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] > P295[P] > M207[R] > M173[R1] > L146/M420[R1a] > M459 > M198 > M417 > Z645 > Z93 > Z94 > Y3 > 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 STRBigY3
MI28199
9708384-C-T 9870775-C-T IR3_Prx A+
22217036-G-C 20055150-G-C DYZ19 A+
28784427-A-T 26638280-A-T A*
58977496-G-A 56831349-G-A A*
6172004-G-A 6303963-G-A IR3_Dst A*
13462397-C-G 11306721-C-G A*
11653786-C-CGAATGGAATG A*
19682411-A-AG 17570531-A-AG P5_Prx A*
19881590-G-T 17769710-G-T P5_Prx A*
19912723-G-C 17800843-G-C P5_Prx A*
20267053-C-G 18105167-C-G P5_Dst A*
22291595-G-T 20129709-G-T DYZ19 A*
25565208-G-A 23419061-G-A P1_gr1 A*
25602298-T-C 23456151-T-C P1_gr1 A*
25980929-C-T 23834782-C-T P1_Y1 A*
26304552-T-C 24158405-T-C P1_Y1 A*
56831949-A-T A*
22474007-G-T 20312121-G-T BY29073 DYZ19 +
16240818-C-T 14128938-C-T FT13284 YY+
2974912-A-G 3106871-A-G FT11480 +
2994308-T-C 3126267-T-C FT11488 +
3362541-C-A 3494500-C-A FT11584 +
3677547-G-A 3809506-G-A FT11666 +
3769514-T-C 3901473-T-C FT11693 +
4272936-A-T 4404895-A-T FT11855 +
4381652-G-A 4513611-G-A FT11881 +
4563936-A-G 4695895-A-G FT11924 +
5125184-T-G 5257143-T-G FT12097 +
5300831-G-A 5432790-G-A FT12152 +
5520627-A-G 5652586-A-G FT12217 +
5609912-C-T 5741871-C-T FT12245 +
5658823-C-T 5790782-C-T FT12268 +
5954215-G-C 6086174-G-C FT12338 +
6446590-G-A 6578549-G-A FT12437 +
6715865-G-A 6847824-G-A FT12493 YY+
6797817-A-G 6929776-A-G FT12504 YY+
7069523-T-A 7201482-T-A FT12531 YY+
7284420-T-C 7416379-T-C FT12565 YY+
7358304-C-T 7490263-C-T YY+
7654382-T-G 7786341-T-G FT12612 YY+
8200727-T-A 8332686-T-A FT12687 YY+
8404950-C-G 8536909-C-G FT12712 YY+
8443809-C-T 8575768-C-T FT12720 YY+
8778844-G-T 8910803-G-T FT12765 YY+
9829937-C-T 9992328-C-T FT12845 YY+
10828296-C-T FT433021 +
14420329-C-T 12299604-C-T FT13027 YY+
14784583-A-C 12672653-A-C FT13087 YY+
14804408-G-A 12692479-G-A FGC2336 YY+
15719751-C-G 13607871-C-G FT13217 YY+
16858175-A-G 14746295-A-G FT13362 YY+
17170419-G-T 15058539-G-T FT13410 YY+
17393275-T-C 15281395-T-C YY+
17518607-T-A 15406727-T-A FT13460 YY+
17813485-T-A 15701605-T-A FT13507 YY+
18649912-G-T 16538032-G-T FT13599 YY+
18840696-T-C 16728816-T-C FT13626 YY+
19201860-T-C 17089980-T-C FT13682 YY+
19204082-TATA-T 17092202-TATA-T +
19546026-A-G 17434146-A-G YY+
21184808-C-T 19022922-C-T FT13765 YY+
21457889-A-C 19296003-A-C FT13824 Y+
21471749-G-T 19309863-G-T FT13829 YY+
21899446-T-C 19737560-T-C FT13914 YY+
22036104-G-A 19874218-G-A FT13945 YY+
22191918-A-T 20030032-A-T FT13965 YY+
22228633-G-T 20066747-G-T FT453134 DYZ19 +
22474819-C-A 20312933-C-A FT459673 DYZ19 +
22512423-A-T 20350537-A-T DYZ19 +
23452141-T-A 21290255-T-A FT14108 YY+
24386681-T-C 22240534-T-C FT14166 +
24432585-C-CCAT 22286438-C-CCAT +
28622563-A-C 26476416-A-C FT14234 Y+
22299407-C-A 20137521-C-A DYZ19 *
10971897-TATTCC-T *
13292445-T-A 11136769-T-A *
22277226-A-T 20115340-A-T BY215726 DYZ19 *
22281023-G-T 20119137-G-T DYZ19 *
27482053-C-G 25335906-C-G P1_Y2 *
27958650-A-G 25812503-A-G P1_Y2 *
20326037-GC-G 18164151-GC-G P5_Dst **
21002536-TC-T 18840650-TC-T P4_Dst **
28819268-G-GTTCCATGGAGT 26673121-G-GTTCCATGGAGT **
28808577-C-G 26662430-C-G **
25601436-G-T 23455289-G-T P1_gr1 8×A**
3873011-A-G 4004970-A-G **
4375410-T-C 4507369-T-C **
6723311-C-T 6855270-C-T **
7457038-T-TA 7588997-T-TA IR1_L **
8110765-C-G 8242724-C-G **
8293292-T-C 8425251-T-C **
13356818-C-T 11201142-C-T **
15857685-T-G 13745805-T-G **
19203927-AATT-A 17092047-AATT-A **
22423710-T-C 20261824-T-C DYZ19 **
22530214-T-A 20368328-T-A **
26349819-C-A 24203672-C-A P1_Y1 **
27937851-A-G 25791704-A-G P1_Y2 **
17794249-T-G 15682369-T-G ***
3790878-GTATATATATA-G 3922837-GTATATATATA-G 21×TA***
4174962-CTTT-C 4306921-CTTT-C 31×T***
17332750-CAAA-C 15220870-CAAA-C 22×A***
13465952-A-C 11310276-A-C ***
15117593-A-G 13005680-A-G ***
13932140-CATATAT-C 11811434-CATATAT-C 13×AT***
4251033-CTT-C,CT 4382992-CTT-C,CT 24×T***
4275279-AC-A 4407238-AC-A ***
5224763-CA-C,CAA 5356722-CA-C,CAA 13×A***
7199342-CTT-C,CT 7331301-CTT-C,CT 24×T***
10673070-T-C ***
10958813-G-GTCCAC ***
14558189-C-CT 12446390-C-CT ***
22517410-C-CA,CAA 20355524-C-CA,CAA 13×A***
24387388-TATATATATATCCC-T,TATATATATATCCCAT 22241241-TATATATATATCCC-T,TATATATATATCCCAT ***
25246421-T-A,C 23100274-T-A,C P2_r1 ***

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.