Tree Position

A0-T-YP2191 > P305[A1] > A1b > BT/A1b2 > M168/PF1416[CT] > P143[CF] > M89/PF2746[F] > F1329/M3658[GHI > F929[HIJK] > L901/M2939[H] > 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
NA21116
22471364-G-A 20309478-G-A DYZ19 +
21248052-A-G 19086166-A-G Z34577 Y+
3005484-T-C 3137443-T-C FT315717 +
3470847-A-T 3602806-A-T FT317366 +
4730034-C-G 4861993-C-G FT321581 +
4758071-G-A 4890030-G-A +
6701316-G-A 6833275-G-A BY60808 YY+
6924375-G-A 7056334-G-A FT289246 YY+
7079831-C-T 7211790-C-T Z34574 YP5955 YY+
7215060-A-T 7347019-A-T FT289322 YY+
7793697-C-A 7925656-C-A FT289481 YY+
8123375-G-T 8255334-G-T FT289595 YY+
8577355-C-G 8709314-C-G YY+
9103678-C-T 9266069-C-T Y48195 Y+
9161750-A-G 9324141-A-G FT289910 +
9344543-C-G 9506934-C-G Y+
10039379-T-A 10201770-T-A +
10046012-A-G 10208403-A-G +
10067005-A-G 10229396-A-G +
13830351-G-T 11709645-G-T FT328587 +
13848908-G-GA 11728202-G-GA +
14023380-T-C 11902674-T-C FT290044 YY+
14084411-G-A 11963705-G-A FT290065 YY+
14243388-T-C 12122682-T-C FT290140 YY+
14705323-G-C 12593389-G-C FT290292 YY+
15226580-G-T 13114666-G-T FT329535 Y+
15508116-T-C 13396236-T-C FT290503 YY+
15661901-T-C 13550021-T-C FT290550 YY+
15684143-G-C 13572263-G-C FT290555 Y+
15691019-A-C 13579139-A-C FT290557 YY+
15788440-T-C 13676560-T-C FT290593 Y+
15822117-G-C 13710237-G-C FT290609 YY+
16186762-C-T 14074882-C-T FT290684 Y+
16688607-T-A 14576727-T-A FT290847 YY+
16761817-A-G 14649937-A-G FT290872 YY+
17263174-A-T 15151294-A-T FT180997 YY+
17346283-C-A 15234403-C-A FT291053 YY+
17452764-G-A 15340884-G-A FT291094 Y+
17589287-A-T 15477407-A-T M7667 YY10×T+
17870372-T-C 15758492-T-C FT291236 YY+
17915618-C-A 15803738-C-A FT291245 YY+
18123500-T-G 16011620-T-G FT291330 YY+
19419258-C-T 17307378-C-T FT291705 YY+
21293775-A-T 19131889-A-T FT291878 YY+
21551584-T-C 19389698-T-C FT331625 YY+
21857922-G-A 19696036-G-A FT292112 YY+
21903133-T-A 19741247-T-A FT292123 YY+
22244758-G-T 20082872-G-T DYZ19 +
22362183-G-T 20200297-G-T DYZ19 +
22440128-G-A 20278242-G-A FT456414 DYZ19 +
22566452-T-A 20404566-T-A FT292264 YY+
22806490-C-G 20644604-C-G FT292342 YY+
23108045-A-T 20946159-A-T Y+
23151080-T-C 20989194-T-C FT292453 YY+
23225528-A-T 21063642-A-T FT292476 Y+
23811565-G-A 21649679-G-A FT292625 Y+
24466510-A-G 22320363-A-G Y+
28749166-A-C 26603019-A-C FT292781 +

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.