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[QUOTE]Originally posted by Ish Gebor: [QB] [QUOTE]Originally posted by capra: [qb] what part of this are you not getting? the forefather of CT inherited most of his mutations from BT, those are shared with B. the forefather of BT inherited most of his mutations from A2-T, those are shared with A2 and A3. the forefather of A2-T inherited most of his mutations from A1a-T, those are shared with A1a. and so on. the same mutations are passed on all the way to the present. you and i both carry the mutations that occurred way back then. that's what the whole tree is based on, which mutations are shared and which aren't. [/qb][/QUOTE]What part I'm not getting? I tell you it was already present in the population with in that region. Phylogenetic Mapping Most of the mutations here analyzed belong to the African portion of the MSY phylogeny, which is comprised of haplogroups A1b, A1a, A2, A3 and B [16]. Through phylogenetic mapping it was possible to identify 15 new African haplogroups and to resolve one basal trifurcation (Figure 1). A new deep branch within the ‘‘out of Africa’’ haplogroup C was also identified (Figure S1). Haplogroup A1b. The P114 mutation, which defines haplogroup A1b according to Karafet et al. [14], had been detected in central-western Africa at very low frequencies (in total, three chromosomes from Cameroon) [16,19]. These are the forefather who carried the mutation for R, before it left Africa. [/QB][/QUOTE]
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