The entire work is identified by the Version Number and date given on the
Main Page. Directions for citing the document are given at
the bottom of the Main Page.
Version History Last
revision date for this specific page: 26 November 2014
Because of continuing research, the structure of the Y-DNA Haplogroup Tree changes and ISOGG does its best to keep the tree updated with the latest developments in the field. The viewer may observe other versions of the tree on the Web. Email Alice Fairhurst if the differences need clarification or if you find any broken links on this page.
LINKS: Main Page Y-DNA Tree Trunk SNP Index Papers/Presentations Cited Glossary Listing Criteria |
CLADE/SUBCLADE SYMBOLS: Added Redefined |
SNP SYMBOLS: Not on 2013 tree Confirmed within subclade Provisional Private Investigation |
The criteria for a representative SNP printed in bold for a subclade is: traditional usage, testing one in multiple labs, and/or being found in the area of the chromosome used in recent research studies.
SNPs listed below in italics (colored black or red) are quality variants from next-generation sequencing reports consistently showing as representing that subgroup.
Contact Person for Haplogroup G: Ray H. Banks
G M201/PF2957, CTS34/M3442/PF2780, CTS175/M3226/PF2782,
CTS189/M3444, CTS282/M3445, CTS373/M3448, CTS440/M3233/PF2842, CTS635/M3449/PF2843, CTS670/M3451, CTS692/M3452,
CTS827/M3454/PF2847, CTS995/M3455, CTS1010/PF2848, CTS1013/M3242/PF2849, CTS1029/M3456/PF2850, CTS1139/M3458/PF2852,
CTS1283/M3461/PF2855, CTS1437/M3462/PF2856, CTS1574, CTS1577/M3499/PF2922, CTS1612/M3500/PF2923,
CTS1613/M3501/PF2924,
CTS1624/PF2925, CTS1750/PF2927, CTS1768/M3505/PF2928, CTS1997/M3508/PF2933, CTS2016.1/M3509.1/PF2934.1,
CTS2120/M3510/PF2935, CTS2125/M3511, CTS2126/M3512, CTS2136/M3513/PF2938, CTS2174/M3515/PF2939, CTS2215/M3287/PF2940,
CTS2251/M3289, CTS2271/M3516, CTS2357/M3517/PF2943, CTS2506/M3519/PF2945, CTS2517/M3520/PF2946, CTS2624/M3522,
CTS4101/M3526/PF2963, CTS4238/M3528/PF2966, CTS4479/PF2793, CTS4523/M3311/PF2974, CTS4613/M3532/PF2975,
CTS4749/M3534/PF2977, CTS4761/M3535/PF2978, CTS4887/M3536/PF2979, CTS5317/M3537, CTS5414/M3538/PF2981,
CTS5498/M3539/PF2982, CTS5504/M3322/PF2983, CTS5640/L1342/M3540, CTS5658/M3541/PF2985, CTS5699/M3542,
CTS5757/M3328/PF2989, CTS5837/M3543/PF2990, CTS6073/M3544/PF2992, CTS6483/M3547/PF2996, CTS6807/M3550,
CTS6894/PF3003, CTS6936/M3552/PF3004, CTS6957/M3553/PF3005, CTS7092/M3555/PF3006, CTS7269/M3557,
CTS7388/M3558/PF3009,
CTS7674/M3562/PF3015, CTS7929/M3563/PF3016, CTS8023/M3564/PF3017, CTS8531/M3565, CTS8717/M3566, CTS9011/M3567/PF3024,
CTS9190/M3568/PF3025, CTS9593/M3570, CTS9641/M3367/PF3030, CTS9707/M3571/PF3031, CTS9710/M3572/PF3032,
CTS9894/PF3036/M3574, CTS10026/PF3037/M3575, CTS10280/PF3039/M3577, CTS10393/PF3041/M3379, CTS10706, CTS10721/M3611,
CTS10723/M3612, CTS10824/M3613/PF3097, CTS10945/M3206, CTS11185/M3616/PF3100, CTS11228/M3618,
CTS11294/L769/PF3104, CTS11331/M3620, CTS11400/M3621/PF3106, CTS11529/M3622, CTS11670,
CTS11702/PF3111, CTS11907/M3424/PF3113, CTS11911/M3623/PF3114,
CTS12040/M3624/PF3115, CTS12309/PF3127, CTS12440/M3629/PF3126, CTS12600/M3630/PF3128, CTS12654/M3631/PF3129,
CTS12704/M3439/PF3130, CTS12731/M3632/PF3131, CTS12949/M3634/PF3132, CTS13035/PF3133, F2076/L524/PF3136,
F3359/M3614/PF3098, F3496/M3625/PF3118, L116/PF2955/S284, L154/PF3139, L204/PF2825, L269/PF3135,
