Haplogroup CT (Y-DNA)

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Haplogroup CT
Time of origin 31 to 55 thousand years BP
Place of origin Africa
Ancestor BT
Descendants CF, DE
Defining mutations P9.1, M168 and M294

In human genetics, Haplogroup CT (P9.1, M168, M294) is a Y-chromosome haplogroup.

Haplogroup CT contains the M168 change, which is present in all Y-chromosome haplogroups except A and B and is therefore the common ancestral type of all early migration out of Africa as per the Single origin hypothesis. The mutation is believed to have occurred 31 to 55 thousand years before present within North East Africa.[1]


[edit] Origins

The defining mutations separating CT (all haplogroups excepting A and B) are P9.1, M168 and M294. These mutations predate the "Out of Africa" migration. The defining mutations of DE probably occurred in Northeastern Africa some 50,000 years ago. The M130 and M216 mutations that distinguish Haplogroup C from all other descendants of CR may have occurred somewhat later, perhaps even as early as 48,500 years ago, after the first Out of Africa migration brought Homo sapiens to the southern coast of Southwest Asia.[2]

[edit] Subclades

[edit] References

  1. ^ ISOGG
  2. ^ Reddy, B. Mohan; B. T. Langstieh, Vikrant Kumar, T. Nagaraja, A. N. S. Reddy, Aruna Meka, A. G. Reddy, K. Thangaraj, Lalji Singh (2007-11-7). "Austro-Asiatic Tribes of Northeast India Provide Hitherto Missing Genetic Link between South and Southeast Asia". PLoS ONE 2 (11). doi:10.1371/journal.pone.0001141. PMID 17989774. 


Human Y-chromosome DNA (Y-DNA) haplogroups (by ethnic groups, famous haplotypes)

most recent common Y-ancestor
|
A BT
B CT
DE CF
D E C F
G H IJ K
I J L M NO P S T
N O Q R
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