Haplogroup L0k is one of the subgroups of Haplogroup L0. The details of the sequences are: 1. Ingman A46.JS AF347008(San) 2. Ingman A47.JS AF347009(San) Changes from CRS of: A73G G247A A263G A750G G769A T825A G1018A G1048A A1438G A2706G G2758A T2885C C3594T C3516A A4104G C4312T A4769G A4793G T5442C C7028T A7146G C7256T G7521A C8468T C8655T A8701G A8860G T9540C A10398G G10688A T10810C T10873C G11719A G11914A C12705T A13105G C13506T C13650T C14766T A15326G C16223T T16519C For L0 T6185C C9042T A9347G G9755A G10589A C10664T T10915C G12007A A12720G A13276G And for L0k T4586C C9818T - variable changes at 309 and 315 - variable changes at 522-523. 1. Ingman A46.JS AF347008(San) L0k T146C T152C A189G T195C C198T T204C G207A T850C T1243C C2650T C2836A G4541A T4586C T4907C A5811G C6938T A7257G A7673G G8251A T8911C G8994A C9042T A9136G A9347G C9818T A10499G G10589A C10664T A10876G T10915C C10920T C10939T C11296T T11299C A11653G G12007A G12070A T13020C A13276G G13590A T13819C G13928C T14020C T14182C T14371C T14374C A16166C T16172C T16189C 16193.C T16209C C16214T A16230G C16278T C16291G T16311C 2. Ingman A47.JS AF347009(San) L0k T146C T152C A189G T195C C198T G207A T850C T1243C A2060G C2836A G4541A T4586C T4907C A5811G C6938T A7257G G7347A G8292A T8911C G8994A C9042T A9136G A9347G C9818T A10499G G10589A C10664T A10876G T10915C C10920T C10939T C11296T T11299C A11653G G12007A G12070A T13020C A13276G G13590A T13819C G13928C T14020C T14182C T14371C T14374C A16166. 16169.C T16172C C16187T T16189C T16209C C16214T A16230G C16278T C16291G T16311C A30.JS EF184609(S. Africa) Haplogroup L0k Ile.. C4312T Ser(UCN).. G7457C Asp.. G7521A A73G T146C T152C A189G T195C C198T G207A G247A 315.C C522. A523. A750G G769A T825A T850C G1018A C1048T T1243C A1438G A2706G G2758A C2836A T2885C C3107N T3338A C3516A C3594A T3653A A4104G C4312T G4541A A4769G T4907C T5442C T6185C C6938T C7028T G7457C G7521A C8468T C8655T A8701G A8860G T8911C G8994A C9042T A9136G A9347G T9540C C9818T A10398G A10499G G10589A C10664T G10688A A10765T A11653G G11719A G11914A G12007A T13020C A13105G A13276G C13420T T14371C T14374C A16166C C16187T T16189C T16209C C16214T C16223T A16230G C16278T C16291G T16311C T16519C A31.JS EF184610(S. Africa) Haplogroup L0k Ile.. C4312T Cys.. A5811G Asp.. G7521A A73G T146C T152C A189G T195C C198T G207A G247A 309.C 315.C C522. A523. A750G T825A T850C G1018A C1048T T1243C A1438G A2363G A2706G G2758A C2836A T2885C C3107N C3516A C3594T A4104G C4312T G4541A T4586C A4769G T4907C A5811G T6185C C6938T C7028T A7146G C7256T A7257G G7521A C8468T C8655T A8701G A8860G T8911C G8994A C9042T A9136G A9347G T9540C C9818T A10398G A10499G G10589A C10664T G10688A C10727G T10810C T10873C A10876G T10915C C10920T C10939T C11296T T11299C A11653G G11719A G11914A T11988C G12007A G12070A T13020C A13105G A13276G C13506T G13590A C13650T T13819C G13928C T14182C T14371C T14374C G14569A C14766T A15326G A15788. C15789. C15790. A15791. T15792. A16166C T16172C C16187T T16189C T16209C C16223T A16230G C16278T C16291G T16311C T16519C A32.JS EF184611(S. Africa) Haplogroup L0k Ile.. C4312T Cys.. A5811G Asp.. G7521A A73G T146C T152C A189G T195C C198T T204C G207A G247A 309.C 315.C C522. A523. A750G G769A T825A T850C G1018A C1048T T1243C A1438G A2706G G2758A C2836A T2885C C3516A C3594T A4104G C4312T G4541A T4586C A4769G T4907C T5442C A5811G T6185C C6938T C7028T A7146G C7256T A7257G G7521A G8251A C8468T C8655T A8701G A8860G T8911C G8994A C9042T A9136G A9347G T9540C C9818T A10398G A10499G G10589A C10664T G10688A T10810C T10873C A10876G T10915C C10920T C10939T C11296T T11299C A11653G G11719A G11914A G12007A G12070A C12705T T13020C A13105G A13276G C13506T G13590A C13650T T13819C G13928C T14020C T14182C T14371C T14374C C14766T A15326G A16166C T16172C C16187T T16189C T16209C C16214T C16223T A16230G C16278T C16291G T16311C T16519C