HIDE SNP NAMES

The Big Tree: R-Z37492

R-P312/S116 > Z40481 > ZZ11 > DF27/S250 > ZZ12 > ZZ19 > Z31644 > Z42772 > Z37492

Z37492 is a deletion GGTACAACAT->G at position 7235474. It doesn't show up in all BigY tests.
Z37492
PH2047
22230548-A-G
FGC49734
5606586-C-A
FGC49736
FGC49737
FGC49740
FGC49741
15106176-AAC-A
FGC49742
FGC49743
FGC49745
FGC49746
FGC49747
FGC49748
FGC49750
Z1513
FGC49755
FGC49756
FGC49757
FGC49758
24383769-C-CA
A7014
FGC49732
15460394-TAAGAG-T
BY3292
FGC49739
FGC49753
BY2278
FGC49744
FGC49751
22302389-A-C
FGC23535
FGC23545
FGC40704
BY18419
BY18420
BY18421
BY18422
BY18423
BY18424
BY18425
8819168-A-AT
BY18427
BY18428
BY18429
BY18430
BY18431
BY18432
BY18433
BY18434
FGC10577
BY18435
BY18436
BY18437
BY18438
BY18439
BY18440
BY18441
BY18442
BY18443
BY2039
BY18444
BY25224
BY18445
BY18446
BY18447
BY18448
BY18449
22467332-T-G
22467318-A-C
Z17105
BY18450
McReynolds
N50629
O'Neill
N103104
Williams
349715
O'Neill
139142
O'Neale
312665
Payne
55909
O'Neill
86442
O'Neill
36315
1k Genomes
NA12814
Frappat
E11281
Kidd
N4591 L6CA8
Picart
602820
Gleason
421690
Gleason
101333
Gleason
292050
Walker
98943
Turner
248573

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.