genetic drift....
it is either
A. a genetic disorder
B. death
C. no change at all
microevolution
A point mutation is a genetic mutation when a wrong nucleotide bonded to DNA during replication. Usually, DNA polymerase can prevent that because it's an enzyme that finds the right nucleotides to bond to new DNA strands.
by what protocol we can mutate a single gene from leishmania BY ANOTHER PERSON - The answer is POINT mutation. I'm doing the worksheet too LOL hahah everyone is doing miggis homework huh === Too bad I can't find the rest of the answers for that homework D: But yea it is Point Some genetic disorders result when a mutation causes the product of a single gene to be altered or missing. ~From my science book o-o lol
If one base in a codon was changed, this would be a point mutation. This may not cause any change in the structure of the protein, or it could be severely damaging. Since most amino acids have more than one codon, it's possible that the mutation would result in one of the other codons for that amino acid. In that case, there would be no change in the sequence of amino acids, and no change in the structure or function of the protein. A point mutation might also result in a codon that codes for a totally different amino acid, which can cause a genetic disorder. One example of a genetic disorder caused by a point mutation is sickle cell anemia. It's also possible that the point mutation could cause the codon to code for a stop signal. Please read the article in the related links for more information.
false, point mutation is the change in any single base within DNA at a given time.it occurs only once during a single mutation
genetic variation originates from mutations on which evolution depends on.
genetic drift....
A mutation, usually a point mutation (where a single 'letter' in the genetic code is changed).
frameshift mutation: deletion
A mutation
Point mutation: single nucleotide is replaced with another. ex: sickle cell anemia.
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.
A genetic mutation is a change in a single or several base pair nucleotides in a DNA or RNA molecule. Mutations arise due to random errors during cell replication, as well as mutagens, which are mutation inducing physical or chemical agents.
A mutation
A mutation
If one base in a codon was changed, this would be a point mutation. This may not cause any change in the structure of the protein, or it could be severely damaging. Since most amino acids have more than one codon, it's possible that the mutation would result in one of the other codons for that amino acid. In that case, there would be no change in the sequence of amino acids, and no change in the structure or function of the protein. A point mutation might also result in a codon that codes for a totally different amino acid, which can cause a genetic disorder. One example of a genetic disorder caused by a point mutation is sickle cell anemia. It's also possible that the point mutation could cause the codon to code for a stop signal. Please read the article in the related links for more information.
A point mutation is a genetic mutation when a wrong nucleotide bonded to DNA during replication. Usually, DNA polymerase can prevent that because it's an enzyme that finds the right nucleotides to bond to new DNA strands.
A mutation.