L382/M3523/PF2951, L402, F1131/L519,
F1383/L520/PF2892, F1551/L521/PF2899,
L522/PF3011, F2906/L523/PF3027, L605/PF3023, L770, L836, L837, L1258, L1407/Z3439,
M3248/PF2859, M3257/PF2871, M3258/PF2872, M3264/PF2878, M3266/PF2881,
M3274/Z3218, M3387/PF3048, M3402/Z6110, M3432/PF3117, M3450/PF2844, M3459/Z3182, M3463/PF2857,
M3464/PF2858,
M3466/PF2861, M3468/Z3192, M3470/PF2865, M3471/PF2866, M3472/PF2867, M3473/PF2868, M3474/PF2869, M3476/PF2873,
M3477/PF2875, M3478/PF2876, M3479/PF2877, M3481/PF2880, M3482/PF2884, M3485/PF2888, M3486/PF2889, M3487/PF2890,
M3489/Z3215, M3490/PF2894, M3494/Z3226, M3495/PF2902, M3496/Z3229, M3497/Z3230, M3498/PF2921, M3502/Z3302,
M3507/PF2932, M3514/PF3265, M3560/PF3012, M3569/Z3401, M3580/PF3046, M3582/PF3049, M3583/PF3050, M3586/PF3053,
M3587/PF3054, M3588/PF3057, M3589/Z6108, M3591/PF3061, M3593/PF3063, M3595/PF3065, M3596/PF3068, M3597/PF3069,
M3598/Z3284, M3599/PF3070, M3600/PF3071, M3601/PF3072, M3603/PF3075, M3604/PF3076/S7530,
M3605/PF3077, M3606/Z3508,
M3608/PF3092, M3609/PF3094, M3619/PF3103, M3627/PF3121, M3628/PF3122, M3633/Z3561, P257/PF2950/U6,
Page94/PF3137/U17, PF2788, PF2790, PF2791, PF2796, PF2802, PF2804, PF2805.1/Z2540.2,
PF2806, PF2808, PF2809, PF2815, PF2816, PF2817, PF2819, PF2821, PF2831, PF2836, PF2837,
PF2901, PF2907, PF2908,
PF2910, PF2914, PF2915, PF2917, PF2918, PF2920, PF2952/S314/U2, PF2956/U3, PF2958/U7,
PF3022, PF3045, PF3067, PF3080, PF3083, PF3087, PF3088, PF3123, PF3343,
PF3134/U33, U12, U20,
U21, U23, Z3067, Z3078, Z3080, Z3081, Z3085, Z3087, Z3089/S8863/Y232, Z3094, Z3095, Z3097, Z3102, Z3104,
Z3117, Z3120, Z3122, Z3136, Z3144, Z3145, Z3150, Z3152, Z3166, Z3201, Z3239, Z3246, Z3247, Z3248, Z3250, Z3258/S1435,
Z3262, Z3285, Z3314, Z3349, Z3400, Z3438, Z3478, Z3482, Z3485, Z3502, Z3507, Z3539, Z6040, Z6106, Z6107, Z6115,
Z6121, Z6317, Z6318, Z6324, Z6325, Z6472
•
G* -
•
G1 M342, CTS5933, F858, F1218, F1354,
F2447, F2498, F2853, F3062, F4154, F4232, F4262, F4341, L833, M285, Z3176, Z3200,
Z3208, Z3231, Z3252, Z3308, Z3322, Z3327, Z3344, Z3393, Z3419, Z17860, Z17861, Z17862, Z17863, Z17864, Z17865, Z17866,
Z17867, Z17868, Z17869, Z17870, Z17872, Z17873
• •
G1* -
• •
G1a CTS11562, F1761, F2376, F4113,
F4297
• • •
G1a* -
• • •
G1a1 L1324, L1325, L1327, L1414
• • • •
G1a1* -
• • • •
G1a1a L201, L202, L203
• • • •
G1a1b L1323
• •
G1b L830, L831, L832, L834, L835
•
G2 P287/PF3140, CTS1491, CTS1492,
CTS1868/PF2929,
CTS1900/M3506/PF2931, CTS2406/M3518/PF2944, CTS2593/M3521/PF2947, CTS4136/M3527/PF2964, CTS4242/M3529/PF2967,
CTS4264/M3530/PF2968, CTS4413/M3531/PF2971, CTS4703/M3533/PF2976, CTS5666/M3325/PF2986, CTS6316/M3545,
CTS6692/M3548/PF2998, CTS6742/M3549/PF2999, CTS7430/M3559/PF3010, CTS7662/M3561/PF3014, CTS9885/M3573/PF3035,
CTS10089/M3576/PF3038, CTS11016/M3615/PF3099, CTS11196/M3617/PF3101, F744/M3229/PF2785,
F1189/M3267/PF2883, F1239/M3483/PF2886, F1294/M3484/PF2887, F1393/M3270/PF2893,
F1496/M3492, F1647/PF2904, F2319/L496/M3546/PF2995, F3070/M3578/PF3042, F3198/M3584, F3220/M3592, F3226/M3594/PF3064,
F3344/M3610/PF3095, F3536/M3626/PF3120, L79, L89/M3475/PF3138, L142.2,
L156/PF3002, M3273/PF2895, M3276/PF2903, M3446/PF2839, M3447/PF2840,
M3465/PF2860, M3469/PF2864, M3480/PF2879, M3488/PF2891, M3491/PF2897, M3493/PF2898,
M3581/PF3047, M3585/PF3052, M3607/PF3091, PF2787, PF2789, PF2792, PF2794, PF2797, PF2798,
