Tree Position

R-P312/S116 > Z40481 > ZZ11 > DF27/S250 > ZZ12 > Z46512 > FGC20747 > Z1899 > CTS1643 > Y4865

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
19448250-G-A 17336370-G-A PF7596 YY+
18102300-C-A 15990420-C-A Y101297 YY+
16766215-C-T 14654335-C-T Y97230 YY+
17370274-T-A 15258394-T-A Y98959 YY+
22485239-G-C 20323353-G-C DYZ19 +
17612455-T-C 15500575-T-C Y99718 YY+
17680361-A-G 15568481-A-G Y99915 YY+
17879740-G-C 15767860-G-C Y100499 YY+
17956536-A-C 15844656-A-C Y100769 YY+
18205649-C-T 16093769-C-T Y101633 YY+
15874251-G-C 13762371-G-C Y95013 YY+
24367777-C-T 22221630-C-T Y112688 +
21252566-A-C 19090680-A-C Y105853 YY+
21373238-T-G 19211352-T-G Y106277 YY+
21623147-A-G 19461261-A-G Y107058 YY+
22242884-C-A 20080998-C-A DYZ19 +
23886996-T-G 21725110-T-G Y+
22475724-G-T 20313838-G-T DYZ19 +
23474695-T-C 21312809-T-C Y111639 YY+
16697211-G-C 14585331-G-C Y97057 YY+
22485231-G-A 20323345-G-A DYZ19 +
15351376-C-T 13239495-C-T Y93608 YY+
9837729-CA-C 10000120-CA-C +
7977055-A-T 8109014-A-T Y85516 YY+
15306201-A-G 13194303-A-G Y93465 YY+
23954804-C-T 21808657-C-T Z26010 F14685 +
22468771-T-A 20306885-T-A BY222117 DYZ19 +
9516029-C-G 9678420-C-G BY80077 +
9519092-G-C 9681483-G-C BY80125 +
8081136-G-A 8213095-G-A Y85788 YY+
8109052-C-A 8241011-C-A Y85856 YY+
13703496-G-T 11547820-G-T BY89078 +
14288859-C-T 12168153-C-T Y90947 YY+
14789123-G-A 12677194-G-A Y92205 YY+
14834604-T-C 12722671-T-C Y92312 YY+
22484767-G-C 20322881-G-C DYZ19 **
22484783-G-A 20322897-G-A DYZ19 **
17466749-T-C 15354869-T-C PR2484 **
22484793-A-C 20322907-A-C DYZ19 **
22475730-A-G 20313844-A-G DYZ19 **
17448818-G-A 15336938-G-A Y99186 **
13919315-G-A 11798609-G-A Y89872 **
17448819-C-A 15336939-C-A Y99187 **
24351811-T-C 22205664-T-C P3_t1 ***
26901595-G-A 24755448-G-A P1_r3 ***
24992195-TA-T 22846048-TA-T g1 ***
24085108-A-G 21938961-A-G P3_b1 ***
25007308-A-G 22861161-A-G g1 ***
25007322-A-T 22861175-A-T g1 ***
26228692-T-TC 24082545-T-TC P1_Y1 ***
27321327-T-A 25175180-T-A P1_g3 ***
25180943-T-G 23034796-T-G g1 ***
24969132-AT-A 22822985-AT-A g1 ***
28796128-A-G 26649981-A-G ***
22475786-A-T 20313900-A-T DYZ19 ***
22423363-G-C 20261477-G-C DYZ19 ***
22315914-G-A 20154028-G-A DYZ19 ***
20711076-T-C 18549190-T-C P4_Prx ***
19925923-T-C 17814043-T-C P5_Prx ***
19913015-G-C 17801135-G-C P5_Prx ***
19781008-G-T 17669128-G-T P5_Prx ***
19781002-CA-C 17669122-CA-C P5_Prx ***
22475800-C-G 20313914-C-G BY196887 DYZ19 ***
17108837-T-TGCACATCAC 14996957-T-TGCACATCAC ***
10017431-G-A 10179822-G-A ***
9193041-G-A 9355432-G-A ***
22475820-T-A 20313934-T-A BY39770BY42454 DYZ19 ***
27321341-T-C 25175194-T-C P1_g3 ***

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: 5599891079754778530517944397
Used in age calculations1079754778530517944397
Counts of SNPs2324
Variant counts last updated 2020-09-22 02:41:33.

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