Tree Position

R-U106/S21 > Z2265 > Z381/S263 > Z301/S499 > L48 > L47/S170 > Z160 > S3251 > 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 STRFTDNA
N41915
BigY3
N41915
9658064-T-TA 9820455-T-TA IR3_Prx 8×AA+
19984860-C-T 17872980-C-T P5_Prx ***A*
18375500-G-GA 16263620-G-GA P6_Prx ***A*
20612935-C-T 18451049-C-T P4_Prx ***A*
22257018-G-T 20095132-G-T DYZ19 ***A*
25912789-A-G 23766642-A-G P1_Y1 ***A*
25935847-T-G 23789700-T-G P1_Y1 ***A*
26043054-G-A 23896907-G-A P1_Y1 ***A*
18480043-G-GAA 16368163-G-GAA P6_Dst 17×AA*
3181374-T-C 3313333-T-C A*
20414083-T-A 18252197-T-A P5_Dst A*
20414086-G-C 18252200-G-C P5_Dst A*
20414089-T-A 18252203-T-A P5_Dst A*
3066613-G-A 3198572-G-A A*
18433576-C-CT 16321696-C-CT P6_Dst A*
22319684-G-T 20157798-G-T DYZ19 A*
25561308-G-C 23415161-G-C P1_gr1 A*
26368668-C-A 24222521-C-A P1_Y1 A*
56830890-A-C A*
56831253-C-T A*
3436225-T-C 3568184-T-C FGC37003FT274 **+
13861775-C-T 11741069-C-T BY91560 ++
23976843-ATTGT-A 21830696-ATTGT-A +
22444205-G-C 20282319-G-C BY31629 DYZ19 ***+
8193183-C-A 8325142-C-A BY70594 YY++
9095568-C-T 9257959-C-T Y140063 Y++
9102754-C-T 9265145-C-T BY78105 Y++
14234430-C-T 12113724-C-T BY94148 YY++
14853760-A-G 12741826-A-G BY98028 YY++
14909744-A-T 12797811-A-T BY98416 YY++
15329598-G-A 13217716-G-A FT180311 YY++
15604101-T-C 13492221-T-C BY102815 YY++
16250845-G-A 14138965-G-A BY106353 YY++
17547409-C-A 15435529-C-A BY115616 YY++
19154232-G-A 17042352-G-A BY126770 YY++
19388703-T-G 17276823-T-G BY128667 Y++
21780831-C-T 19618945-C-T BY135418 YY++
21864816-G-A 19702930-G-A BY136007 YY++
22009180-G-T 19847294-G-T BY137060 YY++
22020718-T-C 19858832-T-C BY137118 YY++
22462474-T-G 20300588-T-G BY220908 DYZ19 ++
22744804-T-C 20582918-T-C BY140483 YY++
22786486-T-C 20624600-T-C BY140761 YY++
23985611-T-C 21839464-T-C BY149027 Y++
10868880-T-C FT434811 +
4134706-G-A 4266665-G-A FT113399 +
6816797-A-G 6948756-A-G YY+
7137993-GTGTC-G 7269952-GTGTC-G +
8385353-G-A 8517312-G-A FT115815 Y+
9966023-AGAG-A 10128414-AGAG-A +
9975677-T-C 10138068-T-C FT373596 Y+
9981518-C-T 10143909-C-T BY82401 Y+
10021078-CTCTCACTCTTTCTGTT-C 10183469-CTCTCACTCTTTCTGTT-C +
10825765-T-C FT432904 +
10920708-A-T FT436593 +
11643654-G-A FT449702 +
14012591-C-T 11891885-C-T FT116421 Y+
19844857-C-T 17732977-C-T FT452432 P5_Prx +
21522048-A-T 19360162-A-T FT119058 YY+
59009242-C-CA 56863095-C-CA 9×A*
5384665-T-TTTTG 5516624-T-TTTTG 7×TTTG*
22301986-G-C 20140100-G-C DYZ19 ****
27570834-C-T 25424687-C-T P1_Y2 *
4416824-C-T 4548783-C-T *
4346565-ATTTTTTTT-A,AT 4478524-ATTTTTTTT-A,AT 22×T*
6586158-G-GA 6718117-G-GA *
17440464-A-C 15328584-A-C PF850 **
13455576-T-C 11299900-T-C BY85438 **
10628067-T-A **
3561314-C-T 3693273-C-T **
3640682-CTCCTTCCTTCCTTCCTTCCTTCCTTCCTTCCTTCCTTCCT-C 3772641-CTCCTTCCTTCCTTCCTTCCTTCCTTCCTTCCTTCCTTCCT-C 14×TCCT**
4729086-T-C 4861045-T-C **
7345714-C-T 7477673-C-T **
12377194-T-C **
22692240-C-T 20530354-C-T **
22962174-C-T 20800288-C-T **
28812640-C-G 26666493-C-G **
13814132-A-G 11693426-A-G ***
13833837-T-C 11713131-T-C ***
24324722-A-G 22178575-A-G A9063BY25245 P3_t1 ***
25297328-A-G 23151181-A-G P2_r1 ***
6222309-A-AT 6354268-A-AT L627 IR3_Dst 8×T***
13838969-T-A 11718263-T-A FT276859 ***
13863679-C-T 11742973-C-T ***
13659390-T-G 11503714-T-G ***
13659385-T-A 11503709-T-A ***
13863697-T-A 11742991-T-A ***
13833845-A-C 11713139-A-C 5×GGAAT***
7137993-GTGTC-G,GTGTG 7269952-GTGTC-G,GTGTG ***
10021078-CTCTCACTCTTTCTGTT-C,CTCTCTCTCTTTCTATT 10183469-CTCTCACTCTTTCTGTT-C,CTCTCTCTCTTTCTATT ***
22290444-C-T 20128558-C-T DYZ19 ***
22314195-T-C 20152309-T-C DYZ19 ***
22511522-A-C 20349636-A-C DYZ19 ***
23976844-TTGTT-T,TTGTG 21830697-TTGTT-T,TTGTG ***
24814967-C-CTGGCTGT 22668820-C-CTGGCTGT P3_b2 ***
24958123-C-T 22811976-C-T g1 ***
24978110-C-A 22831963-C-A g1 ***
25205466-C-T 23059319-C-T g1 ***
25787440-C-A 23641293-C-A P1_b3 ***
26195231-C-A 24049084-C-A P1_Y1 ***
26962905-G-A 24816758-G-A P1_r3 ***
8389638-A-G 8521597-A-G ***
19202952-AAG-A 17091072-AAG-A ***
13485644-T-A 11329968-T-A ***
10973613-ATTCCG-A ***
23825772-A-T 21663886-A-T ***
7197570-AT-A,ATT 7329529-AT-A,ATT 19×T***
15865946-CTTTTTTTTTTTT-C 13754066-CTTTTTTTTTTTT-C 37×T***
3635962-CA-C 3767921-CA-C ***
4973668-CA-C,CAA 5105627-CA-C,CAA 19×A***
8161256-T-A 8293215-T-A ***
10988455-T-G ***
13444794-A-G 11289118-A-G ***
15497972-ATTTTTT-A,ATTTT 13386092-ATTTTTT-A,ATTTT 26×T***
19203897-A-T 17092017-A-T ***
23241947-CTTTT-C,CT 21080061-CTTTT-C,CT 27×T***
28544249-A-G 26398102-A-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.