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
NA18635
16654726-C-T 14542846-C-T CTS6078 YY+
15324003-A-G 13212121-A-G MF1491 YY+
2712735-G-A 2844694-G-A CTS75 YY+
2908668-T-C 3040627-T-C MF1478 YY+
3105004-A-G 3236963-A-G FT316092 +
3565553-T-C 3697512-T-C FT317758 +
3608284-C-T 3740243-C-T FT317899 +
4199811-A-G 4331770-A-G FT319862 +
4351956-G-T 4483915-G-T +
4742556-T-C 4874515-T-C +
4889332-G-C 5021291-G-C FT322024 +
4893625-A-G 5025584-A-G FT322043 +
5087364-C-A 5219323-C-A FT322676 +
5232312-A-G 5364271-A-G FT323178 +
5695698-A-G 5827657-A-G FT324801 +
5758897-G-A 5890856-G-A +
5834255-A-G 5966214-A-G FT325208 +
6347169-T-G 6479128-T-G FT326274 +
6436082-C-T 6568041-C-T FT71758 +
6445775-A-G 6577734-A-G FT326571 +
6484560-A-G 6616519-A-G FT326709 +
6495825-G-A 6627784-G-A +
6704379-G-C 6836338-G-C PH147 YY+
6845358-A-G 6977317-A-G PH233 YY+
7172286-A-C 7304245-A-C PH483 YY+
7299902-G-A 7431861-G-A FT300108 Y+
7921936-C-T 8053895-C-T YY+
8072434-A-G 8204393-A-G F16610 YY+
8541490-T-C 8673449-T-C F17209 YY+
8744081-C-T 8876040-C-T F17439 YY+
8820767-A-G 8952726-A-G F17518 YY+
8900741-C-T 9032700-C-T MF1483 Y+
8911657-G-A 9043616-G-A MF1484 +
9009637-T-A 9172028-T-A MF1485 Y+
9164120-G-A 9326511-G-A +
9453943-C-T 9616334-C-T FT300665 YY+
9516330-C-T 9678721-C-T FT328090 +
9807737-C-T 9970128-C-T F17923 YY+
9832511-A-T 9994902-A-T Y19706 YY+
13211782-G-C 11056106-G-C MF1488 +
13221591-C-T 11065915-C-T MF1489 +
13225511-C-A 11069835-C-A FT441259 8×A+
13298720-G-A 11143044-G-A +
13647749-T-G 11492073-T-G +
13700529-C-G 11544853-C-G +
13801810-G-A 11681104-G-A MF1490 +
13862434-G-A 11741728-G-A FT328836 +
14003977-G-A 11883271-G-A CTS1646 YY+
14059197-C-T 11938491-C-T FT300786 YY+
14060992-T-A 11940286-T-A PH851 YY+
14078107-T-G 11957401-T-G CTS1811 YY+
14305452-G-C 12184746-G-C FT300880 Y+
14458319-C-T 12337592-C-T YY+
14587748-C-T 12475948-C-T YY+
14591266-C-T 12479466-C-T PH1353 YY+
14712907-C-T 12600974-C-T CTS3189 YY+
15031874-G-A 12919962-G-A PH1581 YY+
15053793-A-T 12941884-A-T PH1600 YY+
15090476-A-G 12978565-A-G F19550 YY+
15287436-C-T 13175535-C-T FT301124 Y+
15407273-C-G 13295393-C-G CTS4119 YY+
15556230-A-C 13444350-A-C F19910 YY+
16068941-A-G 13957061-A-G CTS5217 Y+
16326110-A-G 14214230-A-G CTS5505 YY+
16506532-C-G 14394652-C-G MF1492 YY+
16603986-A-G 14492106-A-G PH2397 YY+
16684759-C-T 14572879-C-T CTS6123 Y+
16729240-G-A 14617360-G-A CTS6206 YY+
16768705-T-C 14656825-T-C PH2504 YY+
17017023-C-T 14905143-C-T MF1493 YY+
17069338-A-G 14957458-A-G FT301543 Y+
17073893-G-A 14962013-G-A PH2807 YY+
17224112-C-T 15112232-C-T CTS6988 YY+
17679912-A-T 15568032-A-T PH3281 YY+
17746964-G-A 15635084-G-A PH3338 YY+
17818019-C-T 15706139-C-T CTS8059 YY+
17964970-A-C 15853090-A-C FT301788 Y+
18382266-G-A 16270386-G-A MF1495 P6_Gap +
18601846-A-C 16489966-A-C F22711 YY+
18623304-T-G 16511424-T-G FT301926 Y+
18849114-A-G 16737234-A-G FT301985 Y+
19079803-T-C 16967923-T-C PH4195 YY+
19142356-G-T 17030476-G-T PH4267 YY+
19145232-C-G 17033352-C-G PH4272 YY+
19231520-G-A 17119640-G-A PH4360 YY+
19249568-A-T 17137688-A-T CTS10092 Y+
19315552-A-G 17203672-A-G F23570 YY+
19345750-T-C 17233870-T-C PH4442 YY+
19445466-T-C 17333586-T-C PH4509 YY+
19464468-A-T 17352588-A-T CTS10458 Y+
21057439-C-T 18895553-C-T Y+
21203204-C-G 19041318-C-G F23996 YY+
21284753-A-G 19122867-A-G MF1498 YY+
21295004-G-A 19133118-G-A F24104 YY+
21368475-G-T 19206589-G-T PH4789 YY+
21445620-T-A 19283734-T-A MF1500 YY+
21539779-G-C 19377893-G-C Y+
21551908-T-C 19390022-T-C FT302408 Y+
21783610-C-A 19621724-C-A MF1501 YY+
21915335-T-G 19753449-T-G Y+
22007624-G-A 19845738-G-A F24924 YY+
22025406-A-G 19863520-A-G F24938 YY+
22219320-T-C 20057434-T-C DYZ19 +
22260106-G-T 20098220-G-T DYZ19 +
22272390-C-A 20110504-C-A DYZ19 +
22464070-G-A 20302184-G-A DYZ19 +
22468358-G-T 20306472-G-T DYZ19 +
22476001-T-A 20314115-T-A DYZ19 +
22476340-G-A 20314454-G-A DYZ19 +
22479464-T-A 20317578-T-A DYZ19 +
22483434-T-G 20321548-T-G DYZ19 +
22485340-G-A 20323454-G-A DYZ19 +
22613674-G-T 20451788-G-T F25307 YY+
22711089-G-A 20549203-G-A F25382 YY+
22916033-C-A 20754147-C-A CTS11045 YY+
23030815-G-A 20868929-G-A PH5310 YY+
23191902-G-T 21030016-G-T PH5347 Y+
23446815-G-A 21284929-G-A CTS12053 YY+
23486143-T-A 21324257-T-A F26134 YY+
23523150-C-A 21361264-C-A F26165 YY+
23631201-G-A 21469315-G-A F26314 YY+
28514636-C-T 26368489-C-T F26728 Y+
28766553-T-G 26620406-T-G CTS12965 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.