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
NA18548
5707172-G-C 5839131-G-C FT324831 +
3087620-T-C 3219579-T-C FT197558 +
3482129-T-A 3614088-T-A FT317405 +
3725619-T-C 3857578-T-C +
3784485-G-A 3916444-G-A FT318481 +
3948759-C-G 4080718-C-G FT319023 +
4262767-T-C 4394726-T-C FT320067 +
4522798-T-G 4654757-T-G +
4525725-G-T 4657684-G-T +
4683294-A-T 4815253-A-T FT321392 +
4809270-G-T 4941229-G-T +
4842799-G-A 4974758-G-A +
5047660-C-T 5179619-C-T PF4235 FT197898 +
5274156-G-A 5406115-G-A FT323351 +
5396089-C-T 5528048-C-T FT323755 +
5458055-T-C 5590014-T-C +
5619822-C-T 5751781-C-T FT324533 +
5676401-G-T 5808360-G-T +
5841732-T-C 5973691-T-C +
5875063-G-T 6007022-G-T +
6449229-G-A 6581188-G-A FT326590 +
6668614-A-G 6800573-A-G MF2636 YY+
6686088-A-G 6818047-A-G Y+
6708295-G-A 6840254-G-A F15272 YY+
6716445-T-A 6848404-T-A CTS374 YY+
6811189-C-T 6943148-C-T MF2637 YY+
6824525-C-T 6956484-C-T F15362 YY+
6991252-G-A 7123211-G-A SK1720 YY+
7348986-A-T 7480945-A-T FT300127 Y+
7402549-C-T 7534508-C-T FT300139 YY+
8518188-C-G 8650147-C-G MF2639 YY+
8617832-C-G 8749791-C-G SK1717 YY+
8894754-A-C 9026713-A-C F17594 Y+
9131277-C-T 9293668-C-T F17780 Y+
9151820-G-A 9314211-G-A F17806 Y+
9157929-T-C 9320320-T-C FT300647 +
9382054-T-C 9544445-T-C DC145 Y+
9645015-G-T 9807406-G-T IR3_Prx +
9790850-C-T 9953241-C-T MF2640 Y+
9800907-T-G 9963298-T-G Y+
9823581-A-C 9985972-A-C MF1380 YY+
10094531-A-T 10256922-A-T +
13293591-C-T 11137915-C-T +
13427202-C-T 11271526-C-T +
13461371-T-A 11305695-T-A +
13485150-G-T 11329474-G-T +
13549699-A-C 11394023-A-C +
13603834-G-T 11448158-G-T +
13801948-C-T 11681242-C-T BY41375 +
14323175-T-C 12202469-T-C F18799 YY+
14433102-G-A 12312375-G-A CTS2695 Y+
14489900-G-A 12369169-G-A MF1381 YY+
14596172-A-G 12484372-A-G F19097 YY+
15039932-C-G 12928022-C-G F19495 YY+
15243778-C-G 13131864-C-G Y+
15284232-T-A 13172331-T-A Y+
15618723-A-G 13506843-A-G MF2643 YY+
15791407-T-C 13679527-T-C YY+
15832891-C-T 13721011-C-T F20202 YY+
15926111-T-G 13814231-T-G CTS4960 YY+
16264413-A-G 14152533-A-G MF1383 YY+
16455735-C-G 14343855-C-G F20703 YY+
16542194-C-T 14430314-C-T MF1384 YY+
16621278-C-T 14509398-C-T CTS6029 Y+
16872845-A-G 14760965-A-G CTS6401 YY+
16976373-A-G 14864493-A-G Y+
17087773-T-C 14975893-T-C CTS6741 Y+
17088876-C-G 14976996-C-G CTS6749 YY+
17261059-C-A 15149179-C-A CTS7054 Y+
17273503-C-T 15161623-C-T CTS7081 YY+
17595491-C-A 15483611-C-A F21925 YY+
17789934-C-T 15678054-C-T CTS7996 YY+
17921659-G-A 15809779-G-A F22284 YY+
17976717-G-A 15864837-G-A CTS8396 Y+
18105030-G-C 15993150-G-C F22463 YY+
18115518-T-C 16003638-T-C MF1386 YY+
18577494-C-A 16465614-C-A FT301915 Y+
19000260-G-A 16888380-G-A FT302041 YY+
19157083-A-G 17045203-A-G CTS9935 YY+
21130645-T-A 18968759-T-A MF2645 YY+
21179892-C-A 19018006-C-A F23972 YY+
21331818-G-C 19169932-G-C F24171 YY+
21374276-G-T 19212390-G-T F24233 YY+
21593195-A-G 19431309-A-G F24481 YY+
21625529-C-T 19463643-C-T F24522 YY+
21692737-G-A 19530851-G-A F24590 YY+
21754361-A-G 19592475-A-G SK1721 YY+
21841239-A-G 19679353-A-G MF2646 Y+
22288095-A-G 20126209-A-G DYZ19 +
22466984-A-G 20305098-A-G DYZ19 +
22469887-T-C 20308001-T-C DYZ19 +
22472283-A-G 20310397-A-G DYZ19 +
22478024-C-G 20316138-C-G A762FGC28617 DYZ19 +
22483739-C-A 20321853-C-A FGC75614 DYZ19 +
22801761-C-A 20639875-C-A F25455 YY+
22851462-C-T 20689576-C-T FT302737 YY+
23101146-C-T 20939260-C-T Y+
23327205-A-G 21165319-A-G F25963 YY+
23491740-A-G 21329854-A-G F26140 YY+
23553833-G-C 21391947-G-C F26206 YY+
24444499-C-T 22298352-C-T F26647 Y+
28718927-G-A 26572780-G-A +
28794767-A-G 26648620-A-G +
58986588-T-C 56840441-T-C +

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.