Tree Position

A0-T-YP2191 > P305[A1] > A1b > BT/A1b2 > M168/PF1416[CT] > P143[CF] > M89/PF2746[F] > F1329/M3658[GHI > F929[HIJK] > IJK > K > M526[K2] > M2335 > F346[NO] > M2148[N] > 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
NA18748
13867745-C-T 11747039-C-T BY54559 +
21220929-C-T 19059043-C-T Z17585FGC8608 Y19901 Y+
24417101-A-AG 22270954-A-AG +
7617848-G-T 7749807-G-T Y24389 YY+
2983594-C-A 3115553-C-A FT315634 +
3278959-C-G 3410918-C-G FT316683 +
3311693-C-T 3443652-C-T +
3464359-C-T 3596318-C-T FT38421 +
3615632-G-A 3747591-G-A FT38528 +
3844368-C-A 3976327-C-A FT318688 +
4023509-T-C 4155468-T-C FT38788 +
4228450-C-A 4360409-C-A FT319951 +
4233337-A-T 4365296-A-T FT319964 +
4304920-T-A 4436879-T-A FT320215 +
4626943-T-C 4758902-T-C FT321241 +
5214352-C-G 5346311-C-G Y24855 +
5684299-G-T 5816258-G-T FT324759 +
6357661-T-A 6489620-T-A FT326308 +
6401907-C-T 6533866-C-T Y15296 +
6494683-C-T 6626642-C-T FT40112 +
6529160-T-C 6661119-T-C FT40128 +
6640608-T-G 6772567-T-G Y+
6684960-C-A 6816919-C-A FT299965 Y+
6905105-T-C 7037064-T-C Y23789 YY+
7112274-T-G 7244233-T-G CTS962 YY+
7147350-C-T 7279309-C-T CTS1016 YY+
7377669-A-G 7509628-A-G CTS1390 YY+
7684725-G-A 7816684-G-A Y23791 YY+
7836027-G-A 7967986-G-A YY+
8061028-A-G 8192987-A-G FT300324 YY+
8620199-A-G 8752158-A-G F17317 br2 YY+
9398288-G-C 9560679-G-C Y24390 YY+
9645953-C-T 9808344-C-T Y24391 IR3_Prx +
13208400-G-A 11052724-G-A MF1063 +
13371291-C-T 11215615-C-T +
13525090-A-G 11369414-A-G +
13657638-G-C 11501962-G-C +
13669674-T-A 11513998-T-A MF1064 +
13981944-G-T 11861238-G-T Y+
14050955-A-G 11930249-A-G F18399 YY+
14086021-G-T 11965315-G-T Y24392 YY+
14120475-A-G 11999769-A-G CTS1915 Y+
14203192-C-T 12082486-C-T YY+
14253742-C-T 12133036-C-T Y24393 YY+
14287635-G-T 12166929-G-T CTS2389 YY+
14288236-C-T 12167530-C-T CTS2393 YY+
14328239-C-T 12207533-C-T CTS2495 YY+
14488540-G-A 12367809-G-A YY+
14501703-T-C 12389908-T-C FT300953 Y+
14755948-C-G 12644017-C-G MF1065 Y+
14759708-T-C 12647777-T-C Y+
15000499-C-T 12888584-C-T YY+
15207544-G-C 13095630-G-C F19639 YY+
15456288-G-T 13344408-G-T F19801 YY+
15563329-G-A 13451449-G-A CTS4309 YY+
15577617-G-C 13465737-G-C CTS4323 YY+
15656131-G-T 13544251-G-T F20007 YY+
15801823-C-G 13689943-C-G CTS4759 YY+
15877890-G-A 13766010-G-A CTS4864 YY+
16284623-G-A 14172743-G-A CTS5452 YY+
16471680-T-C 14359800-T-C CTS5766 YY+
16779494-G-A 14667614-G-A CTS6261 YY+
17000400-G-A 14888520-G-A CTS6600 Y+
17047610-A-G 14935730-A-G F21333 YY+
17203809-G-T 15091929-G-T YY+
17379520-C-T 15267640-C-T Y+
17413497-C-G 15301617-C-G CTS7304 YY+
17478417-C-G 15366537-C-G Y23793 YY+
18398551-G-C 16286671-G-C Y23794 P6_Gap +
18580800-C-G 16468920-C-G Y23795 YY+
18655851-G-A 16543971-G-A CTS9076 YY+
19053727-T-A 16941847-T-A Y23797 YY+
19123193-T-A 17011313-T-A F23333 YY+
19341948-T-C 17230068-T-C CTS10244 YY+
19490412-G-A 17378532-G-A Y23798 Y+
19556132-C-T 17444252-C-T CTS10583 Y+
21051866-T-C 18889980-T-C YY+
21446828-A-T 19284942-A-T F24310 YY+
21464798-C-G 19302912-C-G YY+
21536263-G-T 19374377-G-T Y+
21646081-C-T 19484195-C-T F24541 YY+
21646566-G-C 19484680-G-C F24542 YY+
21646578-T-C 19484692-T-C YY+
22135431-T-G 19973545-T-G Y24397 YY+
22271838-G-C 20109952-G-C FT315302 DYZ19 +
22457439-T-A 20295553-T-A DYZ19 +
22469611-C-A 20307725-C-A DYZ19 +
22472597-T-A 20310711-T-A FT459348 DYZ19 +
22473916-C-T 20312030-C-T BY223024 DYZ19 +
22478783-G-T 20316897-G-T DYZ19 +
22523578-C-A 20361692-C-A Y+
22530186-C-T 20368300-C-T FT43956 Y+
22664052-G-A 20502166-G-A CTS10622 YY+
22703508-A-G 20541622-A-G YY+
22711069-C-T 20549183-C-T Y23801 YY+
22779442-A-G 20617556-A-G CTS10792 Y+
22986243-C-T 20824357-C-T CTS11169 Y+
23093529-G-A 20931643-G-A FT44158 Y+
23105467-C-T 20943581-C-T FT299215 Y+
23130366-T-A 20968480-T-A Y23802 YY+
23360153-A-T 21198267-A-T FT302875 YY+
23427967-T-C 21266081-T-C F26057 YY+
28766264-C-T 26620117-C-T Y23803 Y+
28787355-A-G 26641208-A-G +
28795899-C-G 26649752-C-G +

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.