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
NA18558
3547516-G-C 3679475-G-C +
14399100-C-CCA 12278394-A-AC +
3311122-G-T 3443081-G-T FT316792 +
3341190-G-A 3473149-G-A +
3345808-T-C 3477767-T-C FT316892 +
3473158-G-C 3605117-G-C FT317376 +
3544721-C-T 3676680-C-T FT317648 +
3592837-A-G 3724796-A-G FT317846 +
3981116-T-C 4113075-T-C FT319123 +
4175900-T-C 4307859-T-C FT319773 +
4322153-T-C 4454112-T-C FT320288 +
4332425-A-C 4464384-A-C FT320318 +
4641318-T-A 4773277-T-A +
4697960-G-A 4829919-G-A FT321446 +
4755136-T-C 4887095-T-C FT321652 +
5081728-G-A 5213687-G-A FT322655 +
5097075-G-C 5229034-G-C FT322718 +
5222003-C-A 5353962-C-A FT323141 +
5494114-C-A 5626073-C-A FT324087 +
5654065-C-T 5786024-C-T FT324649 +
6009810-C-T 6141769-C-T FT325846 +
6083200-T-A 6215159-T-A FT326087 +
6400947-G-A 6532906-G-A FGC34037 +
6456816-C-G 6588775-C-G FT326610 +
6733280-G-A 6865239-G-A YY+
6844772-C-T 6976731-C-T PH231 YY+
6932254-G-C 7064213-G-C SK2267 FGC15577 YY+
7098499-A-T 7230458-A-T FT300064 Y+
7100158-G-T 7232117-G-T FT300065 Y+
7272126-A-G 7404085-A-G PH571 YY+
7303545-G-C 7435504-G-C FT300112 Y+
7305271-GCA-G 7437230-GCA-G +
7377874-A-T 7509833-A-T CTS1392 YY+
7552272-A-G 7684231-A-G F15946 YY+
7610608-A-T 7742567-A-T V1267 YY+
7651424-C-T 7783383-C-T YY+
7674144-T-C 7806103-T-C V1359 YY+
7902473-T-C 8034432-T-C F16400 YY+
7968280-T-G 8100239-T-G FT300293 Y+
8111518-C-A 8243477-C-A FT300338 Y+
8208621-G-T 8340580-G-T YY+
8348525-A-C 8480484-A-C F16927 YY+
8732768-C-T 8864727-C-T FT80736 Y+
8769916-G-A 8901875-G-A F17467 YY+
8777729-C-A 8909688-C-A F17478 YY+
9047817-C-T 9210208-C-T +
9978716-A-C 10141107-A-C Y+
13304581-T-C 11148905-T-C +
13312266-C-T 11156590-C-T +
13359823-T-A 11204147-T-A +
13388142-A-C 11232466-A-C +
13438534-C-A 11282858-C-A +
13531255-T-C 11375579-T-C +
13550956-T-A 11395280-T-A +
13661475-G-A 11505799-G-A FGC32480 +
13712668-G-A 11556992-G-A +
13834859-G-A 11714153-G-A FT328615 +
13852973-G-T 11732267-G-T FT328754 +
13905452-C-T 11784746-C-T PH696 Y+
13945322-C-T 11824616-C-T PH732 YY+
14006721-G-A 11886015-G-A FGC65416 F18328 YY+
14240330-C-A 12119624-C-A FT300852 YY+
14405806-C-T 12285103-C-T F18919 YY+
14745159-A-G 12633228-A-G PH1439 V2567 YY+
14886768-T-C 12774834-T-C PH1493 V2660 YY+
15120828-G-A 13008915-G-A Y+
15462190-A-C 13350310-A-C YY+
15503340-C-A 13391460-C-A F19857 YY+
15783915-T-C 13672035-T-C F20153 YY+
15901214-C-G 13789334-C-G PH1887 YY+
15975816-T-A 13863936-T-A PH1935 YY+
16065714-C-T 13953834-C-T FT301321 Y+
16382642-A-G 14270762-A-G FT301383 Y+
16523776-T-A 14411896-T-A PH2333 YY+
16739664-G-C 14627784-G-C FT301470 YY+
16849695-C-T 14737815-C-T PH2606 YY+
16934195-G-C 14822315-G-C PH2681 YY+
17207699-A-G 15095819-A-G PH2893 YY+
17258905-C-G 15147025-C-G Y+
17377567-C-T 15265687-C-T FT301618 Y+
17581508-G-A 15469628-G-A PH3202 YY+
17759694-T-A 15647814-T-A PH3353 YY+
17886508-A-G 15774628-A-G F22241 YY+
17919221-G-A 15807341-G-A PH3512 YY+
17939611-C-T 15827731-C-T CTS8332 YY+
18037727-A-G 15925847-A-G YY+
18087665-A-T 15975785-A-T F22430 YY+
18088249-A-G 15976369-A-G YY+
18112476-T-G 16000596-T-G PH3704 YY+
18154938-G-C 16043058-G-C F22510 YY+
18623163-G-C 16511283-G-C FT301925 Y+
18687655-A-G 16575775-A-G FT301942 YY+
18706069-A-G 16594189-A-G V3423 YY+
18780711-T-A 16668831-T-A FT301968 YY+
18875317-C-T 16763437-C-T FT301995 Y+
18931521-T-C 16819641-T-C PH4100 V3617 YY+
18992204-G-A 16880324-G-A PH4134 V3666 YY+
19036070-G-A 16924190-G-A PH4165 YY+
19241444-T-A 17129564-T-A CTS10070 YY+
19254396-G-A 17142516-G-A F23501 YY+
19306933-T-G 17195053-T-G F23554 YY+
21157482-A-T 18995596-A-T SK2264 Y+
21262409-C-T 19100523-C-T F24066 YY+
21302872-G-A 19140986-G-A F24119 YY+
21303506-A-C 19141620-A-C F24120 YY+
21332749-C-T 19170863-C-T FT302308 YY+
21405840-A-T 19243954-A-T BZ659 YY+
21459185-A-G 19297299-A-G Y+
21494506-G-T 19332620-G-T F24373 YY+
21610962-G-C 19449076-G-C YY+
21647270-G-A 19485384-G-A F24543 YY+
21852885-C-A 19690999-C-A F24754 YY+
21867887-C-A 19706001-C-A PH4986 YY+
21887087-A-G 19725201-A-G FT302513 Y+
22080067-C-T 19918181-C-T F25000 YY+
22092123-C-T 19930237-C-T F25020 YY+
22131003-G-A 19969117-G-A FT302587 YY+
22444338-C-T 20282452-C-T DYZ19 +
22476537-G-A 20314651-G-A FT459873 DYZ19 +
22476854-G-T 20314968-G-T ZS2549 DYZ19 +
22887604-C-T 20725718-C-T PH5230 YY+
23487663-A-G 21325777-A-G PH5435 YY+
23828843-A-G 21666957-A-G FT302992 Y+
23980709-C-T 21834562-C-T F26548 Y+
24395041-T-G 22248894-T-G Y+
28549501-G-A 26403354-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.