Tree Position

R-P312/S116 > Z40481 > ZZ11 > U152/S28 > L2/S139 > Z41150 > BY4245 > BY3504 > 15984654-CAT-C > BY3478 > BY14173 > Y100302

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
E4959
BigY3
E4959
26484790-T-TTTTA 24338643-T-TTTTA P1_Y1 6×TTTAA*
5548462-A-T 5680421-A-T A*
58987677-G-A 56841530-G-A A*
59014246-C-G 56868099-C-G A*
6193870-A-G 6325829-A-G IR3_Dst ***A*
19864596-T-C 17752716-T-C P5_Prx ***A*
16217389-A-AT 14105509-A-AT 10×TA*
56841705-T-C A*
13477293-G-T 11321617-G-T A*
20368135-C-A 18206249-C-A P5_Dst A*
13470197-A-T 11314521-A-T A*
56826117-C-A A*
13472133-A-C 11316457-A-C A*
16110965-C-A 13999085-C-A P8_Prx A*
18350018-A-G 16238138-A-G P6_Prx A*
19607681-T-C 17495801-T-C P5_Prx YA*
19636179-C-T 17524299-C-T P5_Prx A*
19653399-A-G 17541519-A-G P5_Prx A*
10004883-G-A 10167274-G-A Y+
21309685-G-A 19147799-G-A FGC52204 YY++
2714848-T-C 2846807-T-C Y81276 YY++
3544897-C-T 3676856-C-T Y81871 **+
6428335-C-A 6560294-C-A BY46446 ++
6931033-C-G 7062992-C-G Z36300 YY++
6960690-T-TC 7092649-T-TC ++
7694878-G-A 7826837-G-A Y84694 YY++
8768956-A-G 8900915-A-G Y87951 YY++
9107740-C-T 9270131-C-T Y88603 Y++
16373999-C-T 14262119-C-T Y96144 YY++
17809842-G-A 15697962-G-A Y100297 YY++
17893080-T-C 15781200-T-C Y100551 YY++
19215353-A-G 17103473-A-G Y104028 YY++
19228190-A-T 17116310-A-T Y104074 YY++
21283894-G-A 19122008-G-A Y105947 YY++
22002941-A-G 19841055-A-G Y108111 YY++
22272584-T-C 20110698-T-C BY215417 DYZ19 +**
22419762-C-G 20257876-C-G BY217727 DYZ19 +
22610750-GA-G 20448864-GA-G 9×A++
22632434-C-T 20470548-C-T Y109335 Y++
22684740-A-C 20522854-A-C Y109464 YY++
23235906-C-G 21074020-C-G Y111029 Y++
23587497-A-C 21425611-A-C BY146522 YY++
22562391-G-A 20400505-G-A Y109093 YY+
3818248-TTAAC-T 3950207-TTAAC-T +
3925911-T-C 4057870-T-C +
4348360-T-C 4480319-T-C +
4492276-A-G 4624235-A-G +
18753196-G-A 16641316-G-A Y+
19393279-T-C 17281399-T-C YY+
23253228-C-T 21091342-C-T YY+
22312540-G-T 20150654-G-T DYZ19 ****
22312541-G-T 20150655-G-T DYZ19 ****
13450192-C-T 11294516-C-T *
13446042-T-A 11290366-T-A **
22099633-TTTATTATTA-T 19937747-TTTATTATTA-T 16×TTA*****
13811898-G-A 11691192-G-A ****
10654572-T-C **
10973960-C-A **
25934375-T-TAA 23788228-T-TAA P1_Y1 17×A**
15264740-G-T 13152829-G-T YP4120 **
13461794-G-A 11306118-G-A **
13453344-C-CTTG 11297668-C-CTTG **
8181175-ATTTTTTTTTTTTTTTTTTTTTT-A 8313134-ATTTTTTTTTTTTTTTTTTTTTT-A 38×T**
25520340-C-CT 23374193-C-CT P1_gr1 16×T**
19788371-C-A 17676491-C-A P5_Prx **
4279738-T-TTG 4411697-T-TTG 10×TG**
22457489-G-T 20295603-G-T DYZ19 **
22346396-A-G 20184510-A-G DYZ19 **
4288482-C-A 4420441-C-A **
5572565-G-A 5704524-G-A **
10654549-C-T **
10654580-AT-A **
10654585-A-AG **
19676594-A-C 17564714-A-C P5_Prx **
19764651-A-C 17652771-A-C P5_Prx **
19782515-T-G 17670635-T-G P5_Prx **
19795511-T-A 17683631-T-A P5_Prx **
22345660-A-G 20183774-A-G DYZ19 **
26053817-C-A 23907670-C-A P1_Y1 **
26311433-T-G 24165286-T-G P1_Y1 **
13696552-A-C 11540876-A-C ***
25208330-TAA-T 23062183-TAA-T P2_r1 17×A***
5471896-AAAAGAAAGAAAGAAAGAAAG-A 5603855-AAAAGAAAGAAAGAAAGAAAG-A 17×AAAG***
13674765-ATTT-A 11519089-ATTT-A ***
13838485-AGGAATGGAAT-A 11717779-AGGAATGGAAT-A 9×GGAAT***
17086601-TCATA-T 14974721-TCATA-T ***
22449287-G-A 20287401-G-A DYZ19 ***
5240956-T-TTCCC 5372915-T-TTCCC 5×TCCC***
13452080-T-C 11296404-T-C ***
9344615-T-C 9507006-T-C ***
22264983-T-C 20103097-T-C DYZ19 ***
22299927-C-G 20138041-C-G DYZ19 ******
23692967-T-C 21531081-T-C ***
58968940-C-A 56822793-C-A ***
58979543-A-T 56833396-A-T ***
17685339-C-CT 15573459-C-CT 10×T***
13468261-C-A 11312585-C-A ***
10987174-T-C ***
3341780-GT-G 3473739-GT-G 11×T***
13818091-AC-A 11697385-AC-A ***
14926462-CAAA-C 12814527-CAAA-C 26×A***
17997640-C-A 15885760-C-A P7_Gap ***
10872200-G-T ***
13468315-CC-G 11312639-CC-G ***
10691347-CATTCCATTCCATTCCATTCCATTCCA-C,CTTTCCTTTCCATTCCATTCCATTTCA ***
13450305-ATTCCATTGCATTTAA-A,ATTCCATTGCATTTCC 11294629-ATTCCATTGCATTTAA-A,ATTCCATTGCATTTCC ***
4277201-CT-C,CTT 4409160-CT-C,CTT 20×T***
13267431-CAA-C,CA 11111755-CAA-C,CA 16×A***
13486189-T-C 11330513-T-C ***
13486190-A-C 11330514-A-C ***
13486212-G-T 11330536-G-T ***
13486213-T-C 11330537-T-C ***
13486231-T-C 11330555-T-C ***
17622744-T-A 15510864-T-A ***
22346401-T-C 20184515-T-C DYZ19 ***
4650471-TGA-T 4782430-TGA-T ***
5387463-C-A 5519422-C-A ***
5453486-G-T 5585445-G-T ***
7107011-CTATA-C,CTA 7238970-CTATA-C,CTA 20×TA***
10747202-T-C ***
10903694-G-A ***
10927637-T-C ***
21084329-ATATA-A,ATATG 18922443-ATATA-A,ATATG ***
22345653-C-A 20183767-C-A DYZ19 ***
22345659-C-A 20183773-C-A DYZ19 ***
22457488-T-G 20295602-T-G DYZ19 ***

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.