Bca1 Mutation Research Paper

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Mutations are a result of changes in the DNA sequences. These changes can happen as a point mutation, which is a change in one base pair of codons, or the can happen to an entire sequence of pairs or the breaking of pairs. Point mutations are substitution, insertion, and deletion. Another type of mutation is translocation, and this can occur in a chromosome or between different chromosomes. With a substitution mutation it can be one of 3 types. These types are nonsense, misssence, or silent. Some mutations are caused by exposure to radiation and due to certain medications and chemicals. If these mutations are within reproductive cells, they will be passed down to the next generation. They can inherit is as a recessive trait, a dominate trait, or get the recessive trait from both parents. If the mutation is dominate, the offspring will have the disease. This is also true if they inherit it from both parents. If it is only inherited as a recessive trait from one parent, then they will be a carrier and will pass it to their offspring. This mutation will pass through generations the same as a gene for eye color or height. The same is true for a helpful mutation, like the mutation for resistance to diseases, for stronger bones, or better color vision. …show more content…

It had the youngest age of diagnosis, the highest percentage of death. It also had the highest number of preventative oophorectomies. BRC2 had half the number of patients and less than a third of the death rate of BRCA1, With the patient number and the number of deaths, a woman has approximately a 1 in 5.5 patients chance of dying from breast cancer if she has the BRCA1

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