HIDE SNP NAMES

The Big Tree: R-27636437-G-A

R-P312/S116 > Z40481 > ZZ11 > DF27/S250 > ZZ12 > FGC20747 > FGC20764 > FGC20767 > FGC20770 > 27636437-G-A

BY27772
BY27771
FGC20749
FGC32547
FGC20750
FGC20751 V2240
FGC20752
FGC20754
FGC20756
FGC20761
FGC32550
Y19741
FGC20748
FGC20769
FGC32553
FGC20753
FGC20758
Y16482
FGC32548
FGC20759
FGC20760
FGC20762
FGC20763 V3476
FGC20766
21880252-AAT-A
27339768-A-C
ZZ12_1
FGC20765
BY27773
BY27774
FGC20755
BY27775
BY27776
BY27777
BY27778
A9700
BY27779
BY27780
FGC20816
FGC20821
FGC20819
A9510
BY27781
Y19740
A9509
A10500
BY27782
BY27783
Z16828
FGC20814
A10928
A10929
A10930
A10931
A10932
A10933
A10934
A10935
Y17780
Y17760
Y17783
Y17446
A10647
A10648
Y17763
Y17773
Y29071
Y28623
Y29072
BY22299
A11389
Y28624
PH2690
Y28625
Y29070
Y28626
Y29074
Y28629
A11390
Y28630
Y28631
Y29066
Y28632
Y29067
BY22300
Y29068
Y29069
Pikholz
201169
Spira
394364
Schapiro
76478
Finkelstein
B59863
Levy
F995L
Bachrach
268974
Reisch
133783
Moquist
552467
Royak
N93232
Persky
431305
Taubman
248611
Souroujon
191604
Esteves
253366
Fernandes
370301
Soares
458968
Ferrer
25139
Simoes
E2198
Melo
329413
Pool
91031
daSilva
B43396 YF09454

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.