PF2800, PF2803, PF2807, PF2810, PF2814, PF2820, PF2830, PF2835, PF2905, PF2909,
PF2912, PF3082, PF3093, PF3119, PF3125, Z3099, Z3042, Z3056, Z3060, Z3100, Z3112, Z3146, Z3237, Z3274, Z3303,
Z3499, Z3504, Z6023, Z6103/M3579, Z6105, Z6114, Z6292, Z6305, Z6474
• •
G2* -
• •
G2a P15/PF3112, CTS32/PF2779, CTS211/M3227/PF2783,
CTS1879/PF2930, CTS5416/M3320, CTS6026/M3331/PF2991, CTS6314/M3334, CTS6630/M3340/PF2997, CTS6753/M3342/PF3000,
CTS8673/M3358/PF3020, CTS9318/M3362/PF3026, CTS11463/M3421/PF3108, CTS11627/PF3110, F1554/PF2900, F1975/PF2969/M3307,
F1980/M3309/PF2972, F2274/M3333/PF2993, F2301/M3335/PF2994, F2529/M3348/PF3013, F3088/PF3043, F3734/M3428/PF3116,
F4086/M3251/PF2863, L31/PF3142/S149, L149.1, L1341, M3393/PF3056, M3397/PF3060, M3401/PF3066,
M3408/PF3073, M3410/PF3078, PF2799, PF2833, PF2911, PF3034,
PF3079, PF3141/U5, Z3072, Z3113, Z3114, Z3154, Z3167, Z3240, Z3249, Z3506,
Z6138
• • •
G2a* -
• • •
G2a1 L293, FGC528/Z6528, FGC569/Z6710,
FGC570/Z6567, FGC571/Z6686, FGC572/Z6593, FGC573/Z6535, FGC574/Z6564, FGC576/Z6537, FGC577/Z6539, FGC578/Z6540,
FGC580/Z6526, FGC581/Z6527, FGC582/Z6543, FGC585/SK1113/Z6529, FGC586/Z6544, FGC587/Z6530, FGC588/Z6531, FGC589/Z6532,
FGC590/Z6533, FGC591/Z6534, FGC592/Z6546, FGC593/Z6548, FGC594/Z6707, FGC595/Z6553, FGC596/Z6554, FGC597/SK1109/Z6556,
FGC598/Z6559, FGC599/Z6655, FGC600/Z7993, FGC601/Z6709, FGC602/Z6562, FGC603/Z6565, FGC604/Z6568, FGC605/Z6569,
FGC606/SK1107/Z6570, FGC607/Z6571, FGC608/Z6572, FGC610/Z6681, FGC611/Z6684, FGC612/Z6573, FGC613/Z6574, FGC614/Z6575,
FGC616/SK1110/Z6577, FGC617/Z6578, FGC618/Z6579, FGC620/Z6580, FGC621/Z6583, FGC622/Z6584, FGC623/Z6585, FGC624/Z6586,
FGC625/Z6591, FGC626/Z6592, FGC628/Z6597, FGC630/Z6599, FGC631/Z6601, FGC632/Z6602, FGC633/Z6735, FGC634/Z6605,
FGC635/Z6738, FGC636/Z6607, FGC637/Z6608, FGC638/Z6609, FGC639/Z6610, FGC640/Z6611, FGC641/Z6612, FGC642/Z6613,
FGC644/Z6615, FGC655/Z6622, FGC666/Z6627, FGC673/Z6631, FGC682/Z6647, FGC688/Z6708, FGC739/Z6698, FGC754/Z6715,
FGC769/Z6737, FGC1027/Z6557, FGC1028/Z6604, FGC1050/Z8009, FGC1092/Z6538, FGC3753/Z6563, FGC3756/Z6618, FGC7528/Z6713,
FGC7530/Z6588, FGC7531/Z6551, FGC7533/Z6547, FGC7534/Z6590, FGC7535/SK1106/Z6552, FGC7536/Z6555, FGC7537/Z6545,
FGC7538/Z6566, FGC7540/Z6525, FGC7542/SK1112/Z6594, FGC7543/Z6589, FGC7544/Z6587, FGC7545/Z6561, FGC7546/Z6606,
FGC7547, FGC7581/Z6541, FGC7582/Z6719, FGC7583/Z6598, FGC7584/Z6581, M7635, PF1123, SK1115/Z6582, Z6600, Z6603,
Z16580
• • • •
G2a1* -
• • • •
G2a1a P16_1, P16_2, FGC645/Z6616,
FGC667/Z6628, FGC670/Z6629, FGC699/Z6671, FGC700/Z6672, FGC703/Z6674, FGC712/Z6676, FGC714/Z6678,
FGC727/Z6690, FGC741/Z6699, FGC757/Z6717, FGC759/SK1110/Z6718, FGC762/Z6725, FGC768/Z6736,
FGC771/Z6739
• • • • •
G2a1a* -
• • • • •
G2a1a1 FGC715/Z6679,
FGC701/Z16581, FGC733/Z6693, FGC1068/Z6595
• • • • •
•
G2a1a1* -
• • • • •
•
G2a1a1a Z6638, F3099,
FGC3797/Z8013, Z6632, Z6633, Z6634, Z6635, Z6637, Z6639, Z6640,
Z6643, Z6650, Z6654, Z6661, Z6670, Z6677, Z6687, Z6691, Z6692,
Z6694, Z6697, Z6706, Z6714, Z6720, Z6728, Z6734, Z8014
• • • • •
• •
G2a1a1a* -
• • • • •
• •
G2a1a1a1 Z7940, FGC692, FGC750/Z7962,
Z7956, Z7957, Z7958, Z7959, Z7960, Z7961, Z8008, Z8011
• • • • •
• • •
G2a1a1a1* -
• • • • •
• • •
G2a1a1a1a Z7941, Z7943
• • • • •
• • •
G2a1a1a1b FGC719
• • • • •
• • • •
G2a1a1a1b* -
• • • • •
• • • •
G2a1a1a1b1 Z7947,
FGC677, FGC681, FGC717, FGC718, FGC723, FGC729, FGC730, FGC745, FGC756, FGC767, FGC770, FGC775, FGC777,
