HIDE SNP NAMES

The Big Tree: R-~22449881-G-T

R-P312/S116 > Z290 > L21/S145 > DF13 > Z39589 > Z251/S470 > FGC13899 > ~22449881-G-T

2017-06-20: This block contains the DYZ19 mutation 22449881-G-T, whose position is one of several possibilities. This mutation may in fact be upstream of the FGC SNPs positioned with it. Further testing is necessary.
22449881-G-T
FGC18233
25042060-A-G
FGC18235
FGC18240
FGC18230 Z37220
FGC18246
FGC18247
FGC18248
FGC18249
FGC18251
FGC18253
FGC18254
BY43344
FGC18256
FGC18258
FGC18259
FGC18260
FGC62375
FGC18265
FGC18268
FGC18269
FGC18271
FGC18272
FGC18274
FGC18276
BY24442
FGC18262
FGC18267
FGC18234
FGC18255
14708427-AAT-A
Y28752
BY51870
BY39094
BY39095
8677296-T-TC
BY39096
BY39097
BY39098
Y91373
BY39099
BY39100
BY39101
BY39102
BY39103
18953111-AT-A
BY39104
BY39105
BY39106
BY133903
BY39107
22440865-C-A
BY39109
BY39110
BY39111
BY2914
BY2920
BY2963
BY2964 BY23749
A7790 BY2973
A7791 BY2975
BY2982
FGC23554 Y6204
BY2983
BY2986
BY2995
BY24061
BY3003
BY3012
BY3014
BY3016
BY3034
BY3054
BY3067
BY3090
Godwin
139697 0ANEE
Godwin
728787
Renfroe
384581
Price
9452
Courtney
692859
Cole
283647
Law
48048
Stapleton
214154
Dorr
N112316
Castle
189806
1k Genomes
NA11831
Cook
297627 1588

Overlay STR Data for an STR:


Porter
N28007
Oakes
H2290
Williamson
196041
A red background is used for men whose data has not yet been fully analyzed. His position on the tree is not yet final, and will in general be downstream of the current position. He may not be positive for all the SNPs/INDELs in the block he descends from.

Men whose NGS data have been fully analyzed are indicated with a grey background color.

Those men with a grey background and a pink bar to their left have been finalized, but haven't gone through as much scrutinity as earlier kits have. In particular, no search has been made for recurrent SNPs or other unusual mutations. For the vast majority of kits, this has no effect at all, but I will review them as necessary in the future.

CTS4296
22233413-G-A
Mutations written with a red background fall within a region of the Y chromosome, such as the palindromic region, which has left the position of the mutation ambiguous. The true mutation may be at the indicated position, or at any one of a number of alternate positions.