answersLogoWhite

0

What else can I help you with?

Related Questions

During DNA replication an extra cytosine base is added to the DNA what type of mutation is this?

A frameshift mutation


What is insertion?

Insertion is a genetic mutation when an extra base is added to the DNA before or during replication


What two extra guanine bases are added to the DNA during DNA replication what mutation is this?

This is a frameshift mutation and will render the rest of the DNA sequence useless.


During DNA replication two extra guanine bases are added to the DNA. What type of mutation is this?

frameshift mutation


During the transcription of a certain protein an extra cytosine was placed into a gene region throwing off the correct amino acid sequence what type of mutation occurred?

This is an example of an insertion mutation, where an extra nucleotide (cytosine in this case) is added to the DNA sequence during transcription, causing a shift in the reading frame and resulting in a change in the amino acid sequence of the protein being produced.


To what end are nucleotides added during DNA replication?

Nucleotides are added during DNA replication to create a new complementary strand of DNA, ensuring accurate genetic information is passed on to daughter cells during cell division.


Mutation results from an extra nucleotide being added into the sequence?

Not necessarily. Mutations can result from a variety of changes to the DNA sequence, including substitutions, deletions, or insertions of nucleotides. These changes can be spontaneous errors during DNA replication, exposure to mutagens, or environmental factors.


Which type of mutation results when bases are added to a gene?

An insertion mutation occurs when extra bases are added into a gene. This can disrupt the reading frame, leading to a shift in the way the genetic code is interpreted during protein synthesis.


What causes DNA variation in organisms?

Mutation of the genetic code causes DNA variation in organisms. For example, during DNA replication, one nitrogen base may be substituted for another, or an extra base can be added, or a nitrogen base can be skipped. If any of these mutations occur during the formation of gametes (sex cells), then the offspring that receives the mutation may have a genetic disorder.


A mutation in which a single base is added to or deleted from DNA is called what?

A mutation in which a single base is added to or deleted from DNA is called an insertion or deletion mutation, also known as an indel mutation. This can lead to a shift in the reading frame during translation, causing significant changes in the resulting protein sequence and potentially leading to functional consequences.


What is a nucleotide substitution error?

Before you know what a nucleotide substitution error is, you have to know what a nucleotide is. A nucleotide holds the DNA strand together and helps make copies. When a Strand is ready to be copied, Let's say one nucleotide reads for G(Guanine), then another nucleotide would be added, which would mean C (Cytosine) would be added. A substitution error would mean that, that instead of Cytosine being added, Thymine, Adenine, Uracil, or Guanine could be added, resulting in a mutation.


When a extra base is added to an organism DNA the mutation is known as a?

frameshift mutation.