Maybe
Hemophilia is a mutation of either of the genes that make factor VII or IX. Hemophilia A is a mutation of the F8 gene and Hemophilia B is the mutation of the F9 gene. Both of these mutations occur on the sex-linked X chromosome.
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.
Hemophilia is a genetic mutation of the sex-linked X chromosome.
Insertion mutations can affect many amino acids in the protein.An insertion mutation usually causes more defects during protein synthesis than point mutation because an insertion mutation will affect many amino acids in the protein.
A carrier for hemophilia is a female who carries the genetic mutation for hemophilia on one of her X chromosomes, but does not exhibit symptoms of the condition herself. Carriers can pass on the gene mutation to their children, resulting in hemophilia in male offspring. Testing can confirm carrier status.
A point mutation is not a frameshift mutation. Point mutations involve changes in a single nucleotide base, while frameshift mutations involve the insertion or deletion of nucleotide bases, causing a shift in the reading frame of the genetic code.
No, hemophilia is a genetic disorder caused by a mutation in the genes responsible for blood clotting, and it is not directly caused by inbreeding. Inbreeding can increase the likelihood of inheriting genetic disorders, including hemophilia, if the mutation is present in the family's gene pool.
Insertion is a genetic mutation when an extra base is added to the DNA before or during replication
Insertion mutations can affect many amino acids in the protein.An insertion mutation usually causes more defects during protein synthesis than point mutation because an insertion mutation will affect many amino acids in the protein.
From another angle: beneficial and detrimental.
They are both mutations of chromosomes
An insertion/deletion event.