SHOW SNP NAMES

The Big Tree: R-CTS1751

R-P312/S116 > Z290 > L21/S145 > DF13 > Z39589 > CTS1751

14048611-A-G
14435863-G-GA
[ N/A ]
17937269-T-C
24661527-C-T
14484611-G-T
16640606-G-A
7274352-T-C
7356592-C-G
7356596-T-C
7653015-A-T
8265951-G-A
9854715-A-G
17757799-G-A
21402261-G-T
22144855-A-G
22445303-C-T
22460463-A-G
8101674-C-T
23150240-C-T
23191365-G-C
8059533-G-T
8140933-C-T
8503786-C-T
9850032-T-G
13200022-G-T
13852842-G-A
14838753-T-G
14847603-C-T
16717174-G-T
18646345-A-G
18752368-A-G
22157657-T-C
22242796-A-G
22711460-T-TA
23267677-C-A
22473901-T-A
15830211-GT-G
6096559-T-A
23473552-G-T
19401219-C-T
22312709-C-T
8358756-T-C
18849710-C-T
21834577-A-G
22458722-C-A
2669508-C-G
8523661-T-C
8611874-G-A
14583793-A-G
16744787-T-A
17196852-A-C
17887617-G-T
19439099-A-G
21253374-C-T
22568623-C-T
9422290-C-A
21294548-G-T
6817955-A-G
7159676-T-C
7291378-G-A
8538940-T-G
9393291-T-G
9417186-A-C
9574558-A-G
14198363-T-C
14248240-G-T
15258051-T-C
15266879-A-G
15754993-G-A
16578022-C-T
17014167-C-T
17593941-T-A
17604058-G-A
18045807-G-A
19008245-A-G
19407077-C-T
21906925-C-T
21961687-A-T
22466081-G-T
22478823-C-G
22487342-T-A
22722408-G-A
22921034-A-C
23636262-A-G
23761802-G-A
24767580-G-GT
25215716-A-C
16780260-C-T
23790512-A-T
10059575-G-A
Case
N82444
1k Genomes
NA12340
Fallin
211618 YF05985
Markham
315413
Phelan
55192
Whelan
83115 YF05111
Whalen
391645
MacMaster
107682
Brazile
187485
Brassil
168985
Prosser
57993
Capp
381772
Gadow
503185
Hogshead
434089
Horton
274385 YF06147
Horton
237130
Horton
478754
Redden
141799
Venn
380041

Overlay STR Data for an STR:


Oakes
H2290
Porter
N28007
Men whose NGS data have been fully analyzed are indicated with a grey background color. Red 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.

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.