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To start off though, let me define founder mutations. Founder mutations are a special class of genetic mutations embedded in strands of DNA (deoxyribonucleic acid) that are strictly identical in all organisms that have the mutation.
Everyone who has a founder mutation has damaged DNA that is embedded in a larger strand of DNA, and, as previously mentioned, is a perfect copy of the founder. The shared section of DNA is called a haplotype. If you share a haplotype, then you share an ancestor, of whom is the founder. Studying haplotypes can calculate the date at which the mutation was formed. You’re probably wondering how this is possible...
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