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What else can I help you with?
What are different types of mutation?
Deletion, insertion, inversion, translocation, and duplication [for the ppl. Who dnt kno!!]
Why does an insertion mutation usually cause defects during protein synthesis than a point mutation?
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.
What is an mutation?
An Inversion mutation is a mutation that causes a reversal in the order of a segment of a chromosome within the chromosome, or a gene.
What is an inversion mutation?
An inversion in meteorology is when atmospheric pressure causes an abnormal condition. An example would be that the pressure causes warmer air to sink closer to earth's surface and cooler air to rise higher. When this inversion happens, one of the effects is that pollution and smog stay trapped within our atmosphere.
Is hemophilia a insertion mutation?
Maybe
What mutation involves two chromosomes?
Inversion and duplication!
When a child is born with a chromosomal mutation when did the mutation occurs?
during meiosis
Which is not a frameshift mutation substitution insertion deletion or point mutation?
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.
What is insertion?
Insertion is a genetic mutation when an extra base is added to the DNA before or during replication
Why does an insertion mutation usually cause more defects in protein synthesis than a point mutation?
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.
What are two types of mutation?
From another angle: beneficial and detrimental.
What is the mutation in hemophilia?
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.