Z7948
• • • • •
• •
G2a1a1a2 FGC1048/Z7953,
FGC1049/Z7954
• • • • •
•
G2a1a1b Z6673,
FGC1123, FGC1126, FGC1132, FGC1137, FGC1147, Z6642, Z6680, Z6705
• • • •
G2a1b Z17775, Z17774
• • •
G2a2 CTS4367/L1259/M3308/PF2970,
PF2824, PF2826
• • • •
G2a2* -
• • • •
G2a2a PF3146, PF3147, PF3151, PF3159, PF3161,
PF3165, PF3166, PF3167, PF3168,
PF3172, PF3175, PF3176, PF3180, PF3181, PF3182, PF3184, PF3185, PF3186, PF6827
• • • • •
G2a2a* -
• • • • •
G2a2a1 PF3177, PF3155, PF3160, PF3163,
PF3170, PF3171, S11510/Z6199, S11769/Z6201, S15710/Z6042, S17801/Z6286
• • • • •
•
G2a2a1* -
• • • • •
•
G2a2a1a M286
• • • • •
•
G2a2a1b L91/PF3246/S285
• • • • •
• •
G2a2a1b* -
• • • • •
• •
G2a2a1b1 PF3239, CTS3850/Z2051, FGC5668,
FGC5676, FGC5681, PF3231, PF3240, PF3247, Z6043, Z6123, Z6126, Z6129,
Z6130, Z6132, Z6200, Z6277, Z6283, Z6303, Z6312, Z6476,
Z6477, Z6486, Z6490, Z6492
• • • • •
• • •
G2a2a1b1* -
• • • • •
• • •
G2a2a1b1a L166, FGC5671, FGC5673, FGC5687, FGC5696,
FGC5721,
L167, PF3178, PF6846, Z1370.2, Z6134, Z6206,
Z6207, Z6209, Z6213, Z6215, Z6219, Z6220, Z6287,
Z6493, Z6499, Z6516, Z12228, Z12229, Z12230
• • • • •
• • • •
G2a2a1b1a* -
• • • • •
• • • •
G2a2a1b1a1 FGC5672
• • • •
G2a2b L30/PF3267/S126,
L32/PF3266/S148/U8, L190/M485, PF2811
• • • • •
G2a2b* -
• • • • •
G2a2b1 M406/PF3285M3249/PF3287,
M3268.1/PF3292.1, M3281/PF3297, M3312/PF3300, M3314/PF3301, M3323/PF3304, M3366/PF3312, M3382/PF3315,
M3423/PF3319
• • • • •
•
G2a2b1* -
• • • • •
•
G2a2b1a L14/Page57/S130/U16, L90/Page19/S133
• • • • •
•
G2a2b1b L645
• • • • •
•
G2a2b1c PF3296, PF3293,
PF3316
• • • • •
G2a2b2 CTS5762/Z1819, CTS1891/PF3264,
CTS2488, CTS8143/PF3324, CTS9605, CTS9957/PF3325, F2121/PF3323, L141.1, PF2818,
PF3275
• • • • •
•
G2a2b2* -
• • • • •
•
G2a2b2a P303/Page108/PF3340/S135/Z765, CTS688,
CTS946, CTS1949/PF3334/Z1820, CTS4454/PF3335,
CTS6719/PF3336/Z763, CTS10366/PF3338, CTS10725/PF3344, Page98/Z766, PF3329, PF3330,
PF3332, PF3333, PF3339, PF3342, Z3077, Z3084, Z3142,
Z3243, Z3481, Z6109, Z6136, Z6323
• • • • •
• •
G2a2b2a* -
• • • • •
• •
G2a2b2a1 L140/S316, CTS796, CTS12570, CTS12891/PF3347,
PF2823, PF3331, PF3337/Z764, PF3345, PF3346, Z3065, Z3155, Z3220,
Z3245, Z3351, Z3501, Z3517, Z6294
• • • • •
• • •
G2a2b2a1* -
• • • • •
• • •
G2a2b2a1a U1, Z6779
• • • • •
• • • •
G2a2b2a1a* -
• • • • •
• • • •
G2a2b2a1a1 L13/S131/U13, CTS4672/Z2013,
FGC947/Z2027, L78/M527, Z1993, Z2005
• • • • •
• • • • •
G2a2b2a1a1* -
• • • • •
• • • • •
G2a2b2a1a1a CTS9909/Z2022, CTS417/Z1991,
Z2014
• • • • •
• • • • •
•
G2a2b2a2a1a* -
• • • • •
• • • • •
•
G2a2b2a1a1a1 Z2003, Z2009
• • • • •
• • • • •
• •
G2a2b2a1a1a1* -
• • • • •
• • • • •
• •
G2a2b2a1a1a1a L1263
• • • • •
• • • •
G2a2b2a1a2 L1266, L654.2
• • • • •
• • • • •
G2a2b2a1a2* -
• • • • •
• • • • •
G2a2b2a1a2a L1264, L1265, L1268
• • • • •
• • •
G2a2b2a1b L497/S317, CTS1899/PF6851/Z738,
CTS7111/Z748,
PF6850/Z728, PF6852/Z754
• • • • •
• • • •
G2a2b2a1b* -
• • • • •
• • • •
G2a2b2a1b1 CTS9737/Z1815
• • • • •
• • • • •
G2a2b2a1b1* -
• • • • •
• • • • •
G2a2b2a1b1a Z725, CTS11352/Z759,
FGC469/Z16776, Z727, Z1817
• • • • •
• • • • •
•
G2a2b2a1b1a* -
• • • • •
• • • • •
•
G2a2b2a1b1a1 L43/S147
• • • • •
• • • • •
• •
G2a2b2a1b1a1* -
• • • • •
• • • • •
• •
G2a2b2a1b1a1a L42/S146
• • • • •
• • • • •
•
G2a2b2a1b1a2 CTS6796/Z726
• • • • •
• • • • •
• •
G2a2b2a1b1a2* -
• • • • •
