All the sequences before the N* point have C10873T and after it 12705A. Several haplogroups branch off at the N* point:- There are pages for Haplogroups 'A', 'I and N', 'W', 'X' & 'Y'. There are also several sequences that come from close to the N* point, for these see:- the N* chart, the N* Asian page, the N* Far Eastern page, the Haplogroup P page, the Haplogroup S page, and sequences near the N* point and not found on the other pages: 1. Ingman_gyll A6.JS AY289056(Australian) 2. Ingman_gyll A8.JS AY289058(Australia) 3. Palanichamy A56.JS AY714031(India) 4. Hunjasgov A1.JS EF495214(Australia) The sequences have these differences from the CRS: - for the main stem leading from H: A73G A263G A750G A1438G A2706G A4769G C7028T A8860G G11719A C12705T C14766T A15326G C16223T T16519C and excluding changes at 309 and 315, and at 16183 & 16193 the mutation lists are: 1. Ingman_gyll A6.JS AY289056(Australian) T152C C509T C1628T G5460A G5563A T6221C G6755A C9140T A10700G T15300C A15326G T15852C C15885T A15924G G16213A G16303A T16362C 2. Ingman_gyll A8.JS AY289058(Australia) T152C C509T G5460A G5563A T6221C G6755A C9140T A10700G T15300C T15852C C15885T A15924G G16213A G16274A G16303A T16362C 3. Palanichamy A56.JS AY714031(India) G1719A T5063C T6011C C6164T A7076G C7492T G8545A A9545G A10232G T11626C A13434G C14533T T15262C T15972C A16051G T16092C C16111T G16129A T16311C 4. Hunjasgov A1.JS EF495214(Australia) T146C T152C A178G T195C G2831A G3483A T4967C C5300T C5704T T6896C A8631G T10101C A11020G G13135A A13263G A16066G A16177G T16189C A16240G C16261T C16290T T16311C