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 > Z5908 > Z19318 > Z5910 > 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
HG02277
17466998-A-G 15355118-A-G Y26835 YY+
2980525-T-C 3112484-T-C +
3049292-G-A 3181251-G-A +
3197100-G-T 3329059-G-T +
3470542-C-A 3602501-C-A +
3522891-T-C 3654850-T-C +
3766384-G-A 3898343-G-A +
4295974-G-C 4427933-G-C 7425426-G-AFT56965 +
4381223-C-G 4513182-C-G +
5195880-G-C 5327839-G-C +
5465484-T-C 5597443-T-C +
5807828-G-C 5939787-G-C +
5907954-G-C 6039913-G-C +
5948340-A-C 6080299-A-C +
5999161-C-G 6131120-C-G +
6385664-G-A 6517623-G-A +
6737951-C-G 6869910-C-G Z35891 YY+
6830442-G-A 6962401-G-A FT226167 Y+
6951036-T-A 7082995-T-A Z35892 YY+
7094400-C-T 7226359-C-T FTA5813 YY+
7277859-C-T 7409818-C-T Z35894 YY+
7321388-T-G 7453347-T-G Z35895 YY+
7571498-T-C 7703457-T-C FT333922 YY+
7635182-C-T 7767141-C-T FT333958 YY+
7737090-C-A 7869049-C-A FT334021 YY+
7832558-C-T 7964517-C-T FT334074 YY+
7853088-T-C 7985047-T-C FTA5830 YY+
7950615-A-G 8082574-A-G FT334147 YY+
8112574-A-G 8244533-A-G FTA5842 YY+
8283131-G-A 8415090-G-A FT334360 YY+
8378501-G-A 8510460-G-A FT334425 YY+
8534753-A-G 8666712-A-G FT334533 YY+
8651858-T-C 8783817-T-C FT334623 YY+
8733418-T-C 8865377-T-C FT334697 Y+
8867878-C-T 8999837-C-T FT334780 Y+
9040252-C-T 9202643-C-T FT334869 Y+
9045312-C-G 9207703-C-G FT334871 Y+
9466048-A-C 9628439-A-C +
9845694-T-G 10008085-T-G FT335022 YY+
9921426-A-G 10083817-A-G Y+
13211636-C-T 11055960-C-T PF7439 +
13298714-C-A 11143038-C-A +
13383711-G-A 11228035-G-A +
13594693-C-A 11439017-C-A +
13881909-A-G 11761203-A-G FT335067 Y+
13990447-G-A 11869741-G-A BY76984Y65717 YY+
14064109-A-G 11943403-A-G FT335245 YY+
14077908-G-T 11957202-G-T FT335257 YY+
14080723-A-T 11960017-A-T FT335260 YY+
14124069-G-T 12003363-G-T FT335287 YY+
14282669-G-T 12161963-G-T Y131319 YY+
14365420-A-G 12244715-A-G FT335508 YY+
14480815-C-T 12360084-C-T FT335588 YY+
14908799-C-G 12796866-C-G FT335836 Y+
15219502-T-C 13107588-T-C FT336009 Y+
15232130-G-T 13120216-G-T Y+
15248272-G-T 13136358-G-T FT336019 Y+
15395068-A-T 13283188-A-T FT336125 Y+
15451322-C-A 13339442-C-A FT336165 YY+
15506833-C-T 13394953-C-T FT336199 YY+
15576847-A-G 13464967-A-G FT336242 YY+
15606041-C-T 13494161-C-T FT336266 YY+
15694870-T-C 13582990-T-C FT336304 YY+
15699243-G-A 13587363-G-A FT336311 Y+
16276017-T-G 14164137-T-G FT336676 YY+
16439456-G-A 14327576-G-A BY162145 YY+
16555827-G-A 14443947-G-A FT336889 YY+
16847552-A-G 14735672-A-G FTA6031 YY+
16896736-C-T 14784856-C-T FT337095 YY+
17033570-T-C 14921690-T-C FT337175 YY+
17200908-G-T 15089028-G-T FT337265 YY+
17521939-C-G 15410059-C-G Y+
18218462-G-A 16106582-G-A FT338000 Y+
18227074-C-T 16115194-C-T +
18243865-C-T 16131985-C-T Y+
18391920-T-G 16280040-T-G FT338038 P6_Gap +
18605273-T-C 16493393-T-C FT338123 YY+
18864944-T-C 16753064-T-C FTA6122 YY+
18918471-C-T 16806591-C-T Y74269 YY+
18941413-G-T 16829533-G-T FT338355 YY+
19065307-C-G 16953427-C-G FT338434 Y+
19398750-A-G 17286870-A-G FT338720 YY+
21353705-C-T 19191819-C-T FT339094 YY+
21367563-G-A 19205677-G-A FT97082 YY+
21670549-A-G 19508663-A-G Y+
21718992-C-T 19557106-C-T FT339341 YY+
22201720-A-C 20039834-A-C FT339678 YY+
22214723-T-A 20052837-T-A FT339691 Y+
22293567-C-T 20131681-C-T DYZ19 +
22457783-T-C 20295897-T-C BY25431 DYZ19 +
22479204-T-C 20317318-T-C BY224184 DYZ19 +
22530962-A-G 20369076-A-G Y+
22621624-C-A 20459738-C-A Y+
22779029-G-A 20617143-G-A FT339873 Y+
22989890-C-T 20828004-C-T FT340011 Y+
23008549-C-A 20846663-C-A FT340027 Y+
23093368-A-G 20931482-A-G FT340100 Y+
23242046-C-T 21080160-C-T YY+
23280638-G-A 21118752-G-A FTA6277 YY+
23450726-T-G 21288840-T-G FT340339 YY+
23456987-G-A 21295101-G-A YY+
23642045-T-C 21480159-T-C Y+
23779008-C-G 21617122-C-G FT340483 Y+
23983511-A-G 21837364-A-G FT340570 Y+
23997101-G-A 21850954-G-A Y+
24875395-T-C 22729248-T-C g1 +
28587476-C-T 26441329-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.