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
HG01872
6015591-G-A 6147550-G-A +
2734331-C-T 2866290-C-T F14875 YY+
2827913-T-C 2959872-T-C F14951 YY+
2859482-A-T 2991441-A-T F14972 YY8×T+
2864997-A-G 2996956-A-G F14978 YY+
2928301-C-T 3060260-C-T FT109531 +
2941945-T-A 3073904-T-A +
3031113-A-T 3163072-A-T FT315814 +
3308690-C-T 3440649-C-T FT316783 +
3343877-A-G 3475836-A-G FT316879 +
3787329-C-T 3919288-C-T +
3928015-C-T 4059974-C-T FT318967 +
4112925-A-G 4244884-A-G FT319554 +
4381316-A-G 4513275-A-G FT320475 +
4518542-C-A 4650501-C-A FT320894 +
4749091-G-A 4881050-G-A FT321632 +
5017736-C-T 5149695-C-T FT322445 +
5234916-C-T 5366875-C-T +
5543666-A-T 5675625-A-T FT324264 +
5547672-A-G 5679631-A-G FT324273 +
5559349-T-C 5691308-T-C FT324307 +
5567574-C-T 5699533-C-T FT324336 +
5632573-T-G 5764532-T-G FT324576 +
5860782-T-C 5992741-T-C FT325309 +
6414662-C-T 6546621-C-T FT326482 +
6752017-T-C 6883976-T-C Y+
6825632-T-C 6957591-T-C Y+
7176724-G-C 7308683-G-C F15656 YY+
7265817-A-G 7397776-A-G F15739 YY+
7490232-C-T 7622191-C-T IR1_L +
7548958-G-C 7680917-G-C F15940 YY+
7564739-A-G 7696698-A-G F15962 YY+
7572117-C-T 7704076-C-T F15973 YY+
7717057-A-T 7849016-A-T F16170 YY+
7909381-T-A 8041340-T-A F16411 YY+
8639143-G-T 8771102-G-T F17339 YY+
8760728-A-G 8892687-A-G FT304020 YY+
8787210-G-A 8919169-G-A F17485 YY+
8992972-T-C 9155363-T-C F17618 Y+
8998416-G-T 9160807-G-T F17625 Y+
9397291-G-A 9559682-G-A F17835 YY+
9440738-A-T 9603129-A-T FT304133 Y+
9721749-A-G 9884140-A-G IR3_Prx +
9778060-T-C 9940451-T-C Y+
9824361-C-T 9986752-C-T Y+
9912084-T-C 10074475-T-C Y+
9991999-T-A 10154390-T-A Y+
10000534-A-T 10162925-A-T Y+
10002609-C-T 10165000-C-T Y+
13131063-A-T 10620549-A-T +
13397768-A-C 11242092-A-C +
13598460-G-C 11442784-G-C +
13913343-A-G 11792637-A-G FT304188 Y+
13918047-G-A 11797341-G-A Y+
14095319-G-A 11974613-G-A F18455 YY+
14107708-C-T 11987002-C-T F18480 YY+
14110128-G-A 11989422-G-A Y+
14138873-T-A 12018167-T-A F18521 YY+
14291654-T-C 12170948-T-C Y+
14293378-C-T 12172672-C-T F18757 YY+
14300195-G-A 12179489-G-A FT304379 Y+
14492019-A-T 12380216-A-T F18996 YY+
14546836-G-A 12435037-G-A F19055 YY+
14810791-G-A 12698862-G-A F19270 YY+
15124968-A-G 13013055-A-G F19578 YY+
15300327-C-T 13188426-C-T Y+
15669873-T-C 13557993-T-C Y+
15750507-T-C 13638627-T-C F20104 YY+
15783836-CT-C 13671956-CT-C +
15873659-A-C 13761779-A-C F20235 YY+
15895490-T-C 13783610-T-C F20251 YY+
16017281-A-G 13905401-A-G Y+
16059812-C-A 13947932-C-A Y+
16512074-A-T 14400194-A-T F20767 YY+
16560428-C-G 14448548-C-G YY+
16773469-A-T 14661589-A-T F21040 YY+
16808294-T-C 14696414-T-C F21091 YY+
16985967-T-A 14874087-T-A F21275 YY+
17146438-G-C 15034558-G-C F21426 YY+
17228208-C-T 15116328-C-T Y+
17327712-G-C 15215832-G-C F21635 YY+
17352208-G-C 15240328-G-C PH3008 YY+
17482574-G-T 15370694-G-T Y+
17631865-G-A 15519985-G-A F21958 YY+
17795205-T-C 15683325-T-C F22127 YY+
17889727-G-A 15777847-G-A F22244 YY+
18406897-G-A 16295017-G-A P6_Gap +
18614359-TA-T 16502479-TA-T +
18691847-T-C 16579967-T-C F2816 YY+
18725483-A-G 16613603-A-G F22838 YY+
18787874-C-T 16675994-C-T F22909 YY+
18869923-G-A 16758043-G-A Y23321 YY+
19006266-C-A 16894386-C-A F23173 YY+
19078752-G-T 16966872-G-T F23276 YY+
19118096-T-C 17006216-T-C F23329 YY+
19164959-C-T 17053079-C-T Y+
19233920-C-T 17122040-C-T F23473 YY+
19274301-C-G 17162421-C-G F23524 YY+
19386278-T-A 17274398-T-A Y+
19431565-T-A 17319685-T-A F23679 YY+
19509422-T-C 17397542-T-C F23766 YY+
20814483-A-G 18652597-A-G FT306101 P4_Gap +
21058542-T-C 18896656-T-C Y+
21356002-A-T 19194116-A-T F24203 YY+
21382082-G-C 19220196-G-C FT306238 Y+
21453107-G-A 19291221-G-A F24319 YY+
21537119-G-A 19375233-G-A Y+
21700556-T-C 19538670-T-C F24605 YY+
21818787-G-T 19656901-G-T F24729 YY+
22031613-C-T 19869727-C-T F24949 YY+
22053098-G-A 19891212-G-A F24971 YY+
22110793-T-C 19948907-T-C F25036 YY+
22135295-G-A 19973409-G-A Y+
22157085-G-A 19995199-G-A F25079 YY+
22270228-C-G 20108342-C-G DYZ19 +
22487560-G-T 20325674-G-T DYZ19 +
22593099-T-A 20431213-T-A Y+
22614151-A-G 20452265-A-G Z44792 Y+
22708947-T-C 20547061-T-C F25381 YY+
22740145-C-T 20578259-C-T F25411 YY+
22785973-A-C 20624087-A-C F25440 YY+
22937081-A-G 20775195-A-G F25611 YY+
22999334-C-T 20837448-C-T F25676 YY+
23090987-T-C 20929101-T-C F25789 YY+
23114271-T-TA 20952385-T-TA +
23235936-G-A 21074050-G-A Y+
23278492-C-A 21116606-C-A F25924 YY+
23541769-C-T 21379883-C-T F26193 YY+
23866523-C-T 21704637-C-T F26484 Y+
24356447-A-G 22210300-A-G FT332752 +
24504156-T-C 22358009-T-C +
24636822-A-G 22490675-A-G P3_t2 +
27939666-C-A 25793519-C-A P1_Y2 +
28528460-C-G 26382313-C-G +
28601340-C-T 26455193-C-T F26752 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.