Tree Position

Exact position not yet finalized.

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.

Position Blocks Names Region McDonald BED combBED STR1kG
HG02721
hg19:Y:14198294-C-T hg38:Y:12077588-C-T CTS212CTS2144 YY+
hg19:Y:18770243-C-A hg38:Y:16658363-C-A YY+
hg19:Y:9377326-T-G hg38:Y:9539717-T-G FGC7103 Y4005 Y+
hg19:Y:2984600-C-T hg38:Y:3116559-C-T +
hg19:Y:3936229-C-T hg38:Y:4068188-C-T FT132610 +
hg19:Y:4071270-A-T hg38:Y:4203229-A-T +
hg19:Y:4150838-C-T hg38:Y:4282797-C-T +
hg19:Y:4307065-T-A hg38:Y:4439024-T-A +
hg19:Y:4375278-G-A hg38:Y:4507237-G-A FT275976 +
hg19:Y:4687031-T-A hg38:Y:4818990-T-A FT276032 +
hg19:Y:4734349-G-A hg38:Y:4866308-G-A FT276041 +
hg19:Y:5726924-A-G hg38:Y:5858883-A-G FT276229 +
hg19:Y:6464472-T-C hg38:Y:6596431-T-C +
hg19:Y:6473776-G-A hg38:Y:6605735-G-A +
hg19:Y:7018731-A-T hg38:Y:7150690-A-T FT333647 Y+
hg19:Y:7018732-C-T hg38:Y:7150691-C-T FT333648 Y+
hg19:Y:7097887-C-A hg38:Y:7229846-C-A FT333692 Y+
hg19:Y:7219687-C-G hg38:Y:7351646-C-G Z37017 YY+
hg19:Y:7256280-A-T hg38:Y:7388239-A-T Z37018 Y+
hg19:Y:7308591-G-A hg38:Y:7440550-G-A Z37019 YY+
hg19:Y:7370306-T-C hg38:Y:7502265-T-C FT333840 Y+
hg19:Y:7395840-G-A hg38:Y:7527799-G-A M3940 YY+
hg19:Y:7830907-A-G hg38:Y:7962866-A-G Y30958 YY+
hg19:Y:9381293-G-A hg38:Y:9543684-G-A Y31788 Y+
hg19:Y:9909963-A-G hg38:Y:10072354-A-G Y+
hg19:Y:9927800-G-A hg38:Y:10090191-G-A Y+
hg19:Y:10029918-C-T hg38:Y:10192309-C-T Y+
hg19:Y:10072726-A-T hg38:Y:10235117-A-T FT427290 +
hg19:Y:13494731-A-C hg38:Y:11339055-A-C +
hg19:Y:13509558-G-A hg38:Y:11353882-G-A +
hg19:Y:13512549-C-A hg38:Y:11356873-C-A +
hg19:Y:13518431-A-G hg38:Y:11362755-A-G +
hg19:Y:13610818-A-T hg38:Y:11455142-A-T +
hg19:Y:13696621-A-G hg38:Y:11540945-A-G DYZ17 +
hg19:Y:13705878-G-A hg38:Y:11550202-G-A DYZ17 +
hg19:Y:13716627-T-A hg38:Y:11560951-T-A DYZ17 +
hg19:Y:13818562-C-T hg38:Y:11697856-C-T Y31784 DYZ17 +
hg19:Y:13842977-A-T hg38:Y:11722271-A-T Y31785 DYZ17 +
hg19:Y:13851485-T-C hg38:Y:11730779-T-C DYZ17 +
hg19:Y:13956972-C-T hg38:Y:11836266-C-T FT335151 Y+
hg19:Y:14246232-C-G hg38:Y:12125526-C-G FT335391 YY+
hg19:Y:14376515-G-C hg38:Y:12255811-G-C Y31789 YY+
hg19:Y:14530709-G-A hg38:Y:12418910-G-A FT13047 Y+
hg19:Y:14627990-C-T hg38:Y:12516058-C-T Y31783 YY+
