Tree Position

A0-T-YP2191 > P305[A1] > A1b > BT/A1b2 > M168/PF1416[CT] > P143[CF] > M89/PF2746[F] > F1329/M3658[GHI > F929[HIJK] > IJK > K > M526[K2] > M2335 > F346[NO] > P191[O] > 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
NA18559
hg19:Y:28528051-C-T hg38:Y:26381904-C-T CTS12219 +
hg19:Y:17480036-A-G hg38:Y:15368156-A-G BY80068 L96CTS7435 YY+
hg19:Y:22016986-C-A hg38:Y:19855100-C-A Y+
hg19:Y:22657362-T-C hg38:Y:20495476-T-C FGC54555 YY+
hg19:Y:2922844-C-T hg38:Y:3054803-C-T +
hg19:Y:2989225-G-A hg38:Y:3121184-G-A +
hg19:Y:3242583-G-A hg38:Y:3374542-G-A +
hg19:Y:3647114-A-T hg38:Y:3779073-A-T +
hg19:Y:4573825-C-T hg38:Y:4705784-C-T +
hg19:Y:5446770-A-G hg38:Y:5578729-A-G +
hg19:Y:5770227-T-A hg38:Y:5902186-T-A +
hg19:Y:6046683-A-C hg38:Y:6178642-A-C +
hg19:Y:7034076-A-G hg38:Y:7166035-A-G Y31268 YY+
hg19:Y:7727999-C-T hg38:Y:7859958-C-T FT300233 YY+
hg19:Y:7946774-G-T hg38:Y:8078733-G-T F16467 YY+
hg19:Y:8203459-C-T hg38:Y:8335418-C-T BY58804BY70699 YY+
hg19:Y:8410824-T-G hg38:Y:8542783-T-G F17003 YY+
hg19:Y:8428069-C-T hg38:Y:8560028-C-T F1190 YY+
hg19:Y:8472073-A-G hg38:Y:8604032-A-G F1232 YY+
hg19:Y:8652899-T-G hg38:Y:8784858-T-G F17351 YY+
hg19:Y:9836764-C-T hg38:Y:9999155-C-T F1615 YY+
hg19:Y:10010871-G-A hg38:Y:10173262-G-A BY82872 Y+
hg19:Y:10075183-A-T hg38:Y:10237574-A-T +
hg19:Y:10080781-G-A hg38:Y:10243172-G-A +
hg19:Y:13218310-C-T hg38:Y:11062634-C-T F1657 +
hg19:Y:13311323-G-A hg38:Y:11155647-G-A BY85081 +
hg19:Y:13457034-T-C hg38:Y:11301358-T-C BY85477 +
hg19:Y:13459826-T-C hg38:Y:11304150-T-C BY85593 +
hg19:Y:13610984-C-T hg38:Y:11455308-C-T +
hg19:Y:13693028-T-C hg38:Y:11537352-T-C DYZ17 +
hg19:Y:13815692-C-T hg38:Y:11694986-C-T BY160162 DYZ17 +
hg19:Y:14007811-A-G hg38:Y:11887105-A-G F18330 YY+
hg19:Y:14138685-C-T hg38:Y:12017979-C-T F1701 YY+
hg19:Y:14289593-G-A hg38:Y:12168887-G-A CTS2395 YY+
hg19:Y:14393342-G-C hg38:Y:12272638-G-C Y32363 YY+
hg19:Y:14697942-A-G hg38:Y:12586008-A-G FT300990 YY+
hg19:Y:14793801-A-T hg38:Y:12681872-A-T CTS3280 Y+
hg19:Y:14957198-G-C hg38:Y:12845273-G-C F1874 YY+
hg19:Y:15153274-C-T hg38:Y:13041361-C-T CTS3753 YY+
hg19:Y:15417237-A-T hg38:Y:13305357-A-T F1946 YY+
hg19:Y:15471307-A-G hg38:Y:13359427-A-G F1954 YY+
hg19:Y:15890217-G-T hg38:Y:13778337-G-T Y+
hg19:Y:16508150-C-T hg38:Y:14396270-C-T CTS5852 YY+
hg19:Y:16601236-T-C hg38:Y:14489356-T-C YY+
hg19:Y:16613268-G-C hg38:Y:14501388-G-C YY+
hg19:Y:16782018-A-T hg38:Y:14670138-A-T F2263 YY+
hg19:Y:16801589-G-A hg38:Y:14689709-G-A FGC24706 YY+
hg19:Y:16861969-G-A hg38:Y:14750089-G-A F2302 YY+
hg19:Y:16998640-T-A hg38:Y:14886760-T-A FT301521 Y+
hg19:Y:17009212-A-G hg38:Y:14897332-A-G CTS6612 YY+
hg19:Y:17164889-G-T hg38:Y:15053009-G-T Y+
hg19:Y:17423042-T-A hg38:Y:15311162-T-A F2477 YY+
hg19:Y:17431741-C-T hg38:Y:15319861-C-T Y+
hg19:Y:17678133-G-A hg38:Y:15566253-G-A Y31272 YY+
hg19:Y:17723055-C-A hg38:Y:15611175-C-A Y32362 Y+
hg19:Y:17848239-G-C hg38:Y:15736359-G-C CTS8135 YY+
hg19:Y:17999606-T-C hg38:Y:15887726-T-C P7_Gap Y+
hg19:Y:18045556-T-C hg38:Y:15933676-T-C F2685 YY+
hg19:Y:18112312-G-T hg38:Y:16000432-G-T F2717 YY+
hg19:Y:18842984-A-C hg38:Y:16731104-A-C FT301980 YY+
hg19:Y:19445941-G-A hg38:Y:17334061-G-A F3054 YY+
hg19:Y:19455536-T-A hg38:Y:17343656-T-A F3056 YY+
hg19:Y:21266195-T-G hg38:Y:19104309-T-G F24073 YY+
hg19:Y:21686511-A-G hg38:Y:19524625-A-G Y31273 YY+
hg19:Y:21714436-T-C hg38:Y:19552550-T-C F3239 YY+
hg19:Y:21733531-A-G hg38:Y:19571645-A-G Y32365 YY+
hg19:Y:21790732-G-C hg38:Y:19628846-G-C FT302475 Y+
hg19:Y:22241730-A-T hg38:Y:20079844-A-T DYZ19 +
hg19:Y:22263084-G-T hg38:Y:20101198-G-T BY214661 DYZ19 +
hg19:Y:22479735-G-A hg38:Y:20317849-G-A DYZ19 +
hg19:Y:22766027-T-A hg38:Y:20604141-T-A CTS10769 Y+
hg19:Y:22770732-T-C hg38:Y:20608846-T-C CTS10776 YY+
hg19:Y:22782334-C-T hg38:Y:20620448-C-T Y+
hg19:Y:22834460-G-A hg38:Y:20672574-G-A F3360 YY+
hg19:Y:22956521-T-C hg38:Y:20794635-T-C CTS11106 YY+
hg19:Y:23075213-C-A hg38:Y:20913327-C-A Y31274 YY+
hg19:Y:23194688-G-A hg38:Y:21032802-G-A F3416 Y+
hg19:Y:23247611-T-C hg38:Y:21085725-T-C CTS11745 YY+
hg19:Y:23576293-T-C hg38:Y:21414407-T-C F3480 YY+
hg19:Y:28650882-C-T hg38:Y:26504735-C-T CTS12635 +
hg19:Y:28672414-C-T hg38:Y:26526267-C-T +

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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