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 > J > J1 > Z2215 > Z2217 > Y3473 > 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.

POS-REF-ALT (hg19) POS-REF-ALT (hg38) Blocks Names Region McDonald BED combBED STR1kG
HG01494
7233156-A-G 7365115-A-G CTS1141 YY+
16224446-C-A 14112566-C-A CTS5363 YY+
2870585-G-T 3002544-G-T YY+
3129932-C-T 3261891-C-T ZS2762 +
3346417-G-T 3478376-G-T ZS2764 +
3521680-T-A 3653639-T-A ZS2766 +
3634164-A-T 3766123-A-T ZS2767 +
3645070-C-A 3777029-C-A ZS2768 +
3676778-G-A 3808737-G-A ZS2769 +
3888353-A-T 4020312-A-T ZS2772 +
4012048-C-T 4144007-C-T ZS2774 +
4740597-C-A 4872556-C-A ZS2779 +
6030873-A-G 6162832-A-G ZS2786 +
6511284-T-C 6643243-T-C ZS2791 +
6528505-A-T 6660464-A-T ZS2792 +
6536772-C-A 6668731-C-A ZS2793 +
6739448-A-G 6871407-A-G ZS2794 YY+
6764073-T-A 6896032-T-A CTS461 YY+
7038497-G-A 7170456-G-A ZS2797 YY+
7233327-A-G 7365286-A-G CTS1142 YY+
7357038-T-C 7488997-T-C CTS1354 YY+
7459849-A-C 7591808-A-C CTS1519 IR1_L +
7877358-C-T 8009317-C-T Z1831 YY+
7887920-T-C 8019879-T-C ZS2801 YY+
7978315-G-A 8110274-G-A ZS2802 YY+
8170554-G-T 8302513-G-T ZS2804 YY+
8378478-A-G 8510437-A-G ZS2806 YY+
8734551-C-A 8866510-C-A ZS2809 YY+
8757939-T-A 8889898-T-A ZS2810 YY+
8775973-A-T 8907932-A-T ZS2811 YY+
9046036-C-A 9208427-C-A ZS2812 Y+
9820427-A-T 9982818-A-T ZS2814 YY+
9977959-T-C 10140350-T-C ZS2815 Y+
13206218-G-T 11050542-G-T ZS2817 +
13351525-G-T 11195849-G-T ZS2818 +
14563608-C-A 12451808-C-A ZS2823 Y+
14647204-G-A 12535269-G-A CTS3078 YY+
14869180-G-A 12757250-G-A CTS3367 YY+
15217755-T-A 13105841-T-A CTS3835 Y+
15360352-C-A 13248472-C-A ZS2825 YY+
15481466-C-G 13369586-C-G CTS4212 YY+
15691957-G-T 13580077-G-T CTS4520 YY+
16055137-C-G 13943257-C-G ZS2828 Y+
16240481-A-T 14128601-A-T CTS5378 YY+
16252645-C-G 14140765-C-G Z1835 CTS5403 YY+
16681137-T-C 14569257-T-C ZS2831 YY+
16922903-G-A 14811023-G-A Y4364Y4372 M12159 YY+
16991572-A-G 14879692-A-G CTS6580 YY+
17162788-C-G 15050908-C-G Z1837 CTS6872 Y+
17340718-C-T 15228838-C-T CTS7188 YY+
17539207-T-G 15427327-T-G ZS2835 Y+
17796779-C-A 15684899-C-A CTS8016 Y+
17921696-C-A 15809816-C-A ZS2836 YY+
17921715-C-A 15809835-C-A ZS2837 YY+
18060253-T-C 15948373-T-C YY+
21234530-G-T 19072644-G-T ZS2845 YY+
21328527-G-A 19166641-G-A ZS2847 YY+
21404829-C-T 19242943-C-T ZS2849 YY+
21504503-G-A 19342617-G-A ZS2851 YY+
21849934-G-A 19688048-G-A ZS2855 Y+
22043684-C-A 19881798-C-A ZS2858 YY+
22136047-A-G 19974161-A-G ZS2859 YY+
22218979-C-A 20057093-C-A ZS2860 DYZ19 +
22469764-C-T 20307878-C-T ZS2861 DYZ19 +
22471606-C-T 20309720-C-T ZS2862 DYZ19 +
22629677-G-A 20467791-G-A ZS2864 Y+
23303571-C-T 21141685-C-T CTS11836 YY+

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.