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 

C

 — Edit • New

Created at August 19th, 2007 | Modified at November 1st, 2007 | Validated at October 30th, 2007 | Curator
 

Markers

 — New

  • M130 aliased by RPS4Y (Underhill et al. 2001, Vallone & Butler 2004) — 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)
    Vallone PM., Butler JM. (2004), 'Y-SNP typing of U.S. African American and Caucasian samples using allele-specific hybridization and primer extension.', J Forensic Sci 49(4), 723-32 (Vallone & Butler 2004)
  • M216 (Underhill et al. 2001, Brion et al. 2005) — 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)
    Brion M., Sanchez JJ., Balogh K., Thacker C., Verea B., Borsting C., Bellinghausen S., Bogus M., Court S., Schneider PM., Carracedo A., Morling N. (2005), 'Introduction of an single nucleodite polymorphism-based "Major Y-chromosome haplogroup typing kit" suitable for predicting the geographical origin of male lineages.', Electrophoresis 26(23), 4411-20 (Brion et al. 2005)
 

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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