The answer is easy.
No
A frameshift mutation
A deletion mutation occurs when a nucleotide is dropped from a DNA sequence. This can cause a shift in the reading frame, leading to a non-functional protein being produced.
A frameshift mutation, where an insertion or deletion of nucleotides causes a shift in the reading frame of the genetic code, can change every amino acid that follows the point of mutation. This can have dramatic effects on the resulting protein's structure and function.
No
No
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.
A frameshift mutation
A deletion mutation occurs when a nucleotide is dropped from a DNA sequence. This can cause a shift in the reading frame, leading to a non-functional protein being produced.
A frameshift mutation is caused by the insertion or deletion of a nucleotide in the DNA sequence, leading to a change in the reading frame of codons. This can result in a completely different protein being produced from the altered sequence, affecting the functionality of the protein.
A frameshift mutation, where an insertion or deletion of nucleotides causes a shift in the reading frame of the genetic code, can change every amino acid that follows the point of mutation. This can have dramatic effects on the resulting protein's structure and function.
No
When the reading frame of a gene is altered, it can lead to a frameshift mutation where the sequence of codons is disrupted. This can result in a completely different protein being produced due to changes in the amino acid sequence. Frameshift mutations often lead to non-functional or dysfunctional proteins.
The addition or deletion of a nucleotide can lead to a Frameshift mutation. The Frameshift mutation causes a "shift" in the reading frame of the codons in the mRNA. This may lead to the change in the amino acid sequence at protein translation.
Insertion
frameshift mutation
A frameshift mutation is introduced by adding or deleting nucleotides in a DNA sequence that is not a multiple of three. This results in a shift in the reading frame during translation, leading to a completely different amino acid sequence downstream of the mutation. Frameshift mutations can have drastic effects on the resulting protein structure and function.