Tree Position

R-P312/S116 > Z40481 > ZZ11 > U152/S28 > L2/S139 > Z367/S255 > L20/S144 > Z1909

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 STRFTDNA
15371775-A-G 13259895-A-G BY101166 YY+
15749823-G-A 13637943-G-A BY103812 YY+
8998754-G-A 9161145-G-A BY77162 Y+
9149514-G-A 9311905-G-A BY78558 Y+
21594164-G-C 19432278-G-C BY134055 YY+
21519961-C-G 19358075-C-G BY133572 YY+
21138035-TA-T 18976149-TA-T +
13863898-A-G 11743192-A-G BY91610 +
14437465-A-G 12316738-A-G BY95763 Y+
15015213-A-G 12903301-A-G BY99104 YY+
16238369-A-C 14126489-A-C BY106242 YY+
19313497-G-C 17201617-G-C BY128166 YY+
16369287-G-C 14257407-G-C BY107288 YY+
16449124-T-C 14337244-T-C BY107884 YY+
16751603-C-T 14639723-C-T Y97179 YY+
19314351-G-A 17202471-G-A BY128174 YY+
16951199-G-T 14839319-G-T BY156613 YY+
17129927-C-T 15018047-C-T BY112505 YY+
17529854-C-T 15417974-C-T BY115499 YY+
18264490-G-A 16152610-G-A BY121300 +
19191822-T-A 17079942-T-A BY127096 YY+
8612460-G-A 8744419-G-A BY74545 YY+
8436740-G-A 8568699-G-A BY72739 FT60002 YY+
7690352-A-G 7822311-A-G BY66936 YY+
22457733-G-T 20295847-G-T BY43875 DYZ19 +
23531195-A-G 21369309-A-G BY145981 YY+
23396794-T-C 21234908-T-C BY145027 YY+
22770571-G-A 20608685-G-A Y131606 YY+
6635812-T-C 6767771-T-C BY60446 YY+
22459263-A-G 20297377-A-G BY21587BY21587 DYZ19 +
19238922-T-G 17127042-T-G BY127582 YY+
2910901-G-A 3042860-G-A BY57255 YY+
22369251-G-T 20207365-G-T DYZ19 **
7898045-A-G 8030004-A-G PF3864 **
14850651-C-T 12738717-C-T PR1577 **
19417241-A-G 17305361-A-G CTS10348 **
15718966-C-A 13607086-C-A CTS4569 **
13294290-T-A 11138614-T-A **
22511714-T-C 20349828-T-C DYZ19 ***
22241178-G-C 20079292-G-C DYZ19 ***
22292816-C-A 20130930-C-A DYZ19 ***
22232966-C-A 20071080-C-A DYZ19 ***
22489858-T-G 20327972-T-G DYZ19 ***
22249530-T-C 20087644-T-C DYZ19 ***
25130008-C-T 22983861-C-T g1 ***
25220531-G-A 23074384-G-A P2_r1 ***
25248818-G-A 23102671-G-A P2_r1 ***
19865445-T-A 17753565-T-A P5_Prx ***
13659417-G-T 11503741-G-T ***
16937296-G-GTCTCTCTTCC 14825416-G-GTCTCTCTTCC ***
58979010-C-T 56832863-C-T ***
22367899-G-A 20206013-G-A DYZ19 ***
13852205-T-A 11731499-T-A ***
22367847-G-C 20205961-G-C DYZ19 ***
28784668-T-A 26638521-T-A FT461730 ***
13458932-G-GTTCCA 11303256-G-GTTCCA 5×TTCCA***
13700958-T-G 11545282-T-G 5×GAATG***
58979031-C-T 56832884-C-T ***
22364046-G-T 20202160-G-T DYZ19 ***
13543631-C-A 11387955-C-A ***
13677847-T-A 11522171-T-A ***
13476420-A-C 11320744-A-C ***
13659436-G-T 11503760-G-T ***
6346345-C-CAT 6478304-C-CAT 10×AT***
13659431-G-A 11503755-G-A ***
13659415-T-A 11503739-T-A ***
13700953-G-T 11545277-G-T ***
13814009-GT-G 11693303-GT-G ***
26152372-T-C 24006225-T-C P1_Y1 ***

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.

Age Analysis Information (work in progress)

Kit: B864451015423772669107330402
Used in age calculations1015423772669107330402
Counts of SNPs2526
Variant counts last updated 2022-07-25 03:21:15.

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