SNPY - Single Nucleotide Polymophism on Y Chromosome Reference Database 
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(expand all) • (collapse all)
+ Y 
+ A 
• A1 
+ A2 
• A2a 
• A2b 
+ A3 
• A3a 
+ A3b 
• A3b1 
+ A3b2 
• A3b2a 
• A3b2b 
+ BR 
+ B 
+ B1 
• B1a 
+ B2 
+ B2a 
+ B2a1 
• B2a1a 
+ B2a2 
• B2a2a 
+ B2b 
• B2b1 
• B2b2 
+ B2b3 
• B2b3a 
+ B2b4 
• B2b4a 
• B2b4b 
+ CR 
+ C 
• C1 
+ C2 
• C2a 
• C2b 
+ C3 
• C3a 
• C3b 
• C3c 
• C3d 
+ C4 
• C4a 
• C4b 
• C5 
+ DE 
+ D 
• D1 
+ D2 
+ D2a 
+ D2a1 
• D2a1a 
• D2a1b 
• D2a2 
• D3 
• D4 
+ D5 
• D5a 
+ E 
+ E1 
• E1a 
+ E2 
• E2a 
+ E2b 
+ E2b1 
• E2b1a 
+ E3 
+ E3a 
• E3a1 
• E3a2 
• E3a3 
• E3a4 
• E3a5 
• E3a6 
+ E3a7 
• E3a7a 
+ E3a8 
• E3a8a 
+ E3b 
+ E3b1 
+ E3b1a 
+ E3b1a1 
• E3b1a1a 
• E3b1a1b 
+ E3b1a2 
• E3b1a2a 
+ E3b1a3 
• E3b1a3a 
• E3b1a3b 
+ E3b1b 
• E3b1b1 
• E3b1b2 
+ E3b1c 
+ E3b1c1 
• E3b1c1a 
• E3b1c1b 
• E3b1d 
• E3b1e 
• E3c 
+ F 
• F1 
• F2 
+ G 
+ G1 
• G1a 
+ G2 
+ G2a 
• G2a1 
• G2b 
• G3 
• G5 
+ H 
+ H1 
+ H1a 
• H1a1 
• H1a2 
• H1a3 
• H1b 
• H2 
+ IJ 
+ I 
+ I1 
+ I1a 
• I1a1 
• I1a2 
• I1a3 
• I1a4 
+ I1b 
• I1b1 
+ I1b2 
• I1b2a 
+ I1c 
• I1c1 
• I1c2 
+ J 
+ J1 
• J1a 
• J1b 
• J1c 
• J1d 
• J1e 
+ J2 
• J2a 
• J2b 
• J2c 
• J2d 
+ J2e 
+ J2e1 
• J2e1a 
• J2e1b 
+ J2e1c 
• J2e1c1 
+ J2f 
+ J2f1 
• J2f1a 
• J2f2 
• J2g 
• J2h 
• J2i 
• J2j 
• J2k 
• J2l 
+ K 
+ K1 
• K1a 
+ K2 
• K2a 
• K3 
• K4 
+ K5 
+ K5a 
• K5a1 
• K6 
• K7 
+ L 
• L1 
+ L2 
• L2a 
• L2b 
+ L3 
• L3a 
+ M 
• M1 
+ M2 
+ M2a 
• M2a1 
• M2a2 
+ NO 
+ N 
• N1 
• N2 
+ N3 
+ N3a 
• N3a1 
+ O 
+ O1 
+ O1a 
• O1a1 
• O1a2 
+ O2 
+ O2a 
+ O2a1 
• O2a1a 
+ O2b 
• O2b1 
+ O3 
+ O3a 
• O3a1 
• O3a2 
+ O3a3 
• O3a3a 
+ O3a4 
+ O3a4a 
• O3a4a1 
• O3a4a2 
• O3a4b 
+ O3a5 
+ O3a5a 
• O3a5a1 
• O3a6 
• O3a7 
+ P 
+ Q 
+ Q1 
• Q1a 
• Q2 
+ Q3 
• Q3a 
• Q3b 
• Q3c 
• Q4 
• Q5 
+ R 
+ R1 
+ R1a 
+ R1a1 
• R1a1a 
• R1a1b 
• R1a1c 
+ R1b 
+ R1b1 
• R1b1a 
• R1b1b 
+ R1b1c 
• R1b1c1 
• R1b1c2 
• R1b1c3 
• R1b1c4 
• R1b1c5 
• R1b1c6 
• R1b1c7 
• R1b1c8 
+ R1b1c9 
• R1b1c9a 
• R1b1d 
• R2 

