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 > Z8028 > 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
HG02304
2943118-C-T 3075077-C-T +
3122983-C-A 3254942-C-A +
3258916-C-G 3390875-C-G +
3656501-C-T 3788460-C-T +
4191237-A-G 4323196-A-G +
4552550-T-C 4684509-T-C +
4587674-T-C 4719633-T-C +
4907926-C-G 5039885-C-G +
4916593-C-T 5048552-C-T +
5440192-C-T 5572151-C-T +
5855008-T-C 5986967-T-C +
5874006-C-T 6005965-C-T +
6350995-G-T 6482954-G-T +
6474573-T-C 6606532-T-C +
6483518-C-T 6615477-C-T +
6494511-T-A 6626470-T-A +
6495019-A-T 6626978-A-T +
6540449-A-G 6672408-A-G +
6596621-A-G 6728580-A-G +
6665352-T-C 6797311-T-C FT333490 Y+
6824881-A-G 6956840-A-G Z35928 YY+
6958107-T-C 7090066-T-C Z35929 YY+
6976211-T-C 7108170-T-C FGC82973 Y+
7060552-A-G 7192511-A-G Y+
7096479-G-A 7228438-G-A Z35930 YY+
7208319-C-T 7340278-C-T FT333755 YY+
7426159-A-T 7558118-A-T Z35931 YY+
7704323-G-A 7836282-G-A Z35932 YY+
7814518-T-A 7946477-T-A YY+
7822426-A-T 7954385-A-T YY+
8016561-G-A 8148520-G-A YY+
8249571-T-A 8381530-T-A FT334346 YY+
8298058-G-A 8430017-G-A YY+
8370058-T-C 8502017-T-C Y+
8449247-G-A 8581206-G-A YY+
8474837-G-T 8606796-G-T YY+
8569711-T-A 8701670-T-A YY+
8621072-C-A 8753031-C-A FT334596 YY+
8659862-A-C 8791821-A-C FT334632 YY+
8724916-C-T 8856875-C-T FT334690 Y+
9166391-C-A 9328782-C-A FT334948 Y+
9380828-G-A 9543219-G-A Y+
9871769-C-T 10034160-C-T BY81654 YY+
10024850-C-G 10187241-C-G Y+
10041028-G-C 10203419-G-C +
13224708-C-A 11069032-C-A +
13338495-G-T 11182819-G-T +
13459487-G-A 11303811-G-A +
13520393-C-G 11364717-C-G +
13623563-C-T 11467887-C-T +
13660330-G-T 11504654-G-T BY87403 +
13660331-G-T 11504655-G-T +
13675743-G-A 11520067-G-A +
13700793-G-C 11545117-G-C +
13717285-G-T 11561609-G-T +
13803531-C-T 11682825-C-T +
13811678-G-A 11690972-G-A +
13831378-C-T 11710672-C-T +
13873883-A-G 11753177-A-G FT335057 Y+
13936819-G-A 11816113-G-A FT248818 Y+
14210524-G-A 12089818-G-A FT335363 YY+
14280145-C-T 12159439-C-T FT335427 YY+
14484048-G-A 12363317-G-A Y91550 YY+
14537255-C-T 12425456-C-T BY96367 YY+
14604834-T-A 12493036-T-A FT335676 YY+
14877353-A-G 12765423-A-G YY+
14939228-C-A 12827302-C-A FT335859 YY+
15534615-T-C 13422735-T-C FT336215 YY+
15709291-C-G 13597411-C-G FT336322 YY+
15850813-G-A 13738933-G-A YY+
15892368-G-A 13780488-G-A FT336453 Y+
16195719-G-A 14083839-G-A FT336608 YY+
16203492-G-A 14091612-G-A FT336614 YY+
16233118-G-A 14121238-G-A FT336640 YY+
16288564-A-G 14176684-A-G YY+
16292008-G-A 14180128-G-A FT336682 YY+
16341612-C-G 14229732-C-G FT336714 YY+
16398169-C-T 14286289-C-T FT336754 Y+
16416378-C-T 14304498-C-T BY107646 YY+
16488709-T-C 14376829-T-C FT336843 YY+
16764708-A-C 14652828-A-C FT337018 YY+
16767423-G-T 14655543-G-T FT337022 YY+
17073304-G-A 14961424-G-A FT337196 YY+
17132709-C-T 15020829-C-T YY+
17184462-C-T 15072582-C-T FT201864 YY+
17239742-G-A 15127862-G-A YY+
17424632-A-G 15312752-A-G FT337429 YY+
17778507-A-G 15666627-A-G FT337678 Y+
18019384-C-G 15907504-C-G FT337834 Y+
18136131-C-T 16024251-C-T FT337931 YY+
18237366-G-A 16125486-G-A Y+
18398394-T-C 16286514-T-C FT338045 P6_Gap +
18400252-G-A 16288372-G-A FGC65227 P6_Gap +
18641163-A-C 16529283-A-C YY+
18659091-G-A 16547211-G-A FT338172 YY+
18755342-C-T 16643462-C-T FT338233 YY+
19124209-C-T 17012329-C-T FT338501 YY+
19289158-G-A 17177278-G-A FT338623 YY+
21303365-C-T 19141479-C-T FT339044 YY+
21363852-C-T 19201966-C-T FT339106 YY+
21380902-G-T 19219016-G-T FT339125 Y+
21522371-G-A 19360485-G-A FT339205 Y+
21527026-A-T 19365140-A-T FT339213 YY+
21545061-T-C 19383175-T-C FT339227 Y+
21598102-T-C 19436216-T-C FT339268 Y+
21644912-C-T 19483026-C-T FT339295 YY+
21693241-T-C 19531355-T-C FT339326 YY+
22164495-C-G 20002609-C-G FT339655 YY+
22473810-T-A 20311924-T-A DYZ19 +
22474174-T-A 20312288-T-A DYZ19 +
22579033-G-C 20417147-G-C FT339753 YY+
22642498-A-G 20480612-A-G FT339791 Y+
22650838-A-C 20488952-A-C FT339798 YY+
23078305-C-A 20916419-C-A FT340084 Y+
23480327-G-A 21318441-G-A YY+
23523805-C-T 21361919-C-T YY+
23599832-A-T 21437946-A-T FT340433 YY+
23744194-A-G 21582308-A-G +
23796687-T-G 21634801-T-G FT340500 Y+
24112598-T-C 21966451-T-C P3_b1 +
24497510-C-A 22351363-C-A +
24508066-A-C 22361919-A-C FT344762 +
28529372-A-G 26383225-A-G +
28688038-C-T 26541891-C-T +

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.