Tree Position

R-P312/S116 > Z40481 > ZZ11 > U152/S28 > Z56 > BY3548 > Z43/S366 > Z144 > BY3951

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
22291998-A-C 20130112-A-C DYZ19 A+
18366371-T-C 16254491-T-C FGC29057 P6_Prx A*
13687668-A-ATGG 11531992-A-ATGG A*
3988416-A-G 4120375-A-G A*
22315828-A-T 20153942-A-T BY46343 DYZ19 A*
24266321-A-C 22120174-A-C P3_b1 A*
25546120-C-A 23399973-C-A P1_gr1 A*
25887310-A-G 23741163-A-G P1_Y1 A*
25893971-A-G 23747824-A-G P1_Y1 A*
26069029-T-C 23922882-T-C P1_Y1 A*
26080528-A-C 23934381-A-C P1_Y1 A*
26305417-A-T 24159270-A-T P1_Y1 A*
26307965-A-C 24161818-A-C P1_Y1 A*
13660175-C-T 11504499-C-T BY34011FGC1819 GT44026 +
15758479-C-T 13646599-C-T FGC3236FGC3246 YY+
3079326-G-C 3211285-G-C FT165422 +
3317634-T-TA 3449593-T-TA +
3644130-G-A 3776089-G-A FT165692 +
4358401-T-C 4490360-T-C FT166060 +
4450004-A-G 4581963-A-G FT166097 +
4530666-A-G 4662625-A-G FT166138 +
6716058-G-A 6848017-G-A YY+
7077311-C-T 7209270-C-T YY+
7170289-A-C 7302248-A-C FT167276 Y+
7515292-T-C 7647251-T-C FT167404 Y+
7730982-T-C 7862941-T-C FT167492 YY+
7738870-A-G 7870829-A-G FT167498 YY+
8192090-C-G 8324049-C-G FT167652 YY+
8410842-A-T 8542801-A-T FT167751 YY+
8445722-A-G 8577681-A-G FT167767 YY+
10848046-GCATTCCATTC-G +
10848448-A-G +
10957899-A-T FT438167 +
13685080-T-C 11529404-T-C +
14025229-A-G 11904523-A-G FT168369 YY+
14331686-G-A 12210980-G-A FT168542 YY+
15623295-A-G 13511415-A-G FT168977 YY+
15848525-G-GA 13736645-G-GA 8×A+
16175817-A-T 14063937-A-T FT169165 Y+
16457682-T-G 14345802-T-G FT169287 YY+
17009139-A-G 14897259-A-G FT169502 YY+
17309966-G-A 15198086-G-A FT169619 YY+
17632204-G-T 15520324-G-T FT169754 YY+
17638048-A-G 15526168-A-G FT169757 YY+
17872974-G-C 15761094-G-C FT169845 YY+
19066730-C-T 16954850-C-T BY125954 YY+
21298559-G-T 19136673-G-T FT170576 YY+
21508804-A-G 19346918-A-G FT170668 YY+
21856050-T-C 19694164-T-C FT170817 YY+
21954536-G-T 19792650-G-T FT170855 YY+
22464780-T-A 20302894-T-A FT458439 DYZ19 +
22588808-G-T 20426922-G-T FT171010 YY+
23465243-T-A 21303357-T-A FT171325 Y+
26400507-G-A 24254360-G-A P1_Y1 +
28562717-T-A 26416570-T-A FT171611 +
28629962-T-C 26483815-T-C FT171637 +
4163012-G-GCTCCCT 4294971-G-GCTCCCT 7×CTCCCT*
8725757-TCTCACA-T,TCA 8857716-TCTCACA-T,TCA *
4976605-A-G 5108564-A-G **
7411657-T-A 7543616-T-A FT130341 **
4503366-T-C 4635325-T-C **
4503374-C-T 4635333-C-T **
6018632-A-G 6150591-A-G **
6637145-A-G 6769104-A-G FT178665 **
13566448-A-C 11410772-A-C **
14134166-G-A 12013460-G-A **
22506136-A-T 20344250-A-T DYZ19 **
22838670-G-GAAA 20676784-G-GAAA 11×A**
24961177-G-A 22815030-G-A g1 **
26480319-C-T 24334172-C-T P1_Y1 **
3999813-ATG-A 4131772-ATG-A ***
2649802-CAAAAAA-C,CAAAA 2781761-CAAAAAA-C,CAAAA 24×A***
13460583-C-T 11304907-C-T ***
4848351-A-AAT,AATAT 4980310-A-AAT,AATAT 16×AT***
9766591-T-C 9928982-T-C ***
13257268-GAT-G,GATAT 11101592-GAT-G,GATAT 11×AT***
13460567-T-C 11304891-T-C ***
22537275-CA-C,CAAA 20375389-CA-C,CAAA 15×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.