Tree Position

A0-T-YP2191 > P305[A1] > A1b > BT/A1b2 > M168/PF1416[CT] > P143[CF] > M130[C]

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.

Position Blocks Names Region McDonald BED combBED STR1kG
NA18612
hg19:Y:14313081-C-T hg38:Y:12192375-C-T A2121CTS2457 YY+
hg19:Y:13416135-T-G hg38:Y:11260459-T-G +
hg19:Y:2815306-G-C hg38:Y:2947265-G-C Z31672 YY+
hg19:Y:3009582-G-A hg38:Y:3141541-G-A FT315733 +
hg19:Y:3059685-A-G hg38:Y:3191644-A-G FGC45568 +
hg19:Y:3540914-G-A hg38:Y:3672873-G-A FT317610 +
hg19:Y:3609603-T-C hg38:Y:3741562-T-C FGC45561 +
hg19:Y:3872309-C-T hg38:Y:4004268-C-T FT318796 +
hg19:Y:3883696-C-T hg38:Y:4015655-C-T FT95187 +
hg19:Y:3999349-T-C hg38:Y:4131308-T-C FT319194 +
hg19:Y:4366009-G-A hg38:Y:4497968-G-A FGC45556 +
hg19:Y:4551756-A-G hg38:Y:4683715-A-G FGC45544 +
hg19:Y:4565852-C-T hg38:Y:4697811-C-T Z31673 F9086 +
hg19:Y:5340973-A-G hg38:Y:5472932-A-G FGC45547 +
hg19:Y:7056501-C-T hg38:Y:7188460-C-T PH404 YY+
hg19:Y:7739238-G-A hg38:Y:7871197-G-A FGC45551 YY+
hg19:Y:7742460-G-T hg38:Y:7874419-G-T Z31674 F9951 YY+
hg19:Y:7961051-C-A hg38:Y:8093010-C-A Z31675 F10004 YY+
hg19:Y:8131816-T-C hg38:Y:8263775-T-C FGC45548 YY+
hg19:Y:8316802-T-G hg38:Y:8448761-T-G FT300397 YY+
hg19:Y:8316855-A-G hg38:Y:8448814-A-G FT300398 YY+
hg19:Y:8399738-C-A hg38:Y:8531697-C-A Z31669 YY+
hg19:Y:8507204-C-G hg38:Y:8639163-C-G FT300461 YY+
hg19:Y:8540770-G-C hg38:Y:8672729-G-C FT300472 YY+
hg19:Y:8545183-C-T hg38:Y:8677142-C-T Z31676 F10136 YY+
hg19:Y:9021478-G-A hg38:Y:9183869-G-A FT300599 Y+
hg19:Y:9051877-C-G hg38:Y:9214268-C-G MF1629 Y35925 Z45207 Y+
hg19:Y:10011813-A-G hg38:Y:10174204-A-G FGC45555 Y+
hg19:Y:10020315-G-A hg38:Y:10182706-G-A FGC45558 Y+
hg19:Y:10052097-T-A hg38:Y:10214488-T-A +
hg19:Y:13131207-C-G hg38:Y:10620693-C-G +
hg19:Y:13201672-C-T hg38:Y:11045996-C-T +
hg19:Y:13515793-C-T hg38:Y:11360117-C-T +
hg19:Y:13628986-G-T hg38:Y:11473310-G-T FGC45550 +
hg19:Y:13948557-T-C hg38:Y:11827851-T-C PH734 Y+
hg19:Y:13982190-G-T hg38:Y:11861484-G-T S3181 F11263 Y+
hg19:Y:14312438-C-T hg38:Y:12191732-C-T PH1109 YY+
hg19:Y:14372243-T-A hg38:Y:12251539-T-A FT300908 YY+
hg19:Y:14372244-C-T hg38:Y:12251540-C-T YY+
hg19:Y:14504003-G-A hg38:Y:12392208-G-A PH1279 YY+
hg19:Y:14623043-C-G hg38:Y:12511241-C-G FGC45565 YY+
hg19:Y:14717968-G-T hg38:Y:12606036-G-T FT300993 Y+
hg19:Y:14734460-A-G hg38:Y:12622528-A-G FGC45562 YY+
hg19:Y:14884838-C-G hg38:Y:12772904-C-G CTS3385 YY+
hg19:Y:14886238-T-C hg38:Y:12774304-T-C FT301028 YY+
hg19:Y:15842210-G-A hg38:Y:13730330-G-A PH1845 YY+
hg19:Y:15940435-T-G hg38:Y:13828555-T-G PH1906 YY+
hg19:Y:16244709-G-T hg38:Y:14132829-G-T PH2109 YY+
