Tree Position

R-P312/S116 > Z40481 > ZZ11 > DF27/S250 > ZZ12 > BY3332 > PH4023 > BY35077

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
56836453-C-T A*
10942687-C-T A*
19660111-G-A 17548231-G-A P5_Prx A*
22257083-C-A 20095197-C-A DYZ19 A*
22290933-G-T 20129047-G-T DYZ19 A*
22319749-C-A 20157863-C-A DYZ19 A*
22319746-T-G 20157860-T-G DYZ19 A*
22257080-T-G 20095194-T-G DYZ19 A*
6192746-C-A 6324705-C-A IR3_Dst A*
25550992-G-C 23404845-G-C P1_gr1 A*
26122932-G-A 23976785-G-A P1_Y1 A*
13447946-T-TATTCC 11292270-T-TATTCC A*
10677045-C-G A*
15914409-C-A 13802529-C-A FT30146 YY+
15802467-T-C 13690587-T-C FT30126 YY+
15678270-T-C 13566390-T-C FT30081 Y+
8892463-A-T 9024422-A-T FT29356 Y+
15560350-A-C 13448470-A-C FT30059 YY+
11648784-A-G FT47020 +
14822749-T-C 12710816-T-C FT29884 YY+
13975486-T-C 11854780-T-C FT29617 Y+
9943032-A-T 10105423-A-T FT47016 Y+
13284468-G-T 11128792-G-T FT47019 +
16837758-C-T 14725878-C-T FT30358 YY+
14175646-G-T 12054940-G-T BY93578 YY+
16378553-A-G 14266673-A-G FT30252 YY+
18833890-AT-A 16722010-AT-A +
16840744-G-A 14728864-G-A BY177651 YY+
23311912-A-G 21150026-A-G FT31621 YY+
28618118-A-G 26471971-A-G FT31861 Y+
24397694-A-G 22251547-A-G FT31791 Y+
23843021-A-AT 21681135-A-AT +
23623951-C-T 21462065-C-T YY+
23589965-C-T 21428079-C-T FT31692 YY+
23500026-T-G 21338140-T-G FT31672 YY+
23147806-A-G 20985920-A-G FT31593 YY+
16865788-C-T 14753908-C-T FT30365 YY+
22609037-T-G 20447151-T-G FT31458 YY+
22256715-G-T 20094829-G-T FT453865 DYZ19 +
21839965-T-A 19678079-T-A Y+
8573092-T-C 8705051-T-C FT29265 YY+
18251991-C-T 16140111-C-T BY20623 Y+
17599239-C-T 15487359-C-T FT30589 YY+
17333215-C-A 15221335-C-A FT30485 YY+
8673423-C-T 8805382-C-T FT29296 Y+
11007361-T-C FT47018 +
8449479-T-C 8581438-T-C FT29232 YY+
5397363-G-C 5529322-G-C FT28390 +
13805282-T-G 11684576-T-G FT47017 +
19537190-C-T 17425310-C-T FT31074 YY+
2762285-T-A 2894244-T-A YY+
3110400-C-G 3242359-C-G FT27498 +
3220388-A-G 3352347-A-G FT27536 +
3528006-A-G 3659965-A-G FT27651 +
8421164-C-CTT 8553123-C-CTT +
4147462-C-T 4279421-C-T FT27904 +
4275621-C-T 4407580-C-T FT27949 +
4361518-A-C 4493477-A-C FT27989 +
4696513-C-A 4828472-C-A FT28109 +
4699120-A-T 4831079-A-T FT28111 +
3693823-C-T 3825782-C-T FT27729 +
6400757-T-C 6532716-T-C FT28708 +
7417939-G-C 7549898-G-C FT28959 YY+
8062051-G-C 8194010-G-C FT29120 Y+
7698694-TTA-T 7830653-TTA-T +
7419960-G-C 7551919-G-C FT28960 YY+
7855738-AG-A 7987697-AG-A +
7236060-G-A 7368019-G-A FT28923 YY+
6471657-GAA-G 6603616-GAA-G +
28813812-AGGAAT-A 26667665-AGGAAT-A 5×GGAAT*
8075953-T-C 8207912-T-C Y*
10692519-CTCCAT-C *
22432857-G-A 20270971-G-A DYZ19 *
22340458-G-A 20178572-G-A DYZ19 *
22317175-G-C 20155289-G-C DYZ19 *
22312568-A-G 20150682-A-G BY217104 DYZ19 *
3997018-T-TAAC 4128977-T-TAAC 9×AAC*
4488795-G-T 4620754-G-T *
5356092-C-CA 5488051-C-CA 8×A**
9832630-A-G 9995021-A-G Y21657 **
27546113-C-T 25399966-C-T P1_Y2 **
25520291-C-A 23374144-C-A P1_gr1 **
10474005-G-A **
17997742-G-C 15885862-G-C P7_Gap **
13476344-A-T 11320668-A-T **
20677847-C-A 18515961-C-A P4_Prx **
15101361-T-C 12989449-T-C **
9804663-G-A 9967054-G-A ***
10973868-CAGTT-C ***
16214725-G-A 14102845-G-A ***
17787106-CAAAAA-C 15675226-CAAAAA-C 19×A***
4826445-C-T 4958404-C-T FT321827 ***
19138376-AAT-A 17026496-AAT-A ***
24689891-C-T 22543744-C-T P3_b2 ***
13476331-G-T 11320655-G-T ***
10654083-TTCCACTCCAC-T ***
13446606-A-AC 11290930-A-AC ***
56871650-ATGAGA-T ***
23034293-CTT-C,CT 20872407-CTT-C,CT 15×T***
15012296-CTTT-C,CTT 12900384-CTTT-C,CTT 17×T***
13457387-C-T 11301711-C-T ***
6150009-GTATATATA-G,GTA 6281968-GTATATATA-G,GTA IR3_Dst 19×TA***
9949969-T-C 10112360-T-C ***
13340398-G-C 11184722-G-C ***
13600975-A-G 11445299-A-G ***
56756815-A-T ***

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.

Age Analysis Information (work in progress)

Kit: 1297631523954595374438379872
Used in age calculations1523954595374438379872
Counts of SNPs3128
Variant counts last updated 2022-07-13 02:36:59.

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