HIDE SNP NAMES

The Big Tree: R-Z40483

R-P312/S116 > Z40481 > ZZ11 > U152/S28 > Z193 > Z40483

Z40483
CTS2617
Y16333
CTS4562
Y16335
3079273-C-T
CTS11993
FGC5033
FGC5034
FGC5049
FGC5053
FGC5055
FGC5058
FGC5061
FGC5063
FGC5065
FGC5029
FGC7975
FGC50736
FGC5023
FGC50737
FGC5025
FGC5026
FGC50738
FGC5028
FGC5030
FGC5031
FGC5032
FGC5035
FGC5036
FGC50740
BY3642
FGC5037
FGC5038
FGC5039
FGC5040
FGC5041
FGC5042
FGC5043
FGC5044
FGC5045
FGC5046
FGC5047
FGC5050
FGC5051
FGC5052
FGC5054
FGC5056
FGC5057
FGC5059
FGC5060
FGC5062
FGC5064
FGC50742
FGC50743
BY3627
BY3646
BY3851
BY3855
BY3856
BY3636
9700303-G-A
14328961-A-C
CTS7193
BY3647
BY3649
22239389-G-A
22489179-G-T
22489184-G-T
BY3860
FGC30121
2867356-TTTGGACCTTC-T
6778560-GC-G
8880669-C-A
8880741-G-C
FGC30128
FGC30130
FGC30133
FGC30140
FGC30144
9377005-T-G
9988214-G-C
BY3643
BY3847
BY3848
15485779-G-A
BY3854
17330600-C-T
17386454-G-C
S20550
FGC39876
Y6354
22273354-G-C
22463191-A-G
23300651-G-A
1k Genomes
NA20792
Perez
459604
Zafonte
N42592
Duncan
10814 ZG69A
Dunkin
253924 QTUWC
Boucher
285324
Fulfisk
N2620
Cantwell
160144
Presley
40733
Wear
133986
Hamilton
6716
Artis
373236
Andereggen
E7207

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.