HIDE SNP NAMES

The Big Tree: R-A641

R-P312/S116 > Z40481 > ZZ11 > DF27/S250 > ZZ12 > ZZ19 > Z31644 > Z42772 > BY2285 > FGC22202 > A641

A641 FGC19598
FGC22210 Y7941
Y5058 FGC22195
Y5059 FGC22205
Y5060 FGC22211
Y5062 FGC22194
FGC22193
Y5063 FGC22196
Y5064 FGC22217
Y5066 FGC22207
FGC22218 Y7942
15255773-T-G
Y5067 FGC22212
Y5068 FGC22198
Y5069 FGC22206
Y5070 FGC22224
Y5077 FGC22203
21464195-A-AGAAG
Y5073 FGC22209
FGC22208
FGC22225 Y7940
22448972-G-T
Y7366 FGC22201
Y5061 FGC22192
Y5065 FGC22191
24729171-C-T
6523513-T-C
PH5187
M756 F3032
Y19623
Y19621
8315398-C-T
25934999-T-C
17893289-G-T
PF727
15536598-A-G
Z25950
PH5150
23591457-C-G
7092135-G-T
16585235-T-A
21433611-C-A
7776161-T-C
7401824-C-T
15080475-A-G
15810621-T-C
16822424-T-C
YP617
16986091-A-C
17494877-G-T
17530064-C-G
25029952-T-C
Butler
155150
Ryan
325245
Dwyer
N88747
Ryan
B8280
Smith
115560
Ryan
B79146
Ryan
349432
Ryan
B167367
Foley
79047
Parsons
489156
1k Genomes
HG01879
Grant
152505
Cahoo
169776
O'Dwyer
65918
Carroll
198624
Unknown
273017
Carew
305367
Cosgrove
B52811
Cosgrove
556125
Cosgrove
331268
Sheehy
B100083
Wilkinson
121153
Kennedy
59497 D8FCK
Condra
50661
Ryan
472126
Naughton
145027

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.