Tree Position

A0-T-YP2191 > P305[A1] > A1b > BT/A1b2 > M168/PF1416[CT] > P143[CF] > M89/PF2746[F] > F1329/M3658[GHI > F929[HIJK] > IJK > IJ > M170[I] > Z2881 > DF29 > Z58 > Z59 > Z62 > Z60 > Z140 > 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 STRBigY3
282347
hg38:Y:56834583-C-T A*
hg19:Y:13449360-C-T hg38:Y:11293684-C-T A*
hg38:Y:56835435-C-A A*
hg19:Y:18374799-G-A hg38:Y:16262919-G-A P6_Prx A*
hg19:Y:19888043-A-AT hg38:Y:17776163-A-AT P5_Prx A*
hg19:Y:24256803-A-G hg38:Y:22110656-A-G P3_b1 A*
hg19:Y:24298241-G-C hg38:Y:22152094-G-C P3_t1 A*
hg19:Y:24302675-A-C hg38:Y:22156528-A-C P3_t1 A*
hg19:Y:25940809-C-T hg38:Y:23794662-C-T P1_Y1 A*
hg19:Y:28816512-T-A hg38:Y:26670365-T-A A*
hg19:Y:28817492-T-G hg38:Y:26671345-T-G A*
hg38:Y:56831746-T-A A*
hg38:Y:56835649-A-T A*
hg38:Y:56837970-G-C A*
hg19:Y:13820614-C-T hg38:Y:11699908-C-T BY51113 DYZ17 +
hg38:Y:10865498-A-G FT434653 +
hg19:Y:13845295-G-T hg38:Y:11724589-G-T FT328688 DYZ17 +
hg19:Y:8341966-G-A hg38:Y:8473925-G-A YY+
hg19:Y:9092220-G-A hg38:Y:9254611-G-A FT61276 Y+
hg19:Y:13852475-C-T hg38:Y:11731769-C-T BY199299 DYZ17 +
hg19:Y:2658357-G-C hg38:Y:2790316-G-C FT280243 YY+
hg19:Y:2785190-T-G hg38:Y:2917149-T-G FT275642 YY+
hg19:Y:3111526-G-A hg38:Y:3243485-G-A FT275709 +
hg19:Y:3980045-A-G hg38:Y:4112004-A-G FT275877 +
hg19:Y:5460683-G-T hg38:Y:5592642-G-T FT276181 +
hg19:Y:6728252-G-A hg38:Y:6860211-G-A FT276377 Y+
hg19:Y:7567988-C-T hg38:Y:7699947-C-T YY+
hg19:Y:8012985-G-A hg38:Y:8144944-G-A YY+
hg19:Y:8152103-T-G hg38:Y:8284062-T-G FT276604 YY+
hg19:Y:8204242-G-A hg38:Y:8336201-G-A YY+
hg19:Y:8283632-G-C hg38:Y:8415591-G-C FT276627 YY+
hg19:Y:8886775-A-C hg38:Y:9018734-A-C FT276748 Y+
hg19:Y:9075029-A-T hg38:Y:9237420-A-T BY11996 Y+
hg19:Y:9980140-G-A hg38:Y:10142531-G-A FT373685 Y+
hg19:Y:13681227-A-G hg38:Y:11525551-A-G FT448219 DYZ17 +
hg19:Y:15382548-T-C hg38:Y:13270668-T-C FT277186 YY+
hg19:Y:15497365-A-C hg38:Y:13385485-A-C FT277206 YY+
hg19:Y:15758283-G-C hg38:Y:13646403-G-C FT277269 YY+
hg19:Y:16838131-G-GAT hg38:Y:14726251-G-GAT +
hg19:Y:17875586-A-C hg38:Y:15763706-A-C FT277677 YY+
hg19:Y:18129027-C-T hg38:Y:16017147-C-T FT277729 YY+
hg19:Y:18771801-A-G hg38:Y:16659921-A-G YY+
hg19:Y:20831954-G-A hg38:Y:18670068-G-A FT283930 P4_Gap +
hg19:Y:22069534-GTTTAA-G hg38:Y:19907648-GTTTAA-G +
hg19:Y:22516005-A-G hg38:Y:20354119-A-G FT278212 Y+
