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Founder mutations are placed in this category but are unusual. This means that the mutation is not similar to any other mutation (Drayna 2006). Typical mutations affect people the same way but the damage to the gene is not the same in everyone. Founder mutations on the other hand have DNA damage that is identical to the founder. The DNA that is shared among people with a founder mutation is called a haploytpe (Drayna 2006). According to Drayna (2006) founder mutations can be easily passed on from generation to generation because carriers of the mutation lack symptoms. This results in millions of people not knowing that they may pass on a deadly disease to their offspring...
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