Tree Position

R-P312/S116 > Z290 > L21/S145 > S552 > DF13 > Z39589 > FGC20101

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 STRBigY3
3201688-A-G 3333647-A-G A*
24302115-C-T 22155968-C-T P3_t1 A*
20668654-C-T 18506768-C-T P4_Prx A*
6236873-C-G 6368832-C-G IR3_Dst A*
19636033-G-A 17524153-G-A P5_Prx A*
19792163-A-G 17680283-A-G P5_Prx A*
19891071-T-G 17779191-T-G P5_Prx A*
20700035-T-C 18538149-T-C P4_Prx A*
26130746-C-T 23984599-C-T P1_Y1 A*
26136450-T-C 23990303-T-C P1_Y1 A*
28817427-T-TG 26671280-T-TG A*
13458551-G-A 11302875-G-A BY85533 +
14233129-T-A 12112423-T-A 6102647-G-AA7649 YY+
22420057-C-T 20258171-C-T BY217784 DYZ19 +
10655297-A-C FGC77405 +
4875456-G-T 5007415-G-T FT235468 +
17679167-T-A 15567287-T-A FT237233 YY11×A+
3019990-C-A 3151949-C-A FT234967 +
3338403-A-G 3470362-A-G FT235065 +
3367705-C-T 3499664-C-T FT235079 +
3919681-C-A 4051640-C-A FT235230 +
4034475-G-A 4166434-G-A FT235254 +
4083674-A-G 4215633-A-G FT235263 +
4119072-T-C 4251031-T-C FT235276 +
4408865-C-CA 4540824-C-CA +
4590731-C-G 4722690-C-G FT235393 +
4749322-TATC-T 4881281-TATC-T +
5010840-A-T 5142799-A-T FT235496 +
5413572-C-A 5545531-C-A FT235593 +
6598691-C-A 6730650-C-A FT235834 +
6942394-T-G 7074353-T-G FT235902 YY+
7335709-C-T 7467668-C-T FT235969 YY+
7373156-C-T 7505115-C-T FT235976 Y+
7903048-C-T 8035007-C-T FT236075 YY+
8067613-A-G 8199572-A-G FT167609 YY+
8465853-C-G 8597812-C-G YY+
10057319-G-T 10219710-G-T FT359100 +
10687800-C-T FT359098 +
11654244-G-T FT450430 +
13831248-T-C 11710542-T-C BY7211 +
14116847-CT-C 11996141-CT-C +
14715812-G-A 12603879-G-A FT236648 Y+
14860855-C-T 12748921-C-T FT236673 YY+
14899939-G-A 12788006-G-A FT236682 YY+
15621502-C-T 13509622-C-T FT236818 YY+
16347542-T-C 14235662-T-C FT236929 YY+
16819343-T-G 14707463-T-G FT237032 YY+
17122265-G-A 15010385-G-A FT237088 YY+
17448513-G-T 15336633-G-T FT237172 YY+
18223176-T-C 16111296-T-C FT237356 Y+
18682424-C-T 16570544-C-T FT68532 YY+
18724147-G-A 16612267-G-A FT237413 YY+
18884919-T-C 16773039-T-C FT237449 YY+
19225387-T-C 17113507-T-C FT237523 YY+
19269935-A-C 17158055-A-C FT237536 YY+
19392213-T-C 17280333-T-C FT237561 YY+
19466422-C-A 17354542-C-A FT237575 YY+
21172987-C-A 19011101-C-A FT237619 YY+
21320423-G-T 19158537-G-T FT237648 Y+
21481901-G-A 19320015-G-A FT237699 YY+
21817094-G-A 19655208-G-A FT237768 YY+
22270377-T-A 20108491-T-A FT359099 DYZ19 +
22951273-A-G 20789387-A-G FT237957 YY+
24604539-C-G 22458392-C-G FT460976 P3_t2 +
26328734-A-T 24182587-A-T P1_Y1 +
10668622-GTTCCATTCCA-G *
10769883-T-TTCCAC *
22275163-A-T 20113277-A-T DYZ19 *
22278715-T-TAA 20116829-T-TAA DYZ19 *
22278749-T-C 20116863-T-C DYZ19 *
20758657-G-T 18596771-G-T P4_Prx **
6523223-C-T 6655182-C-T A15932 **
14181302-C-CA 12060596-C-CA **
27297696-G-A 25151549-G-A P1_g3 **
7613952-C-T 7745911-C-T **
13457370-T-C 11301694-T-C **
13457380-T-C 11301704-T-C **
2791788-A-G 2923747-A-G **
3118880-A-G 3250839-A-G **
5963932-A-T 6095891-A-T **
6008930-G-A 6140889-G-A **
13387840-G-A 11232164-G-A **
13557318-A-G 11401642-A-G **
15235352-C-T 13123438-C-T **
15644764-T-C 13532884-T-C **
15690027-A-T 13578147-A-T **
17450284-A-G 15338404-A-G **
18138102-AAAG-A 16026222-AAAG-A FT262970 **
18761952-A-G 16650072-A-G **
19048391-A-T 16936511-A-T **
22486860-C-T 20324974-C-T BY174811 DYZ19 **
23008067-T-C 20846181-T-C FT357940 **
9845309-CAT-C,CAC 10007700-CAT-C,CAC ***
15026658-A-ATT 12914746-A-ATT 13×T***
11643677-CGGAAT-C ***
8663709-CA-C,CAA 8795668-CA-C,CAA 14×A***
14825125-CTTT-C,CTT 12713192-CTTT-C,CTT 20×T***
13457948-T-TATACTGCAC 11302272-T-TATACTGCAC 5×TCCAC***
13457947-A-C 11302271-A-C ***
16687371-AT-A 14575491-AT-A 9×T***
6464185-C-T 6596144-C-T ***
3887957-GT-G 4019916-GT-G 10×T***
2900461-T-C 3032420-T-C ***
3125107-G-T 3257066-G-T ***
4393829-G-GA 4525788-G-GA 8×A***
6029743-T-C 6161702-T-C ***
6418222-C-T 6550181-C-T ***
8274022-AT-A 8405981-AT-A ***
14233378-CT-C 12112672-CT-C ***
14835271-G-A 12723338-G-A ***
15380535-T-A 13268655-T-A ***
15876357-C-A 13764477-C-A ***
16305886-C-G 14194006-C-G ***
21075978-G-A 18914092-G-A FTB40656 ***
21494961-T-C 19333075-T-C ***
21589405-C-T 19427519-C-T ***
24420858-A-G 22274711-A-G ***
9224-C-T ***
9243-G-T ***

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.