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.
The DNA sequence of gene that change AACTTG to AACATG are called missense mutation. This is known as a process.
A frameshift mutation, such as an insertion of one nucleotide, is most likely to produce a protein with one extra amino acid. This type of mutation shifts the reading frame of the genetic code, leading to a change in the entire sequence of amino acids after the mutation site.
A mistake made during copying of genetic information is called a
A mutation
Sorry to burst the persons bubble that said frameshift mutation but its wrong. Point mutation-gene mutation involving changes in one or a few nucleotides. point mutation
it is a mutation like PLX4032 it reverses the effects of a mutation found in certain tumors
xx and xy genetic mutation.
a nonsense mutation
He doesn't have any mutations.
This depends on what kind of mutation occurs. You don't say what the mutation/result of the mutation is, so who knows what will happen to the monkey
tay-sachs disease
There are insertions and deletions (which both count as one kind) and substitutions (the second kind)
The sequence "tag ctt ggc" provided does not represent a specific mutation. A mutation would involve a change in a specific base or bases within a DNA sequence. Without further context or details, it is not possible to determine the type of mutation.
A frameshift mutation, such as an insertion of one nucleotide, is most likely to produce a protein with one extra amino acid. This type of mutation shifts the reading frame of the genetic code, leading to a change in the entire sequence of amino acids after the mutation site.
The DNA sequence of gene that change AACTTG to AACATG are called missense mutation. This is known as a process.
The mutation must be present in the Reproductive cell, Ovum/Egg in females (present in the Ovary) and Sperm in males.
a kind of mutation called deletion or insertion