Tree Position

A0-T-YP2191 > P305[A1] > A1b > BT/A1b2 > M168/PF1416[CT] > M145/P205/PF144 > M96/PF1823 > M75

Unique Mutations

The mutations unique to this man are summarized in the table below. Those with a '+' or '*' confidence level are considered by FamilyTreeDNA or FullGenomesCorp to be high quality SNPs/INDELs. For completeness, all other mutations of lesser confidence are included as well. These additional mutations may be useful for distinguishing between very closely related men.

Occasionally, some of the mutations listed here will be thought to be shared with other men in which case they might appear in upstream blocks on the tree. When this happens, the 'Blocks' field will indicate what block they appear in. Such a situation might arise with BigY men if the BED data suggests another man may be positive for a SNP, even though it doesn't appear in his VCF data. It might also happen if Chromo2 testing or Sanger sequencing of other men not on the tree show the SNP to be shared.

POS-REF-ALT (hg19) POS-REF-ALT (hg38) Blocks Names Region McDonald BED combBED STR1kG
HG02771
17111749-C-T 14999869-C-T FGC8244 YY+
2736221-C-T 2868180-C-T FT315367 YY+
22478610-C-G 20316724-C-G DYZ19 +
2919998-C-A 3051957-C-A FT315437 +
3271194-T-C 3403153-T-C +
3463500-C-T 3595459-C-T FT317331 +
3671675-C-T 3803634-C-T FT318086 +
3937197-G-C 4069156-G-C FT318992 +
4138256-T-C 4270215-T-C FT319643 +
4165049-C-T 4297008-C-T FT88474 +
4460089-C-T 4592048-C-T FT320715 +
4903588-G-A 5035547-G-A FT322083 +
5103951-A-G 5235910-A-G FT322741 +
5126964-G-T 5258923-G-T FT322832 +
5193370-C-T 5325329-C-T +
6542607-G-C 6674566-G-C FT326866 +
6925834-T-C 7057793-T-C Z20784 YY+
7099946-T-C 7231905-T-C Z20785 YY+
7102222-G-T 7234181-G-T Z20786 Y+
7433733-T-C 7565692-T-C Z42545 Y+
7528407-C-A 7660366-C-A Z42546 YY+
8317156-T-C 8449115-T-C FT327508 YY+
8353684-C-G 8485643-C-G FT327518 YY+
8588133-C-T 8720092-C-T BY74298 YY+
9012809-C-T 9175200-C-T Y+
9965082-G-T 10127473-G-T Y+
10033733-G-A 10196124-G-A Y+
13364712-C-A 11209036-C-A +
13564116-A-G 11408440-A-G +
13605058-T-C 11449382-T-C +
13920881-T-G 11800175-T-G Y+
13964526-G-A 11843820-G-A FTA5908 Y+
14049534-G-T 11928828-G-T F18396 YY+
14209199-C-A 12088493-C-A FT329120 YY+
14267637-A-G 12146931-A-G FT329161 Y+
14331230-C-A 12210524-C-A FT329208 YY+
14923100-G-A 12811165-G-A YY+
15541626-A-C 13429746-A-C FTA5972 YY+
15767394-C-G 13655514-C-G BY103945 YY+
15805443-G-C 13693563-G-C FTA5976 Y+
15999808-G-A 13887928-G-A FT329825 YY+
16261711-C-T 14149831-C-T FT329899 YY+
16263670-G-A 14151790-G-A FT329900 YY+
16640329-C-T 14528449-C-T FT330049 YY+
17008727-G-T 14896847-G-T FT143966 YY+
17156457-G-C 15044577-G-C FT330278 YY+
17344319-T-C 15232439-T-C FT330359 YY+
17399933-T-C 15288053-T-C YY+
17413186-G-C 15301306-G-C FT330398 YY+
17424525-A-C 15312645-A-C FT330404 YY+
17634528-A-G 15522648-A-G FT330504 YY+
18026642-C-T 15914762-C-T FT330699 Y+
18122747-C-T 16010867-C-T FT330748 YY+
18160209-A-G 16048329-A-G FT330766 YY+
18179935-C-A 16068055-C-A FT330775 YY+
18186680-G-T 16074800-G-T FT330779 Y+
18383330-T-G 16271450-T-G FT330844 P6_Gap +
18539340-C-A 16427460-C-A FTA6104 Y+
18713754-G-C 16601874-G-C FT330974 YY+
18873815-G-A 16761935-G-A FT331057 Y+
18875328-G-C 16763448-G-C FT331060 Y+
19428208-A-C 17316328-A-C FT331311 Y+
20819553-C-T 18657667-C-T FT348155 P4_Gap +
21316399-A-C 19154513-A-C FT331501 YY+
21619683-A-G 19457797-A-G FT331672 YY+
21725480-T-C 19563594-T-C FT331707 YY+
21732294-C-A 19570408-C-A FT331710 YY+
21962495-A-G 19800609-A-G FT331824 YY+
21987510-G-A 19825624-G-A FT331838 YY+
22133969-T-C 19972083-T-C FT331900 YY+
22467000-G-T 20305114-G-T FT458742 DYZ19 +
22468446-G-T 20306560-G-T DYZ19 +
22483738-G-A 20321852-G-A FGC57843 DYZ19 +
23417702-T-A 21255816-T-A FT332337 YY+
23752063-C-T 21590177-C-T FTA6295 Y+
23794505-C-T 21632619-C-T Y+
23969528-G-A 21823381-G-A F26535 Y+
24398461-G-A 22252314-G-A FT332831 Y+
28491004-T-C 26344857-T-C +

In the table above, the meaning of the confidence field depends on whether the data comes from an FTDNA kit or an FGC kit. For FTDNA kits, + implies a "PASS" result with just one possible variant, * indicates a "PASS" but with multiple variants, ** indicates "REJECTED" with just a single variant, and *** indicates "REJECTED" with multiple possible variants. 'A*' are heterozygous variants not called by FTDNA, but still pulled from the VCF file. For FGC kits, + indicates over 99% likely genuine (95% for INDELs); * over 95% likely genuine (90% for INDELs); ** about 40% likely genuine; *** about 10% likely genuine. Manual entries read directly from a BAM file will be either + indicating positive, or * indicating that the data show a mixture of possible variants.

For the FTDNA kits, the BED data is encoded in the background color of the cells. Those cells with a white background have coverage, those with a grey background indicate no coverage in the BED file, and those with a pink background indicate the mutation is on the edge of a coverage region. These pink regions often indicate that the individual may be positive for a SNP even if there is no corresponding entry in the vcf file.

The combBED column indicates whether or not the mutation is a SNP and falls in the combBED region defined in Defining a New Rate Constant for Y-Chromosome SNPs based on Full Sequencing Data by Dmitry Adamov, Vladimir Guryanov, Sergey Karzhavin, Vladimir Tagankin, Vadim Urasin.

The McDonald BED column indicates whether or not the mutation is a SNP and falls in the BED region used by Dr. Iain McDonald in the age analysis he does for R-U106 men.