Base-Pair insertions or deletions
a frameshift mutation
Deletion
Insertion
Point Mutation- a type of gene mutation in which only a single nucleotide in a gene has been changed.
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 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 frameshift mutation will have the most serious effects.A frameshift mutation is a type of mutation involving the insertion or deletion of a nucleotide in which the number of deleted base pairs is not divisible by three.Divisible by three is important because the cell reads a gene in groups of three bases.Each group of three bases corresponds to one of 20 different amino acids used to build a protein.If a mutation disrupts this reading frame, then the entire DNA sequence following the mutation will be read incorrectly.
deletion
deletion
frameshift mutation
Insertion?
Insertion
Point Mutation is the mutation that involves a single or few nucleotide. This type of mutation replaces a single nucleotide to another.
deletion mutation
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.
Point Mutation- a type of gene mutation in which only a single nucleotide in a gene has been changed.
A point mutation is a type of genetic mutation that involves a change in a single nucleotide base pair in DNA. This can result in the substitution of one nucleotide for another, the insertion of an extra nucleotide, or the deletion of a nucleotide. Point mutations can lead to changes in the amino acid sequence of a protein, which can affect its structure and function.
A frame-shift mutation.
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