HIDE SNP NAMES

The Big Tree: R-FGC14641

R-P312/S116 > Z40481 > ZZ11 > U152/S28 > L2/S139 > Z41150 > DF90 > FGC14641

FGC14641 Y12051
FGC29434
FGC29430
FGC29432
22237861-G-A
FGC29470
2687788-G-A
6620538-C-T
7845076-T-A
8309294-C-A
8656696-G-T
9125229-G-A
13819437-G-A
14372614-T-C
14707531-C-T
15878311-G-A
16649961-G-T
18076800-G-A
18160722-G-A
19212581-C-T
21070211-C-T
21183150-G-A
22263326-C-A
22444543-T-A
22834844-A-C
23326251-G-A
24507289-G-C
26725109-A-T
7725113-A-T
8406207-G-A
9450817-C-A
14977589-G-A
15955623-A-G
19103203-T-C
21478591-C-A
S18462
BY3512 FGC42922
BY3490 FGC42920
17651518-G-C
19291252-C-T
2877055-C-T
7152111-T-C
8491034-A-G
9809180-A-T
14084559-G-T
14906848-G-A
14928497-GCA-G
15223038-T-C
15459024-C-G
16508073-A-G
16607081-G-T
17310426-C-G
17841508-G-T
18103031-G-GT
Y7884 FGC28482
21343442-A-G
22245851-A-C
22294109-T-G
22463438-C-T
22571498-C-T
23492218-G-A
Chirstopher
450060 ZVU4C
Christopher
499042
Fry
B132018
Viau
N113299 744LV
Dinçer
321135
Hanni
171601
1k Genomes
HG02436
Toth
10698
Liston
305360
Alliston
499632
Copeland
421227
Hoppes
21225 W4ZLR

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.