hg19:Y:16282232-C-T hg38:Y:14170352-C-T Z31677 YY+
hg19:Y:16337272-T-A hg38:Y:14225392-T-A PH2194 YY+
hg19:Y:16784372-G-A hg38:Y:14672492-G-A FT301479 YY+
hg19:Y:16997207-T-C hg38:Y:14885327-T-C FT301520 Y+
hg19:Y:17740686-C-A hg38:Y:15628806-C-A Y+
hg19:Y:17876434-G-C hg38:Y:15764554-G-C FT301761 YY+
hg19:Y:17945116-G-T hg38:Y:15833236-G-T FT301783 YY+
hg19:Y:18048587-C-A hg38:Y:15936707-C-A PH3634 YY+
hg19:Y:18060147-C-T hg38:Y:15948267-C-T Z31678 F12408 YY+
hg19:Y:18103043-T-C hg38:Y:15991163-T-C PH3692 F12415 YY+
hg19:Y:18713612-C-T hg38:Y:16601732-C-T PH3947 F12528 YY+
hg19:Y:18943811-G-T hg38:Y:16831931-G-T Z31679 F12583 YY+
hg19:Y:19004342-G-A hg38:Y:16892462-G-A PH4151 YY+
hg19:Y:19005805-T-A hg38:Y:16893925-T-A FT302045 YY+
hg19:Y:19263894-G-C hg38:Y:17152014-G-C FGC45564 YY+
hg19:Y:19264026-A-C hg38:Y:17152146-A-C CTS10112 YY+
hg19:Y:19402962-T-C hg38:Y:17291082-T-C PH4484 YY+
hg19:Y:20804906-T-C hg38:Y:18643020-T-C FT302205 P4_Gap +
hg19:Y:20808486-T-C hg38:Y:18646600-T-C FT302207 P4_Gap +
hg19:Y:21353808-A-G hg38:Y:19191922-A-G PH4779 F12881 YY+
hg19:Y:21421383-T-A hg38:Y:19259497-T-A FT302360 Y+
hg19:Y:21509635-A-C hg38:Y:19347749-A-C FT302398 YY+
hg19:Y:21672900-C-G hg38:Y:19511014-C-G FT302445 YY+
hg19:Y:21893184-T-G hg38:Y:19731298-T-G PH5006 F13062 YY+
hg19:Y:22091718-A-G hg38:Y:19929832-A-G Z31680 F13141 YY+
hg19:Y:22244133-G-C hg38:Y:20082247-G-C DYZ19 +
hg19:Y:22257503-C-T hg38:Y:20095617-C-T FGC81531 DYZ19 +
hg19:Y:22316516-C-A hg38:Y:20154630-C-A DYZ19 +
hg19:Y:22316521-A-G hg38:Y:20154635-A-G DYZ19 +
hg19:Y:22316799-G-T hg38:Y:20154913-G-T BY217229 DYZ19 +
hg19:Y:22316978-G-C hg38:Y:20155092-G-C DYZ19 +
hg19:Y:22445388-G-A hg38:Y:20283502-G-A FT456999 DYZ19 +
hg19:Y:22462835-C-A hg38:Y:20300949-C-A FT458069 DYZ19 +
hg19:Y:22473332-T-C hg38:Y:20311446-T-C DYZ19 +
hg19:Y:22507143-G-C hg38:Y:20345257-G-C BY225321 DYZ19 +
hg19:Y:22509354-G-T hg38:Y:20347468-G-T DYZ19 +
hg19:Y:22611496-G-A hg38:Y:20449610-G-A BY171331 YY+
hg19:Y:22874654-G-A hg38:Y:20712768-G-A CTS10989 YY+
hg19:Y:22967707-G-A hg38:Y:20805821-G-A FT182573 YY+
hg19:Y:22996177-T-C hg38:Y:20834291-T-C FGC45559 YY+
hg19:Y:23382400-G-A hg38:Y:21220514-G-A FGC45569 YY+
hg19:Y:23386847-G-T hg38:Y:21224961-G-T FT302883 YY+
hg19:Y:23734799-C-T hg38:Y:21572913-C-T Z31681 +
hg19:Y:28551345-C-T hg38:Y:26405198-C-T FGC45567 +
hg19:Y:28694535-A-G hg38:Y:26548388-A-G Z31682 F14003 +
hg19:Y:28727674-G-A hg38:Y:26581527-G-A FGC45546 Y+
hg19:Y:28768557-C-T hg38:Y:26622410-C-T F14035 FGC45543 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.




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