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Blood cell
a) blood cell
Sperm cell
Yes, a point mutation will cause the cell to make an incompelete polypeptide chain that is non-functional, if the mutation results in a stop codon. This type of a mutation is also called as the Nonsense Mutation.
Nondisjunction, or sending both chromosomes to one cell during meiosis.
Depends on how likely the mutation is to occur (how dominate) and on the genetics of the other parent. If the offspring is a clone, the mutation will be passed from parent to clone.
a) blood cell
Blood cell
Sperm cell
Yes, a point mutation will cause the cell to make an incompelete polypeptide chain that is non-functional, if the mutation results in a stop codon. This type of a mutation is also called as the Nonsense Mutation.
Mutations in the hemoglobin molecules cause sickle cell anemia.
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.
Generally, a germ line mutation or sex cell mutation. Could be anything from a point mutation, one amino acid difference, to a whole frame shift mutation.
Yes because the breast tissue is undergoing cell differentiation.
It can't. A new mutation in a somatic cell will not influence the genetic composition of the progeny except in cases where the mutation affects the carrying out of reproduction. This is because the gametes (ova or sperm) only come from the reproductive tissue (ovaries, seminiferous tubule in the testes). we need something a 6th 7th and 8th graders teachers will believe we did ourselves please from me the person who thinks
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/