HIDE SNP NAMES

The Big Tree: R-CTS9490

R-P312/S116 > Z40481 > ZZ11 > U152/S28 > L2/S139 > Z41150 > Z49 > Z142/S211 > Z150 > CTS9490

CTS9490
CTS7970 S7404
FGC46210
Y20350 FGC46197
Y20351 FGC46198
CTS8125
Y20354 FGC46202
Y20418 FGC46213
22470616-T-G
Y20426 FGC46216
Y20420 FGC46192
Y20348 FGC46201
Y20421 FGC46208
Y20422 FGC46196
Y20349 FGC46200
15442163-ACC-A
Y20419 FGC46193
Y20423 FGC46204
Y20353 FGC46191
Y20355 FGC46194
FGC46203
BY33633
BY33634
Y20424 FGC46199
CTS11355
CTS11381
Y20357 FGC46195
23380162-TTATTTATTTATG-T
FGC46215
24220899-A-T
Y20425 FGC46207
BY33640
26594842-C-T
A8452
A8453 BY1438
A8454 S7409
A8456
24432437-T-TA
BY3624 A8812
Y17091 FGC37041
Y17094 FGC37043
Y17092 FGC37040
FGC37044
CTS2066
Y17093 FGC37045
Y17080 FGC37046
Y17082 FGC37047
Y17095 FGC37048
Y17084 FGC37049
Y17085 FGC37050
Y17096 FGC37051
Y17088 FGC37052
Y17076 FGC37053
Y17077 FGC37054
Y17078 FGC37055
Y17079 FGC37056
Y17081 FGC37057
Y17083 FGC37058
Y17086 FGC37059
Y17087 FGC37060
21928979-AAGAG-A
FGC37063
Y17089 FGC37064
Y17090 FGC37065
CTS10135 M7531
FGC37062
1k Genomes
HG00244
Tucker
111766
Harding
207883
Henderson
232800 YF01926
Graves
1620
Forrest
84690
Fay
203575
1k Genomes
NA20812
unknown
274660

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.