations involve changes in a single nucleotide base, while frameshift mutations involve the insertion or deletion of nucleotide bases, causing a shift in the reading frame of the genetic code.
Generally, a germ line mutation or sex cell mutation. Could be anything from a point mutation, one amino acid difference, to a whole frame shift mutation.
A 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.
Insertion mutations can affect many amino acids in the protein.An insertion mutation usually causes more defects during protein synthesis than point mutation because an insertion mutation will affect many amino acids in the protein.