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] > P295[P] > M242[Q] > L472 > L56 > L53 > L54 > M930 > M3 > M884 > 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
HG01892
22444030-G-T 20282144-G-T FGC23102 DYZ19 +
2791092-C-T 2923051-C-T FT333415 Y+
3242520-A-G 3374479-A-G +
3408252-C-T 3540211-C-T +
3618630-T-G 3750589-T-G +
3784285-T-C 3916244-T-C +
3961482-A-G 4093441-A-G +
4077885-T-A 4209844-T-A +
4082154-G-C 4214113-G-C +
4315099-C-G 4447058-C-G +
4553561-C-A 4685520-C-A +
4667039-A-G 4798998-A-G +
4890503-A-G 5022462-A-G +
4954635-G-A 5086594-G-A +
5107473-G-A 5239432-G-A +
5110455-A-C 5242414-A-C +
5278306-G-C 5410265-G-C +
5501190-T-C 5633149-T-C +
5718738-C-T 5850697-C-T FTA25744 +
6463019-A-G 6594978-A-G +
6758908-A-G 6890867-A-G Z35742 YY+
6977559-C-T 7109518-C-T FT333628 YY+
7015110-A-T 7147069-A-T Z35743 YY+
7110511-T-G 7242470-T-G FT333699 YY+
7759936-C-G 7891895-C-G Z35744 YY+
7907496-A-G 8039455-A-G Z35745 YY+
8069112-C-A 8201071-C-A Z35746 YY+
8340278-C-G 8472237-C-G FT334399 YY+
8445741-G-A 8577700-G-A Y18634 YY+
8598227-C-T 8730186-C-T FT334581 YY+
8680385-A-G 8812344-A-G FT334653 YY+
8706451-G-A 8838410-G-A FT334675 YY+
9061479-T-C 9223870-T-C FT334881 Y+
9117253-G-A 9279644-G-A Y+
9168454-G-C 9330845-G-C Y+
9814232-C-A 9976623-C-A FT334999 YY+
13557300-C-T 11401624-C-T +
13583128-T-C 11427452-T-C +
13615903-G-A 11460227-G-A +
14161623-C-T 12040917-C-T FT335323 Y+
14316705-C-T 12195999-C-T FT335467 YY+
14506297-G-A 12394502-G-A FT335611 YY+
15146124-A-T 13034211-A-T FT335966 YY+
15260317-T-G 13148401-T-G FT336023 YY+
15492420-T-C 13380540-T-C FT336187 YY+
15589791-C-T 13477911-C-T FT336247 YY+
15770655-A-G 13658775-A-G FT336377 YY+
15773448-C-T 13661568-C-T YY+
15852079-T-G 13740199-T-G FT336431 YY+
15869544-A-G 13757664-A-G FT336440 YY+
15987568-A-C 13875688-A-C FT336515 Y+
16502382-C-A 14390502-C-A FT336853 Y+
16541094-G-A 14429214-G-A FT336879 YY+
16731464-G-A 14619584-G-A FT336998 YY+
16890047-G-T 14778167-G-T FT337094 YY+
17022540-A-T 14910660-A-T YY+
17327945-T-G 15216065-T-G FT337353 YY+
17388092-C-A 15276212-C-A FT337405 YY+
17455880-C-A 15344000-C-A FT337448 YY+
17537276-A-T 15425396-A-T FT337511 YY+
17665893-G-A 15554013-G-A FT337588 YY+
17732555-G-A 15620675-G-A FT337632 Y+
17836181-A-C 15724301-A-C Y+
17839946-G-A 15728066-G-A FT337729 Y+
18158221-C-G 16046341-C-G FT337946 Y+
18386007-G-T 16274127-G-T FT338032 P6_Gap +
18400162-C-T 16288282-C-T Y24319 P6_Gap +
18765784-A-G 16653904-A-G FT338243 YY+
18774252-C-T 16662372-C-T FT338249 YY+
19061611-C-A 16949731-C-A FT338433 YY+
19085692-T-C 16973812-T-C FT338465 Y+
19213850-C-A 17101970-C-A FT338567 YY+
19328843-C-T 17216963-C-T Y+
19382504-G-A 17270624-G-A FT338701 Y+
19398012-G-C 17286132-G-C FT338717 YY+
20809807-G-T 18647921-G-T FT348137 P4_Gap +
20825052-C-G 18663166-C-G FT348164 P4_Gap +
21297892-G-A 19136006-G-A FT339036 YY+
21366043-A-G 19204157-A-G FT339109 YY+
21557235-G-C 19395349-G-C FT339235 YY+
21633122-T-C 19471236-T-C Y+
21722779-G-A 19560893-G-A YY+
21886664-T-C 19724778-T-C FT339476 Y+
22151332-A-T 19989446-A-T Y+
22194330-G-T 20032444-G-T Y+
22239047-C-A 20077161-C-A DYZ19 +
22464021-A-G 20302135-A-G FT458292 DYZ19 +
22466065-G-A 20304179-G-A DYZ19 +
22471719-G-A 20309833-G-A DYZ19 +
22478283-G-T 20316397-G-T DYZ19 +
22486858-G-A 20324972-G-A DYZ19 +
22487969-G-C 20326083-G-C DYZ19 +
22518278-A-G 20356392-A-G FT339699 Y+
22926675-C-A 20764789-C-A FT339979 YY+
22945465-C-T 20783579-C-T FT339984 YY+
22948010-C-T 20786124-C-T FT339985 YY+
23106429-G-A 20944543-G-A Y+
23543507-C-T 21381621-C-T FT340392 YY+
23563654-G-A 21401768-G-A Y59351 YY+
23784069-T-C 21622183-T-C FT340487 Y+
23972558-A-C 21826411-A-C FT340561 Y+
23992252-C-A 21846105-C-A +
24524222-C-T 22378075-C-T P3_t2 +
28484493-C-G 26338346-C-G FT340649 +
28607153-C-T 26461006-C-T +
28789873-G-C 26643726-G-C Y81103 +

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.