The sequence TGA-GCC-ATG-A is changed in 2 places to become TGA-GCA-CAT-GA.
When one base is changed, it is called a point mutation.
In this case, a GCC in the DNA has been changed to a GCA. This would mean the mRNA codon (coded for by this DNA) would change from CGG to CGU.
Both of these codons code for the same amino acid - Arginine. Therefore this type of point mutation is known as a silent mutation.
The extra C that appears would be called an addition mutation, which is a type of frameshift mutation.
If the DNA sequence tgagccatga is changed to tgagcacatga, a deletion mutation has occurred.
The DNA sequence of gene that change AACTTG to AACATG are called missense mutation. This is known as a process.
No that occurs all the time through translocation. It is not a mutation.
Any change in the sequence of DNA nucleotides is called mutation.
A mutation is a change from the expected nucleotide sequence of DNA. It can happen when nucleotide bases are duplicated or deleted from the sequence.
A mutation in a DNA nucleotide sequence would be more harmful than a mutation in a mRNA nucleotide sequence because it could cause the synthesis of multiple nonfunctional proteins in comparison to a mutation in a mRNA nucleotide sequence that would be less harmful because it would result in a few nonfunctional proteins.
The DNA sequence of gene that change AACTTG to AACATG are called missense mutation. This is known as a process.
The comparison between the DNA sequence of normal DNA to the mutated DNA will be made. The type of mutation will be revealed during the base sequence.
No that occurs all the time through translocation. It is not a mutation.
Any change in the sequence of DNA nucleotides is called mutation.
A Displacement Mutation has occured.
A mutation is a permenent in DNA sequence of a gene,mutation in a gene's DNA sequence can alterthe aminoacid sequence of the protein encodedby the gene.
a change in the DNA sequence is a mutation, so I'm not sure what you're asking
A mutation is a change from the expected nucleotide sequence of DNA. It can happen when nucleotide bases are duplicated or deleted from the sequence.
Missence mutation
A mutation in a DNA nucleotide sequence would be more harmful than a mutation in a mRNA nucleotide sequence because it could cause the synthesis of multiple nonfunctional proteins in comparison to a mutation in a mRNA nucleotide sequence that would be less harmful because it would result in a few nonfunctional proteins.
The answer is easy.
frameshift mutation