Tree Position

R-P312/S116 > Z290 > L21/S145 > S552 > DF63/S522 > BY592 > CTS5454 > Z16245 > Z16246 > BY3070 > FT72783 > FGC36423 > FGC36422 > BY7776 > BY7771

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 STR1kG
5702646-G-A 5834605-G-A +
13222796-G-C 11067120-G-C +
15066209-GA-G 12954300-GA-G +
14910819-TG-T 12798886-TG-T +
14625227-TAAATAC-T 12513427-TAAATAC-T +
14261562-C-G 12140856-C-G YY+
13534808-G-A 11379132-G-A FT444925 +
13384939-T-C 11229263-T-C +
13346071-C-CAA 11190395-C-CAA 18×A+
13222768-A-T 11067092-A-T +
15557161-ATT-A 13445281-ATT-A +
13222699-A-C 11067023-A-C +
9789274-ACG-A 9951665-ACG-A +
9524011-GTA-G 9686402-GTA-G +
6698845-G-T 6830804-G-T YY+
6359151-G-A 6491110-G-A +
5797428-A-T 5929387-A-T +
5400468-C-CTT 5532427-C-CTT 19×T+
15557160-TATTC-T 13445280-TATTC-T +
15733904-AG-A 13622024-AG-A +
5038227-G-A 5170186-G-A FT162428 +
22802868-A-ATTTTTTT 20640982-A-ATTTTTTT 32×T+
27484258-ATCTTTCTT-A 25338111-ATCTTTCTT-A P1_Y2 19×TCTT+
26478049-G-A 24331902-G-A FT183068 P1_Y1 +
25173627-C-T 23027480-C-T g1 +
25173622-G-A 23027475-G-A BY184332 g1 +
24447211-C-G 22301064-C-G Y+
23819106-G-T 21657220-G-T M1973 Y+
23317649-C-CTTTTTT 21155763-C-CTTTTTT 37×T+
22533900-G-A 20372014-G-A Y+
16364105-TATATATAC-T 14252225-TATATATAC-T +
22287203-T-C 20125317-T-C DYZ19 +
22241745-A-G 20079859-A-G DYZ19 +
19231310-TC-T 17119430-TC-T +
19189430-C-CTTTT 17077550-C-CTTTT 35×T+
18001245-A-G 15889365-A-G FTA9335 P7_Gap Y+
17081244-TATAA-T 14969364-TATAA-T +
16651878-G-C 14539998-G-C YY+
5252849-TG-T 5384808-TG-T +
4976705-A-G 5108664-A-G MF2798 +
3838601-C-CTTT 3970560-C-CTTT 31×T+
7633048-G-T 7765007-G-T FT345375 YY+
15793046-A-G 13681166-A-G FT346755 Y+
15524063-C-T 13412183-C-T FT346661 YY+
15048170-A-T 12936261-A-T FT346527 YY+
14520522-G-A 12408723-G-A BY201634 YY+
14039063-A-G 11918357-A-G FT346145 YY+
14033930-G-A 11913224-G-A FT160078 YY+
8080049-T-A 8212008-T-A FT162853 YY+
14881734-A-G 12769802-A-G YY+
16000895-T-G 13889015-T-G FT346818 Y+
14396417-C-A 12275713-C-A FT175198 YY13×A+
19146564-C-T 17034684-C-T YY+
21894650-T-A 19732764-T-A YY+
21853677-C-CAAAAAA 19691791-C-CAAAAAA 43×A+
15966320-G-A 13854440-G-A F20329 YY+
16974655-A-T 14862775-A-T Y+
4642516-A-G 4774475-A-G FTA9334 +
3523642-A-G 3655601-A-G +
4303928-A-G 4435887-A-G +
4232799-T-C 4364758-T-C FT162276 +
4177136-TTA-T 4309095-TTA-T +
4145499-T-C 4277458-T-C +
4067395-AG-A 4199354-AG-A +
3900571-G-C 4032530-G-C FT162200 +
3892102-A-G 4024061-A-G FT77988 +
3500420-C-T 3632379-C-T +
17053491-C-T 14941611-C-T FT347221 YY+
3279492-T-C 3411451-T-C YFS028084 F8648 +
3072529-A-G 3204488-A-G FT162034 +
21920197-T-A 19758311-T-A FT348516 Y+
21357662-T-A 19195776-T-A FT348317 YY+
21132485-C-T 18970599-C-T FT348225 YY+
21055246-A-T 18893360-A-T FT348202 Y+
18964126-C-T 16852246-C-T FT293981 YY+
17513761-A-G 15401881-A-G FTA6060 YY+
28554575-A-C 26408428-A-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.

Mutation Notes:

Manual22907114-TC-T20745228-TC-T9 reads in total. 8 show the deletion, and one read is clearly in the wrong spot.
Manual15964932-A-AT13853052-A-ATThis is a short 5T sequence. 2 reads cover the whole sequence and both show the insertion.
Manual19900207-A-G17788327-A-G3A 3G

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