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
HG02259
28497849-T-A 26351702-T-A BY28200 Y80877 Y+
21084436-TA-T 18922550-TA-T +
2789736-A-G 2921695-A-G FT333414 Y+
2885774-T-G 3017733-T-G Z35706 YY+
3034339-G-T 3166298-G-T +
3355371-T-C 3487330-T-C +
3682866-C-T 3814825-C-T +
4620368-G-T 4752327-G-T +
4638793-C-T 4770752-C-T FGC52854 +
4687476-C-T 4819435-C-T +
4859786-G-A 4991745-G-A +
4946920-T-C 5078879-T-C +
5013917-C-G 5145876-C-G +
5112497-G-A 5244456-G-A FT78328 +
5534482-T-C 5666441-T-C +
5631540-G-A 5763499-G-A +
5656538-A-G 5788497-A-G +
6105209-T-C 6237168-T-C FT391409 +
6372898-G-A 6504857-G-A +
6656860-A-G 6788819-A-G Z35707 YY+
6685144-G-T 6817103-G-T FT333501 Y+
6755114-T-G 6887073-T-G FT333537 YY+
6854077-T-C 6986036-T-C Z35708 YY+
6924864-T-G 7056823-T-G Z35710 YY+
6925902-T-C 7057861-T-C Y+
7058026-T-C 7189985-T-C FT333670 YY+
7240954-T-C 7372913-T-C FT333774 Y+
7632444-G-A 7764403-G-A FTA5823 Y+
7647943-C-G 7779902-C-G FT333973 YY+
7795714-G-A 7927673-G-A FT334055 YY+
8043797-C-G 8175756-C-G Y+
8095798-A-G 8227757-A-G FT179233 YY+
8329496-T-G 8461455-T-G FT334389 YY+
8611446-A-G 8743405-A-G FT334593 YY+
8995251-C-T 9157642-C-T FT334838 Y+
9019453-C-A 9181844-C-A FT334859 Y+
9172902-A-G 9335293-A-G Y+
9802897-A-C 9965288-A-C Y+
9851395-G-C 10013786-G-C YY+
13465549-A-G 11309873-A-G +
13511708-C-A 11356032-C-A +
13800039-T-C 11679333-T-C +
13938577-G-A 11817871-G-A FT192832 Y+
13982785-T-C 11862079-T-C FT335175 Y+
14027287-C-T 11906581-C-T FT335220 YY+
14086290-G-A 11965584-G-A FT335264 Y+
14118908-G-A 11998202-G-A FTA5918 Y+
14166794-A-C 12046088-A-C Y+
14400375-A-G 12279672-A-G FT335531 YY+
14406906-C-G 12286204-C-G FT335534 YY+
14492909-C-T 12381106-C-T FT335605 Y+
14792496-T-C 12680567-T-C FT335772 YY+
14830527-A-G 12718594-A-G FT335795 YY+
15194183-A-G 13082269-A-G FT335994 YY+
15349440-A-G 13237559-A-G FT336090 YY+
15594638-G-A 13482758-G-A FT336250 YY+
15834266-G-C 13722386-G-C FT336427 YY+
15963596-C-T 13851716-C-T FT336496 Y+
15995958-G-C 13884078-G-C FT336525 YY+
16518178-T-G 14406298-T-G FT336861 YY+
16576300-T-G 14464420-T-G FT336907 YY+
16629610-C-G 14517730-C-G FT336937 YY+
16694671-T-C 14582791-T-C FT336981 YY+
16744119-A-G 14632239-A-G FT337003 YY+
16979735-T-G 14867855-T-G FT337139 Y+
17141805-C-T 15029925-C-T FT337237 YY+
17373090-T-C 15261210-T-C FT337393 Y+
17437374-C-T 15325494-C-T FT337437 YY+
17679292-C-T 15567412-C-T BY116610 YY+
18081489-G-A 15969609-G-A FT337884 YY+
18129709-C-T 16017829-C-T FT337928 YY+
18202490-T-C 16090610-T-C FT337988 YY+
18707360-A-C 16595480-A-C FT338201 YY+
18843474-G-C 16731594-G-C FT338293 YY+
18858207-C-A 16746327-C-A FT338304 YY+
18878114-G-T 16766234-G-T FT338317 Y+
18925795-A-G 16813915-A-G FT338343 YY+
19097294-C-T 16985414-C-T FGC57383 YY+
19324049-C-A 17212169-C-A FT338655 YY+
19427656-G-T 17315776-G-T FT338743 Y+
19555754-G-A 17443874-G-A FT291740 Y+
21054015-G-T 18892129-G-T FT338862 YY+
21191405-G-A 19029519-G-A FT338943 YY+
21567307-C-T 19405421-C-T FT262039 YY+
21993321-T-G 19831435-T-G FT339542 YY+
22144704-A-G 19982818-A-G FT339638 YY+
22263026-A-C 20101140-A-C DYZ19 +
22458070-C-G 20296184-C-G DYZ19 +
22473859-C-T 20311973-C-T DYZ19 +
22483054-T-G 20321168-T-G DYZ19 +
22511552-G-C 20349666-G-C DYZ19 +
22512773-A-C 20350887-A-C DYZ19 +
22912670-G-C 20750784-G-C FT339969 YY+
23121101-G-T 20959215-G-T YY+
23306525-T-G 21144639-T-G FT340261 YY+
23396732-C-A 21234846-C-A YY+
28690423-C-T 26544276-C-T FT340780 +
28785008-G-T 26638861-G-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.