there are three kind of mutation exist: insertion, deletion, substitution
In figure 11-4, a frameshift mutation has occurred. This type of mutation involves the insertion or deletion of nucleotides that shifts the reading frame of the genetic code, leading to changes in the amino acid sequence of the resulting protein.
A chromosomal mutation can occur either during the formation of the egg or sperm, or after fertilization when the zygote is forming. This means the mutation could have occurred in the parent's gametes, or during cell division in the early stages of embryo development.
The specific type of mutation resulting from a mistake during DNA replication will depend on the nature of the mistake and the type of nucleotide substitution that occurred. Some possible types of mutations include point mutations (such as a substitution, insertion, or deletion of a single nucleotide), frameshift mutations, or silent mutations.
during meiosis
Selective reverse mutation refers to a process in which a specific mutation that had previously occurred in an organism is corrected or reverted back to the original DNA sequence. This can happen naturally or can be induced by various genetic or environmental factors.
The DNA sequence of gene that change AACTTG to AACATG are called missense mutation. This is known as a process.
A point mutation occurred in the DNA strand. This is a change in a single nucleotide base, such as a substitution, insertion, or deletion.
a point mutation
A mutation in a sex cell means that the mutation can be passed on to the individuals offspring. If the mutation just occurred in a somatic cell, it would not be passed down.
46 unless a mutation has occurred
In figure 11-4, a frameshift mutation has occurred. This type of mutation involves the insertion or deletion of nucleotides that shifts the reading frame of the genetic code, leading to changes in the amino acid sequence of the resulting protein.
A chromosomal mutation can occur either during the formation of the egg or sperm, or after fertilization when the zygote is forming. This means the mutation could have occurred in the parent's gametes, or during cell division in the early stages of embryo development.
it is a mutation like PLX4032 it reverses the effects of a mutation found in certain tumors
xx and xy genetic mutation.
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.
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.
a nonsense mutation