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
NA18620
hg19:Y:5646236-G-T hg38:Y:5778195-G-T +
hg19:Y:2894082-C-T hg38:Y:3026041-C-T MF1811 FGC52922 YY+
hg19:Y:3242967-C-T hg38:Y:3374926-C-T FT316568 +
hg19:Y:3535385-T-G hg38:Y:3667344-T-G FT317586 +
hg19:Y:4068489-A-G hg38:Y:4200448-A-G FT319416 +
hg19:Y:4356362-A-G hg38:Y:4488321-A-G FT320380 +
hg19:Y:5201370-T-C hg38:Y:5333329-T-C FT323067 +
hg19:Y:5929265-G-A hg38:Y:6061224-G-A FT325532 +
hg19:Y:6104265-C-G hg38:Y:6236224-C-G F3735 +
hg19:Y:6542782-T-A hg38:Y:6674741-T-A FT326868 +
hg19:Y:6579653-A-T hg38:Y:6711612-A-T FT326888 +
hg19:Y:6609725-G-T hg38:Y:6741684-G-T +
hg19:Y:7590605-T-C hg38:Y:7722564-T-C FT300173 YY+
hg19:Y:7657118-C-T hg38:Y:7789077-C-T FT300195 YY+
hg19:Y:7800917-A-G hg38:Y:7932876-A-G F9966 YY+
hg19:Y:8156061-C-A hg38:Y:8288020-C-A FT300348 YY+
hg19:Y:8188189-C-T hg38:Y:8320148-C-T MF1813 YY+
hg19:Y:8198181-A-G hg38:Y:8330140-A-G FT300363 YY+
hg19:Y:8616847-G-T hg38:Y:8748806-G-T F3748 YY+
hg19:Y:8688684-G-T hg38:Y:8820643-G-T YY+
hg19:Y:8786136-G-A hg38:Y:8918095-G-A Y+
hg19:Y:9147244-C-A hg38:Y:9309635-C-A Y+
hg19:Y:9509614-T-A hg38:Y:9672005-T-A FT328066 +
hg19:Y:9763030-C-T hg38:Y:9925421-C-T F3759 Y+
hg19:Y:9809065-A-G hg38:Y:9971456-A-G FT300668 YY+
hg19:Y:9983853-A-C hg38:Y:10146244-A-C Y+
hg19:Y:13234698-G-T hg38:Y:11079022-G-T +
hg19:Y:13429369-C-A hg38:Y:11273693-C-A +
hg19:Y:13550526-T-A hg38:Y:11394850-T-A +
hg19:Y:13583711-C-T hg38:Y:11428035-C-T +
hg19:Y:13651548-C-T hg38:Y:11495872-C-T DYZ17 +
hg19:Y:13871648-G-T hg38:Y:11750942-G-T FT300688 Y+
hg19:Y:13936649-C-T hg38:Y:11815943-C-T PH722 Y+
hg19:Y:14041991-G-T hg38:Y:11921285-G-T FT300775 YY+
hg19:Y:14200590-T-A hg38:Y:12079884-T-A PH991 YY+
hg19:Y:14224027-C-A hg38:Y:12103321-C-A PH1022 YY+
hg19:Y:14484082-A-G hg38:Y:12363351-A-G PH1267 YY+
hg19:Y:14498652-C-G hg38:Y:12386857-C-G PH1275 YY+
hg19:Y:14504117-G-A hg38:Y:12392322-G-A PH1280 YY+
hg19:Y:14700160-C-A hg38:Y:12588226-C-A YY+
hg19:Y:14911296-A-G hg38:Y:12799363-A-G FT301033 YY+
hg19:Y:15021677-A-T hg38:Y:12909766-A-T PH1569 YY+
hg19:Y:15575372-A-T hg38:Y:13463492-A-T F1972 YY+
hg19:Y:16035325-A-G hg38:Y:13923445-A-G FT301312 Y+
hg19:Y:16343713-A-G hg38:Y:14231833-A-G F3778 YY+
hg19:Y:16500579-A-G hg38:Y:14388699-A-G Y+
hg19:Y:16645672-C-T hg38:Y:14533792-C-T FT301438 YY+
hg19:Y:16802482-A-C hg38:Y:14690602-A-C F3781 YY+
hg19:Y:16961375-T-C hg38:Y:14849495-T-C PH2723 YY+
hg19:Y:17053639-G-T hg38:Y:14941759-G-T PH2792 YY+
hg19:Y:17419016-T-G hg38:Y:15307136-T-G PH3055 YY+
hg19:Y:17624049-T-A hg38:Y:15512169-T-A PH3230 YY+
hg19:Y:17723728-G-A hg38:Y:15611848-G-A Y+
hg19:Y:17822864-A-C hg38:Y:15710984-A-C FT301739 Y+
hg19:Y:17869338-T-G hg38:Y:15757458-T-G PH3453 YY+
hg19:Y:17996680-G-A hg38:Y:15884800-G-A FT330672 P7_Gap Y+
hg19:Y:18419102-C-A hg38:Y:16307222-C-A FT301898 P6_Gap +
hg19:Y:18951313-G-T hg38:Y:16839433-G-T FT302022 YY+
hg19:Y:19009577-T-C hg38:Y:16897697-T-C FT302046 YY+
hg19:Y:19019956-G-A hg38:Y:16908076-G-A Y+
hg19:Y:19050869-C-G hg38:Y:16938989-C-G PH4179 YY+
hg19:Y:21111641-G-T hg38:Y:18949755-G-T FT302237 YY+
hg19:Y:21141736-T-C hg38:Y:18979850-T-C PH4668 YY+
hg19:Y:21207295-G-A hg38:Y:19045409-G-A FT302261 Y+
hg19:Y:21368093-G-A hg38:Y:19206207-G-A PH4788 YY+
hg19:Y:21423003-T-A hg38:Y:19261117-T-A F3806 YY+
hg19:Y:21485962-C-A hg38:Y:19324076-C-A FT302389 YY+
hg19:Y:21540432-C-T hg38:Y:19378546-C-T Y+
hg19:Y:21933586-C-T hg38:Y:19771700-C-T PH5034 YY+
hg19:Y:22229988-G-C hg38:Y:20068102-G-C DYZ19 +
hg19:Y:22320042-A-C hg38:Y:20158156-A-C DYZ19 +
hg19:Y:22477532-A-C hg38:Y:20315646-A-C DYZ19 +
hg19:Y:22478446-G-C hg38:Y:20316560-G-C BY50933 DYZ19 +
hg19:Y:22681457-A-G hg38:Y:20519571-A-G PH5176 YY+
hg19:Y:22824445-G-T hg38:Y:20662559-G-T FT302729 YY+
hg19:Y:23306866-G-T hg38:Y:21144980-G-T FT302859 YY+
hg19:Y:23327292-A-T hg38:Y:21165406-A-T FT302864 YY+
hg19:Y:23568363-G-A hg38:Y:21406477-G-A F3813 YY+
hg19:Y:28503015-A-G hg38:Y:26356868-A-G FT303078 +
hg19:Y:28586729-A-T hg38:Y:26440582-A-T FT44565 +
hg19:Y:28737770-T-C hg38:Y:26591623-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.




Big Tree Main Page