• • • • •
• •
G2a2b2a1b1a2a CTS4803
• • • • •
• • • • •
• • •
G2a2b2a1b1a2a* -
• • • • •
• • • • •
• • •
G2a2b2a1b1a2a1 S2808
• • • • •
• • • • •
• • • •
G2a2b2a1b1a2a1* -
• • • • •
• • • • •
• • • •
G2a2b2a1b1a2a1a CTS10391, S23438
• • • • •
• • • • •
• • • •
G2a2b2a1b1a2a1b FGC14522
• • • • •
• • • • •
• • • •
G2a2b2a1b1a2a1c Z17780,
Z17783
• • • • •
• • • • •
• •
G2a2b2a1b1a2b Z16775
• • • • •
• • • • •
• • •
G2a2b2a1b1a2b* -
• • • • •
• • • • •
• • •
G2a2b2a1b1a2b1 Z16770, Z16771,
Z16672, Z16773, Z16777, Z17394
• • • • •
• • •
G2a2b2a1c CTS342
• • • • •
• • • •
G2a2b2a1c* -
• • • • •
• • • •
G2a2b2a1c1 Z724, CTS6325,
CTS8476/PF6867, Y367/Z3511, Y368/Z3512
• • • • •
• • • • •
G2a2b2a1c1* -
• • • • •
• • • • •
G2a2b2a1c1a CTS5990/Z1903, CTS77, CTS2073, CTS4472,
CTS6763, CTS7045, CTS7155, CTS7658, CTS11388, FGC287/Y370, PF6851, PF6863, PF6865,
PF6866, Z2047, Z2048, Z3033, Z3038, Z3040, Z3055,
Z3057, Z3064, Z3066, Z3073, Z3082, Z3133, Z3137, Z3139, Z3162, Z3171, Z3177, Z3193, Z3219, Z3234, Z3236, Z3263,
Z3265, Z3312, Z3332, Z3380, Z3381, Z3388, Z3396, Z3410, Z3423, Z3435, Z3440, Z3445, Z6140, Z6141,
Z6162, Z6296, Z6297, Z6319, Z6320, Z6321, Z6322, Z6521, Z6522, Z6524
• • • • •
• • • • •
•
G2a2b2a1c1a* -
• • • • •
• • • • •
•
G2a2b2a1c1a1 L640, CTS1934, CTS2762, CTS3426,
CTS9329, CTS12069, FGC333, FGC334/Y90, FGC335, FGC337, FGC338/Y74, FGC340,
FGC341, FGC346, FGC7497, FGC7499, Z3029, Z3294, Z3307, Z3315, Z3373, Z3434, Z3574, Z3576,
Z3577, Z3579, Z3580, Z5853, Z5854, Z5855, Z6021, Z6044, Z6045, Z6096, Z6097, Z6098,
Z6100, Z6102, Z6112, Z6142, Z6550, Z16492, Z16498, Z17857, Z17858, Z17859
• • • • •
• • • • •
• •
G2a2b2a1c1a1* -
• • • • •
• • • • •
• •
G2a2b2a1c1a1a Y88/Z3520
• • • • •
• • • • •
• • •
G2a2b2a1c1a1a* -
• • • • •
• • • • •
• • •
G2a2b2a1c1a1a1 FGC348,
FGC349
• • • • •
• • • • •
•
G2a2b2a1c1a2 Z3428, Z3292
• • • • •
• • • • •
• •
G2a2b2a1c1a2* -
• • • • •
• • • • •
• •
G2a2b2a1c1a2a Z6025, FGC7477/Z6523,
Z6024
• • • • •
• • • • •
• •
G2a2b2a1c1a2b Z3571, Z3572
• • • • •
• • • •
G2a2b2a1c2 FGC12126, FGC12121/Z16237,
FGC12129, FGC12130, FGC12135, FGC12138, FGC12145, FGC12152, FGC12156, FGC12159, FGC12175, Z16667
• • • • •
• • • • •
G2a2b2a1c2* -
• • • • •
• • • • •
G2a2b2a1c2a L660, L662
• • • • •
• • • • •
G2a2b2a1c2b Z16670
• • • • •
• •
G2a2b2a2 L694
• • • • •
• •
G2a2b2a3 M278
• • • • •
•
G2a2b2b PF3359,
CTS5434/PF3392, F705/PF3348, F795/PF3354, F1006/PF3260, F1175, F1429/PF3365,
F1581/PF3367, F1629/PF3368, F1760/PF3377, F2037,
F2419/PF3400, F3041/PF3414, PF3321, PF3404, PF3418,
F3425/PF3431, PF3432, FGC7257, FGC7260, PF3326, PF3375,
PF3388, PF3395, PF3396, PF3413, PF3417, Z6171, Z12223
• • • • •
• •
G2a2b2b* -
• • • • •
• •
G2a2b2b1 F1193/PF3362, F1705/PF3322, PF3430
• • • • •
• • •
G2a2b2b1* -
• • • • •
• • •
G2a2b2b1a F872/PF3355, F935/PF3356,
F1079, F1338, F1671, F1932/PF3383,
F2020, F2291/Z6442, F2537/PF3402, F3282, PF3369, PF3394, PF3401, PF3419, PF3434.2
• • • • •
• • •
G2a2b2b1a* -
• • • • •
• • • •
G2a2b2b1a1 PF3378, PF2829, PF3252, PF3349,
PF3358, PF3379, PF3385,PF3386, PF3390, PF3391, PF3393, PF3398,
PF3405, PF3412,PF3423, PF3433
• •
G2b M3115, M3145, M3191, PF1343, PF5721.2
Z8015, Z8016, Z8017, Z8018, Z8019,
Z8020, Z8021
• • •
G2b* -
• • •
G2b1 M377, L72/S315, L183
• • • •
G2b1* -
• • • •
G2b1a M283
An Extended Version of G Tree with STR Marker Categories
created by Content Expert Ray Banks.
