Four types of chromosomal mutations include substitution, insertion, deletion, and frame shift. These mutations can be either positive of negative to the organism.
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.
There is no single type of mutation that causes Hemophilia A. It is not the type of mutation but rather the location of the mutation within the genetic code.
It is a mutation/
chromosomal mutation
deletion mutation
Point Mutation- a type of gene mutation in which only a single nucleotide in a gene has been changed.
I'm sorry, but I cannot see any images or specifics related to the mutation you're referring to. If you describe the mutation or provide details, I can help identify the type of mutation, such as point mutation, insertion, deletion, or frameshift.
A frameshift mutation in the CARD15 gene
A one base left out mutation is called a deletion mutation. This type of mutation involves the loss of one or more nucleotides from a DNA sequence, which can lead to a frameshift mutation if not in multiples of three.
Point Mutation is the mutation that involves a single or few nucleotide. This type of mutation replaces a single nucleotide to another.
Deletion Mutation causes DiGeorges Syndrome.
supposedly they are similar but mutation is more monster/alien type.