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When a nitrogen base is substituted for a different one so it may code for a different amino acid. Sometimes substitution still codes for a same amino acid, in which case it becomes a silent mutation, but in other times it may alter the protein entirely.
What else can I help you with?
Which is not a frameshift mutation substitution insertion deletion or point mutation?
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.
What is never a frameshift mutation?
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.
What type of mutation occurred in the strand of DNA?
A point mutation occurred in the DNA strand. This is a change in a single nucleotide base, such as a substitution, insertion, or deletion.
Which type of mutation occurs when one base replaces another base in a DNA condon?
A point mutation occurs when one base replaces another base in a DNA codon. This type of mutation can result in a different amino acid being incorporated into the protein sequence, which may affect the structure and function of the protein. Examples of point mutations include substitutions, insertions, and deletions of a single base pair.
Mutations that change one or just a few of nucleotides in a gene on a chromosome are called what?
the correct answer is C. a substitution i know this cause i have this book to this question and point mutation is not one of the answer and i found the answer in the book -No its substituton you jack wagon your books wrong
A change in a single nucleotide in DNA-?
A mutation
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.
Which is not a frameshift mutation substitution insertion deletion or point mutation?
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.
What are two types of mutation?
From another angle: beneficial and detrimental.
What is never a frameshift mutation?
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.
If one nucleotide is replaced by another it is called?
If one nucleotide is replaced by another, it is called a point mutation. This type of mutation involves a change in a single nucleotide within the DNA sequence.
What type of mutation occurred in the strand of DNA?
A point mutation occurred in the DNA strand. This is a change in a single nucleotide base, such as a substitution, insertion, or deletion.
Which type of mutation occurs when one base replaces another base in a DNA condon?
A point mutation occurs when one base replaces another base in a DNA codon. This type of mutation can result in a different amino acid being incorporated into the protein sequence, which may affect the structure and function of the protein. Examples of point mutations include substitutions, insertions, and deletions of a single base pair.
Mutations that change one or just a few of nucleotides in a gene on a chromosome are called what?
the correct answer is C. a substitution i know this cause i have this book to this question and point mutation is not one of the answer and i found the answer in the book -No its substituton you jack wagon your books wrong
The DNA sequence of a gene changed from AACTTG to AACATG. What kind of mutation occurred.?
The DNA sequence of gene that change AACTTG to AACATG are called missense mutation. This is known as a process.
What is one example of a substitution mutation?
One common example of a substitution mutation is a point mutation where one nucleotide base is replaced by another. This can lead to changes in the amino acid sequence of a protein during translation. An example would be a mutation where a Cytosine (C) is substituted for a Thymine (T) in the DNA sequence.
What is a mutation you might have but not know about?
substitution