Private SNPs - After having been investigated, these SNPs have not met the population distribution criteria for placement on the tree. Either too few confirmed positive testers have been found OR multiple confirmed testers were confined to either a single surname or to a small group of related males.
SNPs under Investigation - Additional testing is needed to confirm adequate positive samples and/or correct placement on the tree.
NOTES:
Y-DNA haplogroup G. Scholars have proposed dates ranging from 10,000 to 23,000 years
ago for the origin of this group using STR marker differences as the basis of their calculations. (Cinnioglu,
Genographic Project site, Semino). Counting the differences in numbers of SNP mutations, one study (Wei) suggested
that haplogroups more recent than haplogroup F (including G) had "a rapid expansion" dated at 41,000-52,000
years ago. Another study showed that haplogroup G was the first branching from haplogroup F among haplogroups G to T
(Poznik). And this latter study — again counting SNP mutations — calculated about the same time frame for
the emergence of haplogroup G based on its proportional branch length within its figure 2 which calculated the common
male ancestor of all living men as living 120,000 to 156,000 years ago. A final study (Francalacci) which calibrated
its calculations according to the first settlement of Sardinia gave an estimated age for haplogroup G as a separate
branch as 76,670 years (mean number of mutations of 374 multiplied by 205 years per mutation, according to their data).
Researchers have also suggested various places in western Asia as the site of origin of G, but the lack of ancient
DNA from that period makes confirmation of this difficult. Aunitary concept of haplogroup G often has little practical
importance because virtually all G men belong to G subgroups that arose much more recently and have differing
geographical distributions.
These are the most common G subgroups:
G1-M285 is a much less common form of G found in populations than is G2. All haplogroup G1
men so far have the 12 value at marker DYS392 — rarely seen in G except in G1 men (G project data). G1 reaches
parity with G2 only in parts of Iran reaching there up to 5 percent of all men. G1 is far less common in Europe,
North Africa and Asia (G Project data, Cinnioglu, Regueiro, and DYS392=12 G1 estimates from Adams, El-Sabai, Ferri,
Ghiani, Heber, Lovrecic, Nasidze-YHRD data from 3 studies, Rodriguez, Sengupta, Zalloua-2 studies). A Kazakh, a Middle
Eastern and two Ashkenazi Jewish G1 subgroups exist (Biro, G project data). Using STR marker differences, Rootsi
calculated the expansion time of M285 as 19,271 years ± 6,158 years.
G2a1-L293. All G2a1 (L293) men so far have the 10 value at marker DYS392 — rarely
seen in G except in L293 men. The subgroup P16 is found in high percentages in the central Caucasus Mountains area and
is rare elsewhere. Small clusters are found among Ashkenazi Jews, some eastern Europeans and among Maronite Christians
in Lebanon (Nasidze data in YHRD database, G project, Haber, Balanovsky and data). The Rootsi study — using STR
marker differences — calculated the coalescence age estimate for P16 at 9,400 years ago.
G2a2a-PF3146 men are found scattered throughout southwest and southern Asia and, though rare
in Europe, reach observable levels in Corsica and Sardinia (Keller, Francalacci, G Project data). A double value for
DYS19 in G is found almost exclusively within G2a2a though men with the same double value will not be reported as such.
G2a2a includes Oetzi, the Iceman mummy preserved for over 5000 years in the Italian Alps (Keller).
G2a2b1-M406 occurs in highest frequency in the eastern Mediterranean area reaching up to 5
percent of all men. A high percentage of M406 men have a value of 21 at marker DYS390 which is rare in G otherwise.
M406 is more common in southern Europe than in northern Europe. A distinctive Ashkenazi Jewish subgroup of M406
exists (King, Rootsi, G project and Cinnioglu data). One study using STR marker differences calculated the expansion
time for M406 in Anatolia at 12,800 years ago (Rootsi).
