Offaly - Kilkenny Clan O'Nolan: FTDNA Advanced Y-DNA Markers and 23andMe SNP Results for Paternal and Maternal Lineages FTDNA Panel: Kittler DYS385a/b (K) N-4 - 17-11 N-30 - 17-11 Panel 5 DYS724 N-4 - 36-40 N-30 - 36-40 DYS725 N-4 - 31-31-31-32 N-30 - 29-31-31-32 DYS413 N-4 - 23-23 N-30 - 22-23 DYF399X N-4 - 21t-24c-24.1t N-30 - 21t-24c-24.1t DYF408 N-4 - 188-188-8-15 N-30 - 188-188-8-15 DYS464X N-4 - 15c-15c-17c-17c N-30 - 15c-15c-17c-17c DYF401 N-4 - 15-17 N-30 - 15-17 DYF397 N-4 - 11-14-15-15 N-30 - 11-14-15-15 DYF411 N-4 - 11-11 N-30 - 11-11 DYF371X N-4 - 10c-12t-13c-14c N-30 10c-12t-13c-14c DYF385 N-4 - 10-11 N-30 - 10-11 Panel 6 DYS578 N-4 - 9 N-30 - 8 DYS472 N-4 - 8 N-30 - 8 DYS590 N-4 - 8 N-30 - 8 DYF395a/b N-4 - 15-16 N-30 - 15-16 DYS531 N-4 - 11 N-30 - 11 DYF406S1 N-4 - 10 N-30 - 10 DYS511 N-4 - 10 N-30 - 10 DYS537 N-4 - 10 N-30 - 10 DYS641 N-4 - 10 N-30 - 10 Panel 7 DYS450 N-4 - 8 N-30 - 8 DYS481 N-4 - 22 N-30 - 22 DYS520 N-4 - 20 N-30 - 20 DYS557 N-4 - 16 N-30 - 16 DYS534 N-4 - 15 N-30 - 15 DYS446 N-4 - 13 N-30 - 13 DYS425 N-4 - 12 N-30 - 12 DYS436 N-4 - 12 N-30 - 12 DYS444 N-4 - 12 N-30 - 12 DYS490 N-4 - 12 N-30 - 12 DYS594 N-4 - 10 N-30 - 10 Panel 8 DYS492 N-4 - 14 N-30 - 14 DYS487 N-4 - 13 N-30 - 13 DYS565 N-4 - 12 N-30 - 12 DYS617 N-4 - 12 N-30 - 12 DYS568 N-4 - 11 N-30 - 11 DYS572 N-4 - 11 N-30 - 11 DYS640 N-4 - 11 N-30 - 11 Panel 9 DYS494 N-4 - 9 N-30 - 9 DYS505 N-4 - 12 N-30 - 12 DYS533 N-4 - 12 N-30 - 12 DYS549 N-4 - 12 N-30 - 12 DYS589 N-4 - 12 N-30 - 12 DYS636 N-4 - 12 N-30 - 12 DYS556 N-4 - 11 N-30 - 11 DYS638 N-4 - 11 N-30 - 11 DYS522 N-4 - 10 N-30 - 10 DYS575 N-4 - 10 N-30 - 10 23andMe N-4 Paternal Haplogroup R1b1b2a1a2d* (R-U152) R1b1b2a1a2d* defining mutations N/A R1b1b2a1a2d defining mutations rs1236440 (S28) C T R1b1b2a1a2 defining mutations rs34276300 (P312) C A R1b1b2a1a defining mutations rs13304168 (L52) C T rs9785659 (P311) A G rs9786076 (L11) T C rs9786283 (P310) A C R1b1b2a1 defining mutations rs9786140 (L51) G A R1b1b2a defining mutations rs9785971 (L23) G A rs9785831 (L150) T https://www.familytreedna.com/advanced-snp-descriptions.aspx?SNP=L150 Marker Name: L150 Display Name: rs9785831 Ancestral: C Derived: T Phylogeny: a branch of L23. This means it would be downstream of L23 instead of being parallel to it. rs9786142 (L49) T A R1b1b2 defining mutations rs877756 (S3) T C rs9786153 (M269) T C R1b1b defining mutations rs9785702 (P297) G C R1b1 defining mutations rs150173 (P25) C A R1b defining mutations rs9786184 (M343) C A R1 defining mutations rs1118473 (P286) C T rs17307070 (P225) G T rs2032624 (M173) A C rs7067478 (P242) G A rs9785717 (P238) G A rs9785959 (P236) C G rs9786197 (P234) T C rs9786232 (P233) T G R defining mutations rs1558843 (M306) C A rs17249974 (P285) C A rs17307398 (P224) C T rs2032658 (M207) A G rs4481791 (P227) C G rs891407 (P280) C G rs9786261 (P232) G A rs9786915 (P229) G C P defining mutations rs17222419 (P228) C T rs17250992 (P226) C T rs17307656 (P282) A G rs17315758 (P281) A G rs2032631 (M45) G A rs2032635 (M74) G A rs2740981 (P244) G A rs3865828 (P283) C T rs4116821 (P284) C G rs4141564 (P243) A G rs8181264 (P239) G C rs895530 (P295) T G rs9785740 (P237) A G rs9786119 (P235) A G rs9786781 (P230) G A K defining mutations rs17250121 (P128) C T rs3853054 (P132) G T rs3900 (M9) C G rs9786043 (P131) C T I1 defining mutations i4000189 (P40) T I/J/K defining mutations rs9786139 (L15) A G rs9786714 (L16) G A F defining mutations