Tree Position

R-P312/S116 > Z290 > L21/S145 > S552 > DF13 > Z39589 > Y14240 > BY23479 > Y46693

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
5662780-T-C 5794739-T-C A+
28817683-G-C 26671536-G-C A*
28817713-C-T 26671566-C-T A*
26107411-C-A 23961264-C-A P1_Y1 A*
13451560-A-G 11295884-A-G A*
6315724-C-T 6447683-C-T IR3_Dst A*
19685716-C-T 17573836-C-T P5_Prx A*
19879893-A-T 17768013-A-T P5_Prx A*
20737968-A-G 18576082-A-G P4_Prx A*
20749532-G-A 18587646-G-A P4_Prx A*
25887859-G-A 23741712-G-A P1_Y1 A*
28817367-A-T 26671220-A-T A*
17668517-G-T 15556637-G-T PH3265 YY+
23231787-C-T 21069901-C-T BY143840 Y+
16929013-C-T 14817133-C-T Y52549 FGC74753 YY+
21739200-A-G 19577314-A-G Y77045 YY+
19062250-G-A 16950370-G-A FT237478 YY+
6401744-C-T 6533703-C-T BY60187 +
3025821-C-A 3157780-C-A FT234970 +
3055717-A-G 3187676-A-G FT234978 +
3063138-T-G 3195097-T-G FT144669 +
3309327-C-G 3441286-C-G FT235057 +
3322204-A-G 3454163-A-G FT235059 +
3479699-A-G 3611658-A-G FT235108 +
3695248-T-C 3827207-T-C FT235160 +
4142497-T-C 4274456-T-C FT235278 +
5109820-G-A 5241779-G-A FT235522 +
5192300-A-T 5324259-A-T FT235541 +
5873984-T-A 6005943-T-A FT235724 +
6694123-G-A 6826082-G-A FT235854 Y+
6974891-G-A 7106850-G-A FT235911 YY+
7107597-G-T 7239556-G-T FT235934 YY+
7204279-G-A 7336238-G-A YY+
8976172-T-C 9138563-T-C FT236295 Y+
9385645-G-A 9548036-G-A FT236332 Y+
9644137-G-A 9806528-G-A FT236361 IR3_Prx +
9727364-G-T 9889755-G-T FT236365 IR3_Prx +
10898656-T-C FT435859 +
13666050-T-G 11510374-T-G FT447676 +
13831696-G-A 11710990-G-A FT236404 +
13894739-C-G 11774033-C-G FT236428 Y+
14214579-T-A 12093873-T-A FT236535 YY+
14296317-A-C 12175611-A-C FT236566 YY+
14474967-A-T 12354236-A-T FT236601 YY+
15161283-A-C 13049369-A-C FT236728 YY+
15161284-G-T 13049370-G-T FT236729 YY+
15335422-A-G 13223540-A-G FT236759 YY+
15578339-T-A 13466459-T-A FT236814 YY+
15703894-G-A 13592014-G-A FT236826 YY+
15841126-T-C 13729246-T-C FT236854 YY+
15910687-G-A 13798807-G-A FT236866 YY+
16539265-G-C 14427385-G-C FT236970 YY+
16858619-T-G 14746739-T-G FT237041 YY+
16917367-C-T 14805487-C-T YY+
17150033-C-T 15038153-C-T FT237092 YY+
17343492-G-C 15231612-G-C FT237141 YY+
18391416-T-A 16279536-T-A FT237367 P6_Gap +
18398929-ACTAT-A 16287049-ACTAT-A P6_Gap +
18616167-T-C 16504287-T-C FT237391 YY+
18732955-A-G 16621075-A-G FT237414 YY+
19004702-T-C 16892822-T-C FT237462 YY+
19105451-C-A 16993571-C-A FT237492 YY+
19381848-T-C 17269968-T-C FT237560 YY+
19514959-C-T 17403079-C-T FT237589 YY+
21038131-T-C 18876245-T-C FT237595 Y+
21431508-A-G 19269622-A-G FT237678 YY+
22228926-T-C 20067040-T-C FT453200 DYZ19 +
22437003-G-A 20275117-G-A BY47947 DYZ19 +
22475966-T-C 20314080-T-C FT459811 DYZ19 +
22618285-C-T 20456399-C-T FT237888 YY+
22762851-A-C 20600965-A-C FT237915 YY+
23236003-T-C 21074117-T-C FT238009 Y+
23399142-TC-T 21237256-TC-T +
23465522-C-T 21303636-C-T FT238053 Y+
23761996-C-T 21600110-C-T Y+
24390331-A-G 22244184-A-G FT238139 Y+
24409907-G-A 22263760-G-A FT238150 Y+
22253831-C-T 20091945-C-T DYZ19 *
11011255-G-GCACTC *
22233466-A-G 20071580-A-G DYZ19 *
22298931-G-T 20137045-G-T DYZ19 *
22509475-A-G 20347589-A-G BY165654 DYZ19 **
11003215-TCTCCA-T **
20631072-A-AG 18469186-A-AG P4_Prx **
13347858-C-T 11192182-C-T **
22509481-G-T 20347595-G-T BY165655 DYZ19 **
3327923-A-G 3459882-A-G **
6046244-A-T 6178203-A-T **
8296282-C-G 8428241-C-G **
8296466-A-G 8428425-A-G **
9924836-T-G 10087227-T-G **
14100891-C-T 11980185-C-T **
15380885-A-G 13269005-A-G **
22235971-A-C 20074085-A-C DYZ19 **
22438937-G-A 20277051-G-A DYZ19 **
23601269-G-C 21439383-G-C **
27967434-T-C 25821287-T-C P1_Y2 **
28680422-CATTTATTT-C 26534275-CATTTATTT-C 11×ATTT**
3828580-CAT-C 3960539-CAT-C ***
56841871-C-A ***
4196934-CAA-C,CA 4328893-CAA-C,CA 16×A***
22345975-A-G 20184089-A-G DYZ19 ***
28602523-TTGA-T,TGA 26456376-TTGA-T,TGA ***

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.