G2a2b2a1-L140 is the dominant G group in Europe (perhaps 80 percent of G samples) and may reach
up to about 7 percent of all men in a country but averages about 3 percent. A high percentage of G2a2b2a1 samples
form three major subgroups, Z725+ (DYS388=13 and predominantly CTS4803+), Z2022+ (YCA=20,21) and Z1903+ (DYS568=9).
One U1 subgroup within L140 (L1266) is the only L140 subgroup confirmed in some frequency outside Europe and that
only in the Caucasus region, particularly in the northwest (G Project, Balanovsky, Rootsi data). North of the
European borders of the once Roman Empire, the prevalence of these three L140 subgroups (and G in general) drops
considerably, and the three subgroups are found in noticeable amounts in almost all regions of the once Roman Empire
in Europe except among the Basques of Spain. An Ashkenazi Jewish cluster from northeastern Europe comprises about
half of the Z1903 subgroup, and this Jewish subgroup represents an exception to usual European boundaries mentioned.
An unusual concentration of Z1903 men occurs in Sardinia, and a high concentration of L497 was also found in isolated
valleys of southwestern Austria. The connection of the three main L140 subgroups to Sea Peoples, Etruscans, Alans
and Sarmatians and other groups who migrated to Europe is widely debated. Using differences in STR marker value
differences, Rootsi calculated the expansion time of the Z2022 subgroup as 7,100 years ± 2,300 years and 10,870
years ± 3,029 years for L497 in central Europe (All info from Berger, miscellaneous L140 data from Adams, Rootsi,
Francalacci and over 2,000 L140 samples in G project).
G2a2b2b1-CTS5434/PF3392 is found in noticeable numbers so far only in Sardinia (Francalacci
data).
G2b1-M377. Available M377 samples are either (a) those from Ashkenazi Jewish men from northeast
Europe who have a null value for marker DYS425 or (b) a small number of men from the Mediterranean areas and Armenia,
and more noticeably from Afghanistan, Pakistan and among Indian Pathans (Sengupta and G Project data). Using STR
marker differences Rootsi calculated a coalescence estimate of 5,600 years ago for M377 men, though the age of the
M377 is certainly much older.
References:
Adams et al,
The
Genetic Legacy of Religious Diversity and Intolerance: Paternal Lineages of
Christians, Jews, and Muslims in the Iberian Peninsula, American Journal of
Human Genetics, 83(6): 725-36, 2008.
Alonso et al,
The Place of the Basques in the European
Y-chromosome Diversity Landscape. (available by subscription) European Journal of
Human Genetics, 13:1293-1302, 2005.
Athey et al,
Y-SNP rs34134567 Defines a Large Subgroup of Haplogroup G2a-P15. (pdf)
Journal of Genetic Genealogy, 4(2):149-150, 2008.
Balanovsky et al,
Parallel Evolution of Genes and Languages in the Caucasus Region.
Molecular Biology and Evolution, 13 May 2011.
Behar et al,
Contrasting Patterns of Y Chromosome Variation in Ashkenazi Jewish and Host
Non-Jewish European Populations. (pdf) Hum Genet 114:354-365, 2004.
Behar et al,
Genome-Wide Structure of the Jewish People.
Nature, 446:238-42, 2010.
Berger et al,
High Resolution Mapping of Y haplogroup G in Tyrol (Austria).
Forensic Science International: Genetics, 7(5), 529-36, 2013.
Bertoncini et al,
The Dual Origin of Tati-speakers from Dagestan as Written in the Genealogy of Uniparental Variants.
(abstract) American Journal of Human Biology, Volume 24, Issue 4, pages 391-399, July/August 2012.
Biro et al,
A
Y-Chromosomal Comparison of the Madjars (Kazakhstan) and the Magyars
(Hungary),
American Journal of Physical Anthropology, 139(3): 305-10, 2009. (abstract)
Bosch et al,
Paternal and Maternal Lineages in the Balkans Show a Homogeneous Landscape over Linguistis Barriers
except for the Isolated Aromuns.
Annals of Human Genetics, 70:459-87, (2006).
Cinnioglu et al,
Excavating Y-chromosome Haplotype Strata in Anatolia. (pdf) Human Genetics. 114:127-148, 2004.
Cruciani et al,
A Back Migration from Asia to Sub-Saharan Africa Is Supported
by High-Resolution Analysis of Human Y-Chromosome Haplotypes.
American Journal of Human Genetics, 70:1197-1214, 2002.
El Sibai et al,
Geographical
Structure of the Y-Chromosomal Genetic Landscape of the Levant: A Coastal Inland
Contrast, Annals of Human Genetics, 73:568-81, 2009. (abstract)
Francalacci et al,
Low-Pass DNA Sequencing of 1200 Sardinians Reconstructs European Y-Chromosome Phylogeny.
Science: Vol. 341 no. 6145, pp. 565-569, DOI: 10.1126/science.1237947, 2 August 2013.
Ghiani et al,
Population data for Y-chromosome haplotypes defined by AmpFlSTR YFiler PCR amplification kit in
North Sardinia (Italy), Collegium Antropologicum, 33 (2): 643-51, 2009.
Haber et al,
Influences
of History, Geography, and Religion on Genetic Structure: the Maronites in
Lebanon, European Journal of Human Genetics, 19(3): 334-40, 2010.