i4000053 (P14) D I rs16980391 (P149) G A rs16980396 (P148) C T rs16980459 (P139) G A rs16980478 (P138) T C rs16980499 (P166) C T rs16980711 (P133) G A rs16981340 (P146) C T rs17174528 (P187) G T rs17842387 (P145) G A rs2032652 (M89) C T rs2032665 (M213) T C rs4589047 (P163) A T rs4988808 (P142) G A rs7067496 (M235) T G rs9306845 (P141) G A rs9306848 (P160) A C rs9785905 (P159) C A rs9785908 (P136) T G rs9785913 (P158) C T rs9786095 (P157) T C rs9786502 (P135) C T rs9786636 (P140) G C rs9786707 (P151) T C rs9786877 (P134) C G C/F defining mutations rs4141886 (P143) G A C/T defining mutations i4000227 (P9.1) C A rs2032595 (M168) C T rs9341317 (M294) C T B/T defining mutations i4000077 (M139) I D rs13447347 (M299) T G rs2032630 (M42) A T rs2032647 (M94) C A Presence of one copy of the deltaE302 DYT1 mutation indicates the possibility of primary torsion dystonia, but not all carriers actually exhibit symptoms of the disease. Can pass mutation to offspring. New SNP: 23andMe v3 - Nolen (U152, Upgrade, rs7892842+) http://www.nature.com/nature/journal/v463/n7282/full/nature08835.html Ancient human genome sequence of an extinct Palaeo-Eskimo http://projects.binf.ku.dk/Palaeo-eskimo/full-genotyping/chrY.diff.annotation Palaeo - Eskimo Full Genotyping Y Chromosome chrY 3334922 C n AA 6.7938e-16 7-HATS P3.LTR.ERV1 8836 rs7892842 singles + AC Maternal Haplogroup I3 mtDNA I3 defining mutations rCRS=152 i3001922 C rCRS=207 i3002166 rCRS=239 i3000595 C rCRS=16086 i3001574 C I defining mutations rCRS=10034 rs41347846 rCRS=10034 i3001500 rCRS=16129 i4990110 rCRS=16129 i3001531 rCRS=16129 i3001605 rCRS=16391 rs34301918 rCRS=16391 i3001539 N1e'I defining mutations rCRS=250 rs41400048 rCRS=4529 i3002172 rCRS=8251 rs3021089 rCRS=15924 rs2853510 N1a'e'I defining mutations rCRS=10398 rs2853826 rCRS=15043 rs28357684 rCRS=15043 i3001344 N1a'd'e'I defining mutations rCRS=199 i3002111 N1a'c'd'e'I defining mutations rCRS=204 rs3135032 rCRS=204 i3002149 rCRS=204 i3002158 rCRS=13780 rs41358152 rCRS=13780 i3001513 N1 defining mutations rCRS=10238 rs28358275 rCRS=12501 rs28397767 N1'5 defining mutations rCRS=1719 rs3928305 N defining mutations rCRS=8701 i3000759 rCRS=8701 rs34488815 rCRS=9540 rs2248727 rCRS=9540 i3001497 rCRS=10398 rs2853826 rCRS=10873 rs2857284 rCRS=15301 rs28573847 rCRS=15301 i3001523 L3 defining mutations rCRS=769 rs2853519 rCRS=769 i3001949 rCRS=1018 rs2856982 rCRS=1018 i3001452 L3'4 defining mutations rCRS=182 rs41473347 rCRS=182 i3001445 rCRS=3594 rs2854134 rCRS=7256 rs28625947 rCRS=13650 rs2854123 rCRS=16278 rs41458645 rCRS=16278 i3001790 L3'4'6 defining mutations rCRS=4104 rs1117205 rCRS=7521 i1000010 rCRS=7521 i3001488 L2'3'4'6 defining mutations rCRS=195 rs2857291 rCRS=195 i3002066 rCRS=247 rs41334645 rCRS=247 i3001448 rCRS=825 rs2853520 rCRS=8655 rs2853822 rCRS=8655 i3002650 rCRS=10688 rs2853488 rCRS=10810 rs28358282 rCRS=10810 i3000954 rCRS=13105 rs2853501 rCRS=13506 rs2857287 rCRS=15301 rs28573847 rCRS=15301 i3001523 rCRS=16129 i4990110 rCRS=16129 i3001531 rCRS=16129 i3001605 rCRS=16187 i4000590 rCRS=16187 i4000591 rCRS=16189 rs28693675 rCRS=16189 i4000587 L2-6 defining mutations rCRS=152 i3001922 rCRS=2758 rs2856980 rCRS=2885 rs2854130 rCRS=7146 rs28546855 rCRS=8468 rs1116907 rCRS=8468 i3000730 L1-6 defining mutations rCRS=146 i3001869 rCRS=182 rs41473347 rCRS=182 i3001445 rCRS=4312 i3002160 rCRS=10664 rs2854121 rCRS=10915 rs2857285 rCRS=11914 rs2853496 rCRS=13276 rs2853502 rCRS=16230 rs2853514