D2

 — Edit • New

Created at August 31st, 2007 | Modified at October 31st, 2007 | Validated at October 31st, 2007 | Curator
 

Markers

 — New

  • 12f2.2 aliased by 12f2b (Rosser et al. 2000) — Show details • Edit
    Mutation type: INS 500bp
    Rosser ZH., Zerjal T., Hurles ME., Adojaan M., Alavantic D., Amorim A., Amos W., Armenteros M., Arroyo E., Barbujani G., Beckman G., Beckman L., Bertranpetit J., Bosch E., Bradley DG., Brede G., Cooper G., Real C., Knijff D., Decorte R., Dub (2000), 'Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language.', Am J Hum Genet 67(6), 1526-43 (Rosser et al. 2000)
  • M64.1 aliased by M64a (Underhill et al. 2001) — Show details • Edit
    Mutation type: SNP A/G
    Underhill PA., Passarino G., Lin AA., Shen P., Lahr M., Foley RA., Oefner PJ., Sforza C. (2001), 'The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations.', Ann Hum Genet 65(Pt 1), 43-62 (Underhill et al. 2001)
  • M55 (Underhill et al. 2001) — Show details • Edit
    Mutation type: SNP T/C
    Underhill PA., Passarino G., Lin AA., Shen P., Lahr M., Foley RA., Oefner PJ., Sforza C. (2001), 'The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations.', Ann Hum Genet 65(Pt 1), 43-62 (Underhill et al. 2001)
  • M57 (Underhill et al. 2000) — Show details • Edit
    Mutation type: INS A
    Underhill PA., Shen P., Lin AA., Jin L., Passarino G., Yang WH., Kauffman E., Tamir B., Bertranpetit J., Francalacci P., Ibrahim M., Jenkins T., Kidd JR., Mehdi SQ., Seielstad MT., Wells RS., Piazza A., Davis RW., Feldman MW., Sforz C. (2000), 'Y chromosome sequence variation and the history of human populations.', Nat Genet 26(3), 358-61 (Underhill et al. 2000)
  • M179 (Underhill et al. 2001) — Show details • Edit
    Mutation type: SNP C/T
    Underhill PA., Passarino G., Lin AA., Shen P., Lahr M., Foley RA., Oefner PJ., Sforza C. (2001), 'The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations.', Ann Hum Genet 65(Pt 1), 43-62 (Underhill et al. 2001)
  • P37.1 aliased by P37a (Hammer et al. 2001) — Show details • Edit
    Mutation type: Unknown
    Hammer MF., Karafet TM., Redd AJ., Jarjanazi H., Benerecetti S., Soodyall H., Zegura SL. (2001), 'Hierarchical patterns of global human Y-chromosome diversity.', Mol Biol Evol 18(7), 1189-203 (Hammer et al. 2001)
  • P41.1 aliased by P41a (Hammer et al. 2001) — Show details • Edit
    Mutation type: Unknown
    Hammer MF., Karafet TM., Redd AJ., Jarjanazi H., Benerecetti S., Soodyall H., Zegura SL. (2001), 'Hierarchical patterns of global human Y-chromosome diversity.', Mol Biol Evol 18(7), 1189-203 (Hammer et al. 2001)
  • P12 — Show details • Edit
    Mutation type: Other
 

References


  • Jobling MA., Smith T. (2003), 'The human Y chromosome: an evolutionary marker comes of age.', Nat Rev Genet 4(8), 598-612 (Jobling & Smith 2003)


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