hg19:Y:14641838-C-T hg38:Y:12529907-C-T Y31778 YY+
hg19:Y:14651816-G-A hg38:Y:12539881-G-A Y30960 YY+
hg19:Y:15372502-A-T hg38:Y:13260622-A-T FT336104 YY+
hg19:Y:15697354-T-G hg38:Y:13585474-T-G Y31786 YY+
hg19:Y:15723925-A-G hg38:Y:13612045-A-G FT336330 YY+
hg19:Y:15873476-C-A hg38:Y:13761596-C-A FT336447 YY+
hg19:Y:16092486-T-C hg38:Y:13980606-T-C FT336592 Y+
hg19:Y:16250489-T-C hg38:Y:14138609-T-C YY+
hg19:Y:16415256-A-G hg38:Y:14303376-A-G FT336764 YY+
hg19:Y:16461589-G-A hg38:Y:14349709-G-A FT336815 YY+
hg19:Y:16723739-C-T hg38:Y:14611859-C-T FT277454 Y+
hg19:Y:17206301-C-T hg38:Y:15094421-C-T FT337267 YY+
hg19:Y:17263762-C-A hg38:Y:15151882-C-A Y30961 YY+
hg19:Y:17525225-G-T hg38:Y:15413345-G-T FT337497 YY+
hg19:Y:17650757-G-C hg38:Y:15538877-G-C Y31787 YY+
hg19:Y:17738283-T-G hg38:Y:15626403-T-G FT337638 YY+
hg19:Y:18747009-G-T hg38:Y:16635129-G-T FT338221 YY+
hg19:Y:18776427-C-T hg38:Y:16664547-C-T Y9157 BY277 YY+
hg19:Y:18968164-G-C hg38:Y:16856284-G-C Y+
hg19:Y:19212176-A-C hg38:Y:17100296-A-C FT338563 YY+
hg19:Y:19357667-T-G hg38:Y:17245787-T-G BY128441 YY+
hg19:Y:20825088-C-T hg38:Y:18663202-C-T FT348165 P4_Gap +
hg19:Y:21079438-A-G hg38:Y:18917552-A-G FT338870 YY+
hg19:Y:21130219-G-C hg38:Y:18968333-G-C FT338909 YY+
hg19:Y:21444843-A-C hg38:Y:19282957-A-C Y30962 YY+
hg19:Y:21582542-C-T hg38:Y:19420656-C-T Y+
hg19:Y:21679317-C-A hg38:Y:19517431-C-A FT278095 Y+
hg19:Y:21701276-G-A hg38:Y:19539390-G-A FT339330 YY+
hg19:Y:22215735-C-T hg38:Y:20053849-C-T FT339694 Y+
hg19:Y:22469735-G-A hg38:Y:20307849-G-A FT278560 DYZ19 +
hg19:Y:22507414-G-A hg38:Y:20345528-G-A Y31779 DYZ19 +
hg19:Y:22780420-G-T hg38:Y:20618534-G-T Y+
hg19:Y:22842691-C-T hg38:Y:20680805-C-T Y31782 YY+
hg19:Y:22902946-G-T hg38:Y:20741060-G-T FT339960 YY+
hg19:Y:23004657-A-G hg38:Y:20842771-A-G FT340024 Y+
hg19:Y:23062307-G-A hg38:Y:20900421-G-A FT340073 Y+
hg19:Y:23134201-T-A hg38:Y:20972315-T-A FT340140 YY+
hg19:Y:23134202-G-T hg38:Y:20972316-G-T FT340141 YY+
hg19:Y:23556468-A-G hg38:Y:21394582-A-G FT340400 YY+
hg19:Y:24001174-G-A hg38:Y:21855027-G-A Y31780 Y+
hg19:Y:24373335-C-T hg38:Y:22227188-C-T Y+

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.




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