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 > M925 > 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
NA19783
16998907-C-T 14887027-C-T CTS6593 Y+
14771285-G-A 12659354-G-A CTS3257 YY+
18119579-G-C 16007699-G-C CTS8633 YY+
14270176-G-T 12149470-G-T CTS2346 Y+
14027517-T-C 11906811-T-C CTS1706 YY+
2799455-T-C 2931414-T-C CTS193 YY+
3601036-T-A 3732995-T-A FT2466 +
3688688-T-C 3820647-T-C BY49000 +
4089704-C-T 4221663-C-T +
4682425-A-T 4814384-A-T +
4835282-A-G 4967241-A-G FT2582 +
5322089-C-T 5454048-C-T FT2632 +
5922901-G-A 6054860-G-A +
6060769-C-T 6192728-C-T FT2701 +
6351481-G-A 6483440-G-A BY47491 +
6362206-C-G 6494165-C-G FT326320 +
6461889-C-G 6593848-C-G FT2720 +
6461901-A-C 6593860-A-C FT2721 +
6490370-T-C 6622329-T-C FT326727 +
6931962-C-G 7063921-C-G CTS662 YY+
7144220-A-T 7276179-A-T CTS1012 YY+
7182610-G-A 7314569-G-A CTS1072 YY+
7428423-C-A 7560382-C-A FT153163 YY+
7442856-C-A 7574815-C-A CTS1499 Y+
7526745-C-T 7658704-C-T BY46936 YY+
7535352-C-G 7667311-C-G YP4673 YY+
7772807-G-A 7904766-G-A YP4674 YY+
8395921-C-T 8527880-C-T YP4675 YY+
8450581-T-C 8582540-T-C BZ4256 YY+
8509132-T-C 8641091-T-C YP4676 YY+
8557421-G-A 8689380-G-A BY47535 YY+
8901239-GTA-G 9033198-GTA-G +
9030169-G-C 9192560-G-C FT4983 Y+
9085222-C-T 9247613-C-T YP4678 Y+
9648650-T-C 9811041-T-C YP4677 IR3_Prx +
13199944-G-C 11044268-G-C BY48156 +
13345839-G-A 11190163-G-A +
13532296-G-A 11376620-G-A FT64462 +
13662258-G-A 11506582-G-A YP4679 +
13836345-C-T 11715639-C-T BY91002 +
13993721-G-C 11873015-G-C CTS1623 Y+
14007261-C-T 11886555-C-T CTS1654 Y+
14052627-G-A 11931921-G-A CTS1762 YY+
14333437-A-T 12212731-A-T CTS2508 YY+
14337584-A-T 12216879-A-T CTS2515 YY+
14483691-T-A 12362960-T-A CTS2787 YY+
14569362-G-A 12457562-G-A CTS2927 Y+
14887013-A-G 12775079-A-G CTS3392 YY+
15035760-C-T 12923848-C-T CTS3571 YY+
15156082-C-A 13044169-C-A CTS3759 YY+
15180372-C-T 13068458-C-T CTS3787 YY+
15667681-A-G 13555801-A-G CTS4481 Y+
15668116-A-G 13556236-A-G CTS4482 Y+
15679658-A-G 13567778-A-G CTS4501 Y+
15839573-C-T 13727693-C-T CTS4815 YY+
15894763-G-A 13782883-G-A CTS4904 YY+
15955087-G-A 13843207-G-A CTS5005 YY+
16025553-A-T 13913673-A-T CTS5122 Y+
16045738-C-T 13933858-C-T CTS5159 Y+
16090701-A-G 13978821-A-G CTS5255 Y+
16390248-C-T 14278368-C-T CTS5603 YY+
16610479-T-G 14498599-T-G CTS6011 YY+
16644000-C-T 14532120-C-T CTS6060 YY+
16659400-G-T 14547520-G-T CTS6084 YY+
16955964-A-G 14844084-A-G BY111381 YY+
17206622-G-A 15094742-G-A CTS6950 YY+
17291624-T-A 15179744-T-A CTS7101 YY+
17403120-G-A 15291240-G-A CTS7291 YY+
17519649-C-T 15407769-C-T CTS7522 Y+
17555115-C-A 15443235-C-A CTS7600 YY+
17680998-T-A 15569118-T-A CTS7811 YY+
17697902-T-G 15586022-T-G CTS7840 Y+
17905568-C-T 15793688-C-T CTS8265 YY+
18242409-G-A 16130529-G-A CTS8853 +
18611197-C-A 16499317-C-A YP4681 YY+
18626677-C-G 16514797-C-G CTS9032 Y+
18632292-C-A 16520412-C-A FT3109 YY+
18892594-G-T 16780714-G-T CTS9435 YY+
18909083-C-T 16797203-C-T CTS9465 YY+
18958625-C-T 16846745-C-T CTS9550 YY+
19142788-C-A 17030908-C-A CTS9912 YY+
19195460-C-T 17083580-C-T BY47208 YY+
19218783-G-A 17106903-G-A CTS10033 YY+
19352011-G-T 17240131-G-T CTS10255 Y+
19400100-A-G 17288220-A-G YY+
21213722-G-C 19051836-G-C FT298280 YY+
21230407-G-T 19068521-G-T YP4682 YY+
21416122-G-C 19254236-G-C YP4683 YY+
21521435-G-A 19359549-G-A BZ4294 YY+
21718787-C-A 19556901-C-A BY46571 YY+
21771726-A-G 19609840-A-G YP4684 YY+
21812559-C-T 19650673-C-T Y82107YP4685 YY+
21954684-G-A 19792798-G-A FT6213 YY+
21967585-C-G 19805699-C-G Y+
22217187-G-A 20055301-G-A DYZ19 +
22275491-T-G 20113605-T-G DYZ19 +
22294196-G-A 20132310-G-A BY27401 DYZ19 +
22462752-A-G 20300866-A-G FGC67700 DYZ19 +
22470825-A-G 20308939-A-G BY27829 DYZ19 +
22479324-T-A 20317438-T-A BY224218 DYZ19 +
22517511-A-T 20355625-A-T FT3221 Y+
22529584-T-A 20367698-T-A FT298942 Y+
22614883-G-C 20452997-G-C FT3227 Y+
22807063-G-A 20645177-G-A CTS10853 YY+
22891085-G-GT 20729199-G-GT +
22905230-G-A 20743344-G-A CTS11027 YY+
22926178-G-T 20764292-G-T CTS11064 YY+
23112935-C-G 20951049-C-G CTS11439 YY+
23336621-C-T 21174735-C-T CTS11895 YY+
23420061-C-A 21258175-C-A CTS12013 YY+
23451359-A-G 21289473-A-G YP4687 YY+
23740223-A-C 21578337-A-C BY45827 +
23767128-T-C 21605242-T-C YP4688 Y+
23854854-C-T 21692968-C-T YP4689 Y+
24356235-G-A 22210088-G-A F13858 +
24387499-CTA-C 22241352-CTA-C +
28609694-G-A 26463547-G-A CTS12553 Y+
28624804-T-C 26478657-T-C CTS12581 +
28634488-A-G 26488341-A-G CTS12602 +
28743097-T-C 26596950-T-C +
28749818-T-C 26603671-T-C CTS12912 +

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.