Tree Position

A0-T-YP2191 > P305[A1] > A1b > BT/A1b2 > M168/PF1416[CT] > M145/P205/PF144 > M96/PF1823 > P147 > P177 > M215 > M35 > Z827 > L19 > PF2431 > Z21068

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
HG02317
2671805-C-T 2803764-C-T FT333365 Y+
2918047-T-C 3050006-T-C +
3267043-A-G 3399002-A-G +
3504130-A-G 3636089-A-G +
3659404-A-G 3791363-A-G +
3971521-G-C 4103480-G-C +
3997388-T-A 4129347-T-A +
4324362-G-A 4456321-G-A +
4624518-G-T 4756477-G-T +
4705997-T-C 4837956-T-C +
5145534-A-G 5277493-A-G +
5271447-T-C 5403406-T-C +
5422737-G-T 5554696-G-T +
5594091-A-G 5726050-A-G +
5721102-G-A 5853061-G-A +
5792291-G-A 5924250-G-A FTA48133 +
6717982-C-T 6849941-C-T Z36730 YY+
6718246-G-T 6850205-G-T Z36731 YY+
6853780-T-C 6985739-T-C Z36732 YY+
7127237-C-T 7259196-C-T Z36733 YY+
7706847-C-T 7838806-C-T Z36734 YY+
7722205-A-G 7854164-A-G FT47556 YY+
7833204-G-A 7965163-G-A BY169355 YY+
8044755-A-C 8176714-A-C FT334208 YY+
8096712-A-T 8228671-A-T FT334248 YY+
8203436-C-T 8335395-C-T FGC21764 YY+
8486301-G-A 8618260-G-A BY16794 YY+
8799031-G-A 8930990-G-A BY190237 YY+
9382010-G-T 9544401-G-T Y+
9739869-G-A 9902260-G-A IR3_Prx +
9812247-A-G 9974638-A-G FT334997 YY+
9948263-C-T 10110654-C-T Y+
9979238-C-T 10141629-C-T Y+
13240101-G-A 11084425-G-A +
13274731-G-T 11119055-G-T +
13406102-C-T 11250426-C-T +
13574683-C-T 11419007-C-T +
13693796-T-G 11538120-T-G +
13870911-C-G 11750205-C-G FTA5900 Y+
14094276-T-G 11973570-T-G FT335268 YY+
14126236-A-G 12005530-A-G Y27747 YY+
14240845-T-A 12120139-T-A FT335387 YY+
14268237-A-G 12147531-A-G FT335409 Y+
14449726-C-A 12328999-C-A FT335568 YY+
14557288-A-G 12445489-A-G FT335645 Y+
14672488-G-A 12560554-G-A FT168671 Y+
14754261-A-C 12642330-A-C FTA5943 YY+
14957524-G-A 12845599-G-A A10616A10616 YY+
15383762-A-G 13271882-A-G FT336115 YY+
15798318-C-A 13686438-C-A FT336402 YY+
15802154-C-G 13690274-C-G FT336407 YY+
15803663-G-A 13691783-G-A F20171 YY+
15847466-C-A 13735586-C-A FTA5979 YY+
15893758-G-A 13781878-G-A FTA5982 Y+
16078816-T-C 13966936-T-C FT336582 Y+
16191307-C-T 14079427-C-T FT336606 YY+
16338612-A-G 14226732-A-G FT336711 YY+
16574292-A-C 14462412-A-C FT336905 Y+
16575592-C-T 14463712-C-T FT336906 YY+
16823140-G-A 14711260-G-A FT337058 YY+
17037928-G-A 14926048-G-A YY+
17101285-G-T 14989405-G-T FT337212 YY+
17213446-G-C 15101566-G-C FT337280 Y+
17269276-G-A 15157396-G-A FT337315 Y+
17284370-A-G 15172490-A-G FTA6054 YY+
17312639-C-T 15200759-C-T FT337344 YY+
17405139-A-G 15293259-A-G FT337415 YY+
17441748-C-T 15329868-C-T YY+
17603579-C-G 15491699-C-G FT337548 YY+
17981560-T-C 15869680-T-C FT337821 Y+
18043180-T-A 15931300-T-A FTA6086 YY+
18043181-C-T 15931301-C-T FTA6087 YY+
18066850-G-A 15954970-G-A BY119627 YY+
18547213-C-A 16435333-C-A FT338090 Y+
18780516-A-C 16668636-A-C FT338254 YY+
18821046-C-T 16709166-C-T FT338277 YY+
18825756-C-T 16713876-C-T FT338279 YY+
18924568-A-G 16812688-A-G YY+
19084424-C-G 16972544-C-G FT338463 Y+
19090248-T-C 16978368-T-C FT338468 YY+
19404643-G-A 17292763-G-A FT338722 YY+
21127177-G-A 18965291-G-A BY130537 YY+
21128028-G-T 18966142-G-T FT338908 YY+
21156153-A-G 18994267-A-G FT338930 Y+
21277187-T-A 19115301-T-A FT339022 Y+
21450485-G-A 19288599-G-A FTA6197 Y+
21544786-C-T 19382900-C-T FTA6203 Y+
21876837-A-G 19714951-A-G FT339467 YY+
21993141-G-A 19831255-G-A YY+
22189865-G-T 20027979-G-T FT339672 YY+
22239196-G-T 20077310-G-T DYZ19 +
22253188-A-T 20091302-A-T DYZ19 +
22258309-G-A 20096423-G-A DYZ19 +
22270319-T-C 20108433-T-C DYZ19 +
22275775-G-A 20113889-G-A DYZ19 +
22528865-G-A 20366979-G-A FT339716 Y+
22766783-G-A 20604897-G-A FT339865 YY+
23124029-C-T 20962143-C-T FT340127 YY+
23235663-G-A 21073777-G-A FT340224 Y+
23627186-G-A 21465300-G-A FT340454 YY+
24416089-T-G 22269942-T-G FT340592 Y+
24470770-A-C 22324623-A-C FT340623 Y+
27505956-G-T 25359809-G-T P1_Y2 +
28647215-T-A 26501068-T-A +
28647219-T-C 26501072-T-C +
28701959-C-T 26555812-C-T M4394 +
28738812-G-A 26592665-G-A FT340816 +
28749165-A-G 26603018-A-G FT353971 +
28765045-A-G 26618898-A-G FT354005 +

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.