Tree Position

R-P312/S116 > Z290 > L21/S145 > S552 > DF13 > ZZ10

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
79183
4308131-A-G 4440090-A-G A+
4452295-T-C 4584254-T-C A+
10629270-C-T A+
19840107-A-G 17728227-A-G P5_Prx A*
18319095-A-G 16207215-A-G P6_Prx A*
20767028-T-G 18605142-T-G P4_Prx A*
6321019-A-C 6452978-A-C IR3_Dst A*
20695092-A-G 18533206-A-G P4_Prx A*
19811171-C-T 17699291-C-T P5_Prx A*
18272240-T-A 16160360-T-A P6_Prx A*
25562933-C-A 23416786-C-A P1_gr1 A*
25585577-G-A 23439430-G-A P1_gr1 A*
26176347-G-A 24030200-G-A P1_Y1 A*
23176803-G-GGAA 21014917-G-GGAA A*
19760604-C-T 17648724-C-T P5_Prx A*
6171910-G-A 6303869-G-A IR3_Dst A*
9732592-T-C 9894983-T-C FT60032 IR3_Prx +
22460497-T-A 20298611-T-A FT457687 DYZ19 +
8884055-G-A 9016014-G-A FT60017 Y+
10647712-C-T FT428113 +
10981428-C-T FT439059 +
8854565-G-A 8986524-G-A BY76366 YY+
10999271-C-T FT439826 +
22476068-C-G 20314182-C-G FT459823 DYZ19 +
8670588-G-A 8802547-G-A FT60012 YY+
19416918-C-A 17305038-C-A FT60280 YY+
13211636-C-T 11055960-C-T PF7439 +
21250254-T-A 19088368-T-A FT60293 YY+
14172249-C-T 12051543-C-T FT60067 YY+
14853321-G-A 12741387-G-A FT60095 YY+
8298558-G-A 8430517-G-A FT60000 YY+
16613161-G-T 14501281-G-T FT60172 YY+
16944112-TTTGG-T 14832232-TTTGG-T +
17706489-A-C 15594609-A-C FT60207 YY+
18021792-G-A 15909912-G-A FT60224 Y+
18392294-C-A 16280414-C-A FT60236 P6_Gap +
18680739-C-A 16568859-C-A BY1456 YY+
18825230-T-C 16713350-T-C FT60253 YY+
18941531-T-C 16829651-T-C FT60256 YY+
19111019-TA-T 16999139-TA-T +
8600716-G-C 8732675-G-C FT60009 YY+
7645258-G-A 7777217-G-A FT59968 YY+
22700267-C-T 20538381-C-T BY192007 YY+
28475650-A-G 26329503-A-G FT60401 +
3435711-T-C 3567670-T-C FT59776 +
24005845-A-G 21859698-A-G FT60395 Y+
3851297-T-C 3983256-T-C FT59803 +
4058784-C-T 4190743-C-T FT59813 +
4458071-C-A 4590030-C-A FT59830 +
4497415-C-G 4629374-C-G FT59831 +
4567441-C-T 4699400-C-T FT59834 +
23652029-T-G 21490143-T-G FT60388 Y+
8094426-C-T 8226385-C-T FT59988 YY+
10799945-GCACTC-G +
5339126-C-G 5471085-C-G FT59870 +
5970231-A-T 6102190-A-T FT59901 +
6027115-T-C 6159074-T-C FT59908 +
28710596-G-A 26564449-G-A FT60409 Y+
6027244-G-C 6159203-G-C FT59909 +
6447580-C-A 6579539-C-A FT59920 +
23509174-C-T 21347288-C-T FT60380 YY+
6703803-T-C 6835762-T-C FT59929 YY+
6791122-G-A 6923081-G-A FT59933 Y+
23438082-T-C 21276196-T-C FT60376 YY+
6914582-A-G 7046541-A-G FT59937 YY+
7021413-C-A 7153372-C-A FT59942 Y+
23239283-G-A 21077397-G-A FT60372 Y+
19430350-G-C 17318470-G-C FT60282 YY+
3385625-A-G 3517584-A-G FT59773 +
26106164-A-G 23960017-A-G P1_Y1 *
5198719-A-G 5330678-A-G *
3571228-G-A 3703187-G-A *
21012190-ATGTGTGTGTGTGTG-A 18850304-ATGTGTGTGTGTGTG-A P4_Dst 20×TG*
24259939-C-A 22113792-C-A P3_b1 **
21216979-A-G 19055093-A-G **
28545624-C-T 26399477-C-T **
21789984-T-A 19628098-T-A **
28799461-GTGAAA-G 26653314-GTGAAA-G **
13459175-G-GCACACGGGTC 11303499-G-GCACACGGGTC **
19522110-T-A 17410230-T-A **
13482172-C-G 11326496-C-G **
7159228-T-C 7291187-T-C **
19000600-A-G 16888720-A-G **
28519485-G-A 26373338-G-A **
13333538-C-T 11177862-C-T **
4763600-T-C 4895559-T-C **
13421388-A-G 11265712-A-G **
14056855-A-G 11936149-A-G **
14267386-A-G 12146680-A-G **
2888803-G-A 3020762-G-A FGC12805 **
15142413-T-C 13030500-T-C **
26834745-GAAGAAAGAAAGAAAGA-G 24688598-GAAGAAAGAAAGAAAGA-G P1_g2 12×AAGA**
18178010-T-A 16066130-T-A **
6495124-T-C 6627083-T-C **
11643742-TG-GT ***
2649802-C-CA 2781761-C-CA 24×A***
10958818-CTCCAT-C ***
23111677-G-A 20949791-G-A ***
18095726-CTA-C 15983846-CTA-C ***
3755208-TA-T 3887167-TA-T 9×A***
7583274-G-GAA 7715233-G-GAA 8×A***
6822204-C-T 6954163-C-T ***
23209249-G-GA 21047363-G-GA 9×A***
23106037-C-A 20944151-C-A ***
8167421-G-A 8299380-G-A ***
13218966-CAAAAAAA-C,CAAAAA 11063290-CAAAAAAA-C,CAAAAA 21×A***
22252012-G-A 20090126-G-A DYZ19 ***
21056039-T-G 18894153-T-G ***
14377959-A-G 12257255-A-G ***
15921580-C-T 13809700-C-T ***
21270206-CAG-C 19108320-CAG-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.

Age Analysis Information (work in progress)

AllMcDonaldYFull
Kit: 791831499984893902408317813
Used in age calculations1499984893902408317813
Counts of SNPs2723
Variant counts last updated 2021-03-28 03:00:14.



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