Herrera et al,
Neolithic Patrilineal Signals Indicate that the Armenian Plateau was Repopulated by Agriculturalists.
European Journal of Human Genetics, 10.1038/ejhg.2011.192, 2011.
Karafet et al,
New Binary Polymorphisms Reshape and Increase Resolution of the Human Y-Chromosomal Haplogroup
Tree. Abstract. Genome Research, published online April 2, 2008.
Supplementary Material.
Keller et al,
New Insights into the Tyrolean Iceman's Origin and Phenotype as Inferred by Whole-genome Sequencing.
Nature Communications, DOI: 10.1038/ncomms1701, 2023.
King et al,
The
Coming of the Greeks to Provence and Corsica: Y-Chromosome Models of Archaic
Greek Colonization of the Western Mediterranean, BMC Evolutionary Biology, 11: 69, 2011.
King et al,
Differential Y-chromosome Anatolian Influences on the Greek and Cretan Neolithic., Annals of
Human Genetics, 72:205-214, 2008.
Kivisild et al,
The Genetic Heritage of the Earliest Settlers Persists in Both Indian Tribal and Caste
Populations. (pdf) American Journal of Human Genetics, 72: 313-332, 2003.
Nasidze et al,
Genetic Evidence Concerning the Origins of the South and North Ossetians. (pdf)
Annals of Human Genetics, 68: 588-599, 2004.
Nasidze et al,
MtDNA and Y-chromosome Variation in Kurdish Groups. (abstract) Annals of Human Genetics,
69: 401-412, 2005.
Nasidze et al,
Testing
Hypotheses of Language Replacement in the Caucasus: Evidence from the
Y-chromosome, Human Genetics 112 (3): 255-61, 2003.
Olalde et al,
Genomic Analysis of the Blood Attributed to Louis XVI (1754–1793), King of France.,
Scientific Reports, 4, Article number: 4666, doi:10.1038/srep04666, 2014.
Poznik et al,
Sequencing Y Chromosomes Resolves Discrepancy in Time to Common Ancestor of Males Versus Females. (abstract)
Science, 341 (6145): 562-5. 2013.
Regueiro et al,
Iran: Tricontinental Nexus for Y-Chromosome Driven Migration. (abstract)
Human Heredity, Vol. 61, No 3, 132-143, 2006.
Rootsi et al,
Distinguishing the Co-Ancestries of Haplogroup G Y-Chromosomes in the Populations of Europe and the Caucasus.
Abstract. European Journal of Human Genetics, (e-pub 16 May 2012 ahead of print), pp 1-8.
Semino et al,
Ethiopians and Khoisan Share the Deepest Clades of the Human Y-Chromosome Phylogeny. (pdf)
American Journal of Human Genetics, 70: 265-268, 2002.
Sengupta et al,
Polarity and Temporality of High Resolution Y-chromosome Distributions in India
Identify Both Indigenous and Exogenous Expansions and Reveal Minor Genetic Influence
of Central Asian Pastoralists. (pdf)
American Journal of Human Genetics, 78: 202-221, 2006.
Shen et al, Reconstruction
of Patrilineages and Matrilineages of Samaritans and other Israeli Populations from Y-Chromosome
and Mitochondrial DNA Sequence Variation. (pdf) Human Mutation, 24: 248-260, 2004.
Sims L M, Garvey D, Ballantyne J (2006).
Differentiation of sub-populations within Y-SNP haplogroup G, (poster citation - not available online)
Forensic Science Society, Autumn Conference, Wyboston, UK, November 3-5, 2006.
Sims L M, Garvey D, Ballantyne J (2009).
Improved Resolution Haplogroup G Phylogeny in the Y Chromosome, Revealed by a Set of Newly Characterized SNPs. (pdf)
PLoS One, 4: 6, e5792, 2009.
Valone et al,
Y SNP Typing of African-American and Caucasian Samples Using Allele-Specific
Hybridization and Primer Extension. (pdf) Journal of Forensic Science, 49: 4, July 2004.
Wei et al,
A Calibrated Human Y-Chromosomal Phylogeny Based on Resequencing.
Genome Research, 23(2): 388-95, 2013.
Zalloua et al,
Identifying
Genetic Traces of Historic Expansions: Phoenician Footprints in the
Mediterranean, American Journal of Human Genetics, 83: 633-42, 2008.
Zalloua et al,
Y Chromosome Diversity in Lebanon is Structured by Recent Historical Events. (abstract)
The American Journal of Human Genetics, Volume 82, Issue 4, 873-882, 28 March 2008.
Zhao et al,
Presence of Three Different Paternal Lineages among North Indians: A Study of 560 Y Chromosomes. (abstract)
Annals of Human Biology, 36(1): 46-59, 2009.
Additional Resources:
ISOGG Wiki - What you need to know about Genetic Genealogy.
Haplogroup G (Y-DNA) Project, Ray Banks,
Paul Givargidze, Rolf Langland, Whit Athey.
Haplogroup G Project, Ray Banks.
Haplogroup G2b-M377 / L72 / L183 / M283 Y Haplogroup Project (formerly G2c), Ted Kandell.
Corrections/Additions made since 1 January 2014:
Back to Main Page Back to Y-DNA Tree Trunk Back to SNP Index Back to Papers/Presentations Cited Back to Glossary Back to Listing Criteria Copyright 2014. International Society of Genetic Genealogy. All Rights Reserved. |