SHOW SNP NAMES

The Big Tree: R-S1051

R-P312/S116 > Z290 > L21/S145 > DF13 > Z39589 > S1051

YSEQ Group 15: If you are R-S1051 and have tested with YSEQ, please join YSEQ Group 15.

There are a number of SNPs added to this block that only occur in the results of Moore (UTU7E, 357511) and the 1kG kit. These mutations are not covered by the BigY and additional testing will be necessary to determine where they belong.
16349104-C-T
16264788-T-A
13824242-G-T
21624482-C-T
19996272-C-T
24587965-T-C
6843890-G-A
6971284-G-T
7715204-G-A
13471255-C-A
14993243-C-A
16493545-T-C
16493555-C-T
16493556-A-C
16493560-C-A
16493635-G-A
18755559-T-C
21453288-C-T
22787897-G-A
15607324-G-T
22446018-G-C
22457392-G-C
24355850-A-G
6658322-A-C
7034708-T-C
8297646-A-T
8337146-G-A
8696622-G-T
13672629-G-T
13674855-C-A
14317730-T-A
15206583-G-C
15860028-G-A
15909961-T-C
15939413-T-C
16510976-C-G
17915815-G-T
18122992-T-C
18944442-C-T
18953247-A-G
19284264-G-C
19469783-G-T
21760907-T-C
22132156-G-C
24421272-C-T
24439146-G-A
16964767-A-G
16304008-C-A
4567341-C-A
8978087-G-A
15915724-C-T
16937513-G-T
16983358-C-T
17046051-TAG-T
17400634-C-T
17997132-A-T
22523835-T-A
21046495-A-G
21258195-G-C
21355595-A-G
21451640-C-T
22555380-A-AT
22870054-A-G
Hartley
306137
Brewer
303947
Hogge
99054
Ackley
B37138
Moore
357511 UTU7E
Dixon
326760
Smith
331890
Watkins
102970
Raburn
30949 5MZY9
Henry
316659
1k Genomes
HG01953
Tavares de Melo
476007
Cambray
497330
Porter
N8772
Wilson
220353
Britton
191679
Hammond
188927
McLellan
336065

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.