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] > M2335 > F346[NO] > P191[O] > 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
HG00478
13677194-T-G 11521518-T-G BY43168 +
8826899-G-C 8958858-G-C Y+
2771798-A-G 2903757-A-G CTS156 Y+
2840738-A-G 2972697-A-G CTS247 YY+
3017751-G-A 3149710-G-A FT315768 +
3726220-T-C 3858179-T-C FT318271 +
4145991-G-A 4277950-G-A +
4216042-A-G 4348001-A-G FT319919 +
4263293-T-C 4395252-T-C FT320068 +
4294831-G-T 4426790-G-T FT320181 +
4644032-C-T 4775991-C-T FT321288 +
4707931-T-A 4839890-T-A FT321489 +
4876729-G-A 5008688-G-A FT321975 +
5054593-A-C 5186552-A-C FT322561 +
5200294-G-A 5332253-G-A +
5363445-A-G 5495404-A-G FT323653 +
5474079-A-G 5606038-A-G FT324031 +
5576681-C-T 5708640-C-T FT324365 +
5875981-C-T 6007940-C-T FT145492 +
6050696-T-C 6182655-T-C FT325974 +
6078355-C-T 6210314-C-T FT326068 +
6385183-G-A 6517142-G-A +
6791806-C-G 6923765-C-G F15333 YY+
6880735-G-A 7012694-G-A YY+
7246823-A-T 7378782-A-T F15717 YY+
7567837-G-A 7699796-G-A YY+
7605129-G-A 7737088-G-A F16011 YY+
7800006-T-C 7931965-T-C F16264 YY+
8113099-T-A 8245058-T-A YY+
8228872-T-C 8360831-T-C F16787 YY+
8241079-T-G 8373038-T-G F16805 YY+
8336331-C-T 8468290-C-T F16915 YY+
8547028-C-T 8678987-C-T F17213 YY+
8582402-T-A 8714361-T-A F17264 YY+
8591711-G-C 8723670-G-C FT295441 YY+
8768727-C-T 8900686-C-T F17465 YY+
9091187-C-T 9253578-C-T F17726 Y+
9424029-A-G 9586420-A-G YY+
9760811-G-C 9923202-G-C Y+
10006901-G-A 10169292-G-A Y+
10055025-G-A 10217416-G-A +
13207397-G-A 11051721-G-A +
13503013-G-T 11347337-G-T +
13849736-G-A 11729030-G-A FT146244 +
13854713-G-A 11734007-G-A FT328775 +
13865061-G-C 11744355-G-C +
13940801-C-T 11820095-C-T FT123930 Y+
14049916-T-A 11929210-T-A YY+
14185332-T-C 12064626-T-C YY+
14255915-G-A 12135209-G-A FT296056 Y+
14381685-G-A 12260981-G-A FT296128 Y+
14428256-T-C 12307531-T-C YY+
14496176-T-C 12384373-T-C F19002 YY+
14977212-C-G 12865287-C-G CTS3500 YY+
15064259-G-T 12952351-G-T BZ4109 YY+
15305238-T-C 13193337-T-C F19686 YY+
15567575-T-C 13455695-T-C CTS4313 YY+
15665772-G-A 13553892-G-A YY+
15765877-T-C 13653997-T-C CTS4682 YY+
16200404-G-A 14088524-G-A CTS5309 YY+
16328334-A-C 14216454-A-C F20572 YY+
16434127-T-A 14322247-T-A F20684 YY+
16484779-C-T 14372899-C-T CTS5795 YY+
16717115-T-C 14605235-T-C F20978 YY+
17163343-C-T 15051463-C-T Y+
17249075-A-G 15137195-A-G FT297197 Y+
17258584-C-G 15146704-C-G Y+
17273027-G-T 15161147-G-T F21548 YY+
17655812-C-T 15543932-C-T F21983 YY+
17724148-A-G 15612268-A-G FT297382 Y+
17853502-C-T 15741622-C-T F22200 YY+
17920617-T-C 15808737-T-C CTS8290 YY+
18421476-A-T 16309596-A-T P6_Gap +
18563321-C-T 16451441-C-T CTS8935 YY+
18755526-C-G 16643646-C-G CTS9221 YY+
18756642-C-A 16644762-C-A F22874 YY+
18950202-C-T 16838322-C-T F23102 YY+
18950607-G-C 16838727-G-C CTS9532 YY+
19037171-C-T 16925291-C-T CTS9719 YY+
19170776-G-C 17058896-G-C Y+
19400088-T-C 17288208-T-C YY+
19496450-A-G 17384570-A-G YY+
21315313-T-G 19153427-T-G F24145 YY+
21351314-C-T 19189428-C-T FT252436 Y+
21571729-C-T 19409843-C-T F24463 YY+
21744592-G-A 19582706-G-A FT298633 Y+
21817303-G-C 19655417-G-C F24726 YY+
22478608-G-T 20316722-G-T DYZ19 +
22485254-G-A 20323368-G-A DYZ19 +
22651393-G-C 20489507-G-C FTA3841 YY+
22828039-C-T 20666153-C-T CTS10905 YY+
23096816-G-A 20934930-G-A FT299209 YY+
23160663-G-C 20998777-G-C CTS11558 Y+
23329304-C-A 21167418-C-A YY+
23334612-A-G 21172726-A-G CTS11889 YY+
23401107-T-C 21239221-T-C CTS11978 Y+
23515117-G-A 21353231-G-A F26160 YY+
23621102-T-C 21459216-T-C F26306 YY+
24484455-T-C 22338308-T-C +
28461676-CG-C 26315529-CG-C +
28498172-T-C 26352025-T-C FT299591 Y+
28544729-C-T 26398582-C-T FT299635 +
28594072-G-A 26447925-G-A FT299655 +
28631750-A-G 26485603-A-G CTS12596 Y+

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.