Tree Position

R-P312/S116 > Z40481 > ZZ11 > U152/S28 > L2/S139 > Z41150 > Z49 > A21822 > Y18901

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 STRFTDNA
28590046-G-A 26443899-G-A Y80916 +
23464372-G-A 21302486-G-A Y79917 YY+
16992989-G-A 14881109-G-A Y70874 YY+
17947369-C-T 15835489-C-T Y72702 YY+
17951191-GAA-G 15839311-GAA-G +
18833966-G-T 16722086-G-T Y74117 YY+
18999034-G-A 16887154-G-A Y74408 YY+
19224426-G-A 17112546-G-A Y74916 YY+
23614738-G-A 21452852-G-A Y80183 YY+
21531967-T-C 19370081-T-C Y76695 YY+
15132914-G-T 13021001-G-T Y67782 YY+
21822613-G-A 19660727-G-A Y77207 YY+
22183488-T-A 20021602-T-A Y77906 YY+
22202779-A-T 20040893-A-T Y77944 YY8×T+
23116305-G-C 20954419-G-C Y79278 YY+
22246459-C-G 20084573-C-G DYZ19 +
23074991-C-T 20913105-C-T Y79206 YY+
23056948-G-A 20895062-G-A Y79145 YY+
16744770-G-C 14632890-G-C Y70417 YY+
16855898-G-T 14744018-G-T Y70620 YY+
13812603-C-T 11691897-C-T Y65518 +
8679773-T-G 8811732-T-G Y64324 YY+
4863043-G-A 4995002-G-A BY42637 +
6634466-A-C 6766425-A-C Y60735 YY+
6753775-A-G 6885734-A-G Y60912 YY+
7633314-G-C 7765273-G-C Y62274 YY+
7805361-A-G 7937320-A-G Y62592 YY+
7748466-T-A 7880425-T-A Y62498 YY+
9414930-G-A 9577321-G-A Y65024 YY+
9405156-G-A 9567547-G-A Y65010 YY+
10017302-C-T 10179693-C-T BY42889 **
22448953-T-A 20287067-T-A DYZ19 **
4357234-G-A 4489193-G-A BY42631 **
28024580-T-G 25878433-T-G BY152266 P1_Y2 **
25220225-C-T 23074078-C-T P2_r1 ***
24332102-C-T 22185955-C-T P3_t1 ***
24839989-G-A 22693842-G-A IR1_R ***
24138846-T-C 21992699-T-C P3_b1 ***
25027143-T-A 22880996-T-A g1 ***
25937795-A-C 23791648-A-C P1_Y1 ***
25994198-C-T 23848051-C-T P1_Y1 ***
26233443-G-T 24087296-G-T P1_Y1 ***
22454004-G-A 20292118-G-A DYZ19 ***
22451633-G-A 20289747-G-A DYZ19 ***
24831384-T-TA 22685237-T-TA P3_b2 12×A***
22446363-G-A 20284477-G-A BY152265 DYZ19 ***
18089066-AT-A 15977186-AT-A ***
22243678-C-G 20081792-C-G Z11133 DYZ19 ***
26187192-G-A 24041045-G-A P1_Y1 ***
28795604-G-A 26649457-G-A BY151500 ***
6178727-T-A 6310686-T-A IR3_Dst ***
9372226-A-G 9534617-A-G ***
13318658-G-A 11162982-G-A ***
18309894-T-C 16198014-T-C P6_Prx ***
22345437-A-T 20183551-A-T DYZ19 ***
13806561-AGAATG-A 11685855-AGAATG-A 7×GAATG***
19886412-G-A 17774532-G-A P5_Prx ***
19895462-T-C 17783582-T-C P5_Prx ***
22227136-T-C 20065250-T-C DYZ19 ***
22302151-T-G 20140265-T-G FT252943 DYZ19 ***
22302356-T-C 20140470-T-C DYZ19 ***
22305046-T-G 20143160-T-G DYZ19 ***
19669573-A-AG 17557693-A-AG P5_Prx ***

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)

Kit: 4888551078194378252817912285
Used in age calculations1078194378252817912285
Counts of SNPs2525
Variant counts last updated 2020-07-20 02:38:31.

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