hg19:Y:22832383-A-G hg38:Y:20670497-A-G FT278282 YY+
hg19:Y:13669483-GATGGAATGGAATGGA-G hg38:Y:11513807-GATGGAATGGAATGGA-G DYZ17 10×ATGGA*
hg19:Y:8513023-C-T hg38:Y:8644982-C-T YY*
hg19:Y:20104255-G-A hg38:Y:17992375-G-A P5_Dst *
hg19:Y:22512889-G-A hg38:Y:20351003-G-A L627BY12307 DYZ19 **
hg19:Y:21787578-A-G hg38:Y:19625692-A-G **
hg38:Y:10629652-C-A **
hg19:Y:8690208-ATTTT-A hg38:Y:8822167-ATTTT-A 29×T**
hg38:Y:10629638-A-T **
hg19:Y:15412990-T-C hg38:Y:13301110-T-C **
hg38:Y:10629664-T-G **
hg19:Y:3949394-G-A hg38:Y:4081353-G-A **
hg19:Y:5457703-T-C hg38:Y:5589662-T-C **
hg19:Y:14488293-G-A hg38:Y:12367562-G-A **
hg19:Y:21527746-C-T hg38:Y:19365860-C-T **
hg19:Y:22280439-A-T hg38:Y:20118553-A-T DYZ19 **
hg19:Y:22623176-C-T hg38:Y:20461290-C-T **
hg19:Y:22778778-G-A hg38:Y:20616892-G-A **
hg19:Y:21923295-AT-A,ATT hg38:Y:19761409-AT-A,ATT 15×T***
hg19:Y:13461068-A-G hg38:Y:11305392-A-G ***
hg19:Y:23421043-ATTTTT-A hg38:Y:21259157-ATTTTT-A 22×T***
hg19:Y:20842517-GGAAA-G,GGAAAGAAA hg38:Y:18680631-GGAAA-G,GGAAAGAAA P4_Dst 14×GAAA***
hg19:Y:7363157-TAAA-T hg38:Y:7495116-TAAA-T 18×A***
hg19:Y:28724174-A-ATTT hg38:Y:26578027-A-ATTT 20×T***
hg19:Y:21827606-CAAAAA-C hg38:Y:19665720-CAAAAA-C 21×A***
hg19:Y:7269610-CTT-C,CTTT hg38:Y:7401569-CTT-C,CTTT 22×T***
hg19:Y:24242331-CAA-C hg38:Y:22096184-CAA-C P3_b1 16×A***
hg19:Y:3220600-G-GTT hg38:Y:3352559-G-GTT 14×T***
hg19:Y:21873566-CA-C,CAA hg38:Y:19711680-CA-C,CAA 14×A***
hg19:Y:13217240-CT-C,CTT hg38:Y:11061564-CT-C,CTT 16×T***
hg19:Y:14377480-T-C hg38:Y:12256776-T-C ***
hg19:Y:3630261-TC-T hg38:Y:3762220-TC-T ***
hg19:Y:3991460-C-T hg38:Y:4123419-C-T ***
hg19:Y:4880972-G-C hg38:Y:5012931-G-C ***
hg19:Y:5390045-G-T hg38:Y:5522004-G-T ***
hg19:Y:5865609-T-C hg38:Y:5997568-T-C ***
hg19:Y:6513774-G-A hg38:Y:6645733-G-A ***
hg19:Y:7723926-A-G hg38:Y:7855885-A-G ***
hg19:Y:13340795-T-C hg38:Y:11185119-T-C ***
hg19:Y:13474674-T-C hg38:Y:11318998-T-C ***
hg19:Y:22509134-C-T hg38:Y:20347248-C-T DYZ19 ***
hg38:Y:56835638-CA-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.

Age Analysis Information (work in progress)

AllMcDonaldYFull
Kit: 2823471475810192989318245673
Used in age calculations1475810192989318245673
Counts of SNPs1919
Variant counts last updated 2025-11-08 02:59:02.



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