Tree Position

A0-T-YP2191 > P305[A1] > A1b > BT/A1b2 > M168/PF1416[CT] > P143[CF] > M89/PF2746[F] > F1329/M3658[GHI > M201/PF2957[G] > Exact position not yet finalized.

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
NA18549
22476947-G-A 20315061-G-A BY44007 DYZ19 +
22867545-A-T 20705659-A-T Z150Z26720 YY+
2839565-C-T 2971524-C-T YY+
3355705-C-T 3487664-C-T FT316933 +
3589616-G-A 3721575-G-A FT317838 +
4356011-T-A 4487970-T-A FT320377 +
4501198-G-C 4633157-G-C +
5168868-T-A 5300827-T-A FT322972 +
5175842-G-A 5307801-G-A FT322990 +
5250705-A-G 5382664-A-G FT323245 +
5484685-C-A 5616644-C-A FT324058 +
6871886-A-T 7003845-A-T F15401 YY+
7192070-G-A 7324029-G-A CTS1088 YY+
7429388-C-T 7561347-C-T CTS1475 YY+
7558892-G-A 7690851-G-A F15958 YY+
7565836-A-G 7697795-A-G F15964 YY+
7610482-T-G 7742441-T-G F16020 YY+
7700056-G-A 7832015-G-A F16149 YY+
7809328-C-T 7941287-C-T F16273 YY+
7946560-G-A 8078519-G-A F16465 YY+
7970778-G-C 8102737-G-C F16497 YY+
8517923-C-T 8649882-C-T YY+
9774698-T-C 9937089-T-C Y+
10037966-G-A 10200357-G-A BY209673 +
13225770-C-T 11070094-C-T +
13516460-G-C 11360784-G-C +
13552627-G-A 11396951-G-A +
13553505-C-G 11397829-C-G +
13558066-C-T 11402390-C-T +
13560183-A-G 11404507-A-G +
13591837-C-A 11436161-C-A +
13676470-T-C 11520794-T-C +
13814537-G-C 11693831-G-C +
14180957-A-C 12060251-A-C FT300827 Y+
14546884-G-T 12435085-G-T YY+
14985353-C-T 12873421-C-T F19443 YY+
15052976-A-G 12941067-A-G FT301070 YY+
15634018-A-T 13522138-A-T CTS4409 YY+
15741715-T-C 13629835-T-C CTS4634 Y+
15771428-T-C 13659548-T-C F20128 YY+
15930370-T-C 13818490-T-C F20285 YY+
16040015-T-C 13928135-T-C YY+
16086535-A-G 13974655-A-G CTS5251 Y+
16280196-C-G 14168316-C-G F20518 YY+
16582849-C-T 14470969-C-T CTS5968 YY+
16600929-G-A 14489049-G-A CTS5994 YY+
16705758-A-G 14593878-A-G Y+
16802622-G-A 14690742-G-A F21085 YY+
17095626-G-A 14983746-G-A CTS6759 Y+
17266592-G-T 15154712-G-T CTS7064 Y+
17327275-G-A 15215395-G-A CTS7157 YY+
17333962-G-A 15222082-G-A YY+
17484249-A-G 15372369-A-G CTS7443 Y+
17487557-A-G 15375677-A-G F21821 YY+
17728562-C-T 15616682-C-T Y+
17799930-T-A 15688050-T-A F22131 YY+
17971188-C-G 15859308-C-G CTS8388 YY+
18033991-C-T 15922111-C-T F22366 YY+
18035329-G-T 15923449-G-T Y131112 YY+
18987719-T-C 16875839-T-C Y+
19213583-T-G 17101703-T-G CTS10024 Y+
19283955-T-A 17172075-T-A F23536 YY+
19465125-G-C 17353245-G-C F23716 YY+
19501113-C-T 17389233-C-T F23757 YY+
19541788-G-A 17429908-G-A FT302198 Y+
20832674-G-A 18670788-G-A FT302217 P4_Gap +
20959377-C-G 18797491-C-G P4_Dst +
21312882-A-G 19150996-A-G Z1814 YY+
21359175-G-T 19197289-G-T YY+
21418882-A-G 19256996-A-G Y+
21724139-T-A 19562253-T-A F24640 YY+
21855196-A-C 19693310-A-C YY+
22032794-C-T 19870908-C-T YY+
22038617-C-T 19876731-C-T F24959 YY+
22044210-C-T 19882324-C-T F24964 YY+
22119575-C-A 19957689-C-A F25045 YY+
22222469-A-G 20060583-A-G DYZ19 +
22243968-T-C 20082082-T-C DYZ19 +
22510651-C-G 20348765-C-G DYZ19 +
22622994-T-A 20461108-T-A Y+
22654037-C-G 20492151-C-G F25335 YY+
23648358-C-T 21486472-C-T Y+
23794517-G-C 21632631-G-C F26386 Y+
28730486-G-A 26584339-G-A +
28771606-G-A 26625459-G-A CTS12973 +
28789201-G-A 26643054-G-A +

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.