HIDE SNP NAMES

The Big Tree: R-CTS10893

R-U106/S21 > Z381/S263 > Z301/S499 > L48 > Z9 > Z30/S271 > Z2 > Z7 > CTS10893

CTS10893 S3595
Y11028 FGC901
FGC903 S6909
Y10792 FGC914
Y3159 FGC924
17278346-GA-G
Y3158
CTS9241
Y11027 FGC930
Y3157 FGC935
FGC17839
FGC904 S6901
ZZ59
ZZ60
A8151
20036629-C-T
A9455
A9456
A10306
A9452
A9453
A10304
A10305
A9454
A9451
16969028-TTTACCATCAATCA-T
A10297
A10298
A10299
A10300
A10301
A10302
16863762-AC-A
A10303
17533611-CATTTACTAATTTAGTATTTTATTGT-C
18697332-A-C
18985273-C-A
19197629-G-T
19457180-A-T
20816615-T-G
21568796-G-A
21867305-T-C
23135087-C-T
1k Genomes
NA20586
Scott
260492
Reed
N18239
Jackson
48002
Scott
83016
Dettmann
94932
Pascoe
N92296
Nickel
N46232
Phipps
170781
Arnold
175373
Nail
351493
Firth
359279
Wooten
B2934
Moore
66143 FG1013A
Carr
267578 ESFPZ
Burrows
514501
Mortelliti
N25207
Cruff
135647
Mörtensson
117015
Wright
21555
Sweden
130856
Allen
N36644
Walls
N2035
Druecke
230496
Wright
236570
Svenonis
264754
Safsten
284006
Chaddock
345530
Smith
398477
Hansen
450672
Kjølstad
N92415
Wright
310422
Blackburn
402203
Woods
56993 UXCJ8
Fowler
169830 YF06355
Fowler
B10106
Anderson
522374
Burnett
277487
Davis
204451
Ozment
21791
Ozman
114801
Helmer
323561
Eadie
B3426

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.