Tree Position

R-P312/S116 > Z290 > L21/S145 > DF13 > Z39589 > Z251/S470 > S11556 > S9294 > BY3229 > BY3231 > BY43237 > FGC11986 > FT15187

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
4563080-C-T 4695039-C-T A+
19714259-G-C 17602379-G-C P5_Prx A*
26167479-C-G 24021332-C-G P1_Y1 A*
25985220-C-T 23839073-C-T P1_Y1 A*
25902465-C-A 23756318-C-A P1_Y1 A*
25540513-T-C 23394366-T-C P1_gr1 A*
13687780-T-C 11532104-T-C A*
26332349-G-A 24186202-G-A P1_Y1 A*
20792279-C-A 18630393-C-A P4_Prx A*
19413311-CTT-C 17301431-CTT-C +
8481907-A-G 8613866-A-G FT212126 YY+
8089758-T-A 8221717-T-A FT124971 YY+
7168972-A-G 7300931-A-G FT124933 YY+
8046800-T-A 8178759-T-A FT212051 YY+
7387037-G-A 7518996-G-A FT124946 YY+
19220402-T-G 17108522-T-G FT213276 YY+
6398544-T-C 6530503-T-C FT211777 +
19441802-C-T 17329922-C-T FT125241 YY+
5937638-A-T 6069597-A-T FT211717 +
8653771-G-A 8785730-G-A FT212166 YY+
8898659-A-T 9030618-A-T BY76764 Y+
19068276-C-T 16956396-C-T FT125224 YY+
10070413-C-T 10232804-C-T FT427239 +
18963317-A-G 16851437-A-G FT125220 YY+
5377172-T-G 5509131-T-G FT211608 +
18936156-C-T 16824276-C-T FT213232 YY+
18910426-G-A 16798546-G-A FT213227 YY+
13689109-C-A 11533433-C-A FT448528 +
18740432-G-A 16628552-G-A FT213193 YY+
13952667-T-G 11831961-T-G FT212361 Y+
14349985-C-G 12229280-C-G FT125062 YY+
18232562-C-G 16120682-C-G FT213135 Y+
14884483-G-C 12772549-G-C FT125083 YY+
17595961-G-C 15484081-G-C FT213031 YY+
15400793-T-C 13288913-T-C FT212632 Y+
15918322-G-A 13806442-G-A FT125111 YY+
5451405-G-A 5583364-G-A FT211624 +
11024507-C-T FT219170 +
5127381-T-C 5259340-T-C FT211555 +
21889497-T-C 19727611-T-C FT213508 YY+
28644717-G-A 26498570-G-A FT103427 +
24450487-C-A 22304340-C-A FT125360 Y+
24445363-C-T 22299216-C-T FT213796 Y+
23794166-A-G 21632280-A-G FT213754 Y+
23157378-G-T 20995492-G-T FT213670 Y+
23046744-T-C 20884858-T-C FT213639 YY+
22734196-C-T 20572310-C-T FT213590 YY+
22460098-T-G 20298212-T-G FT219171 DYZ19 +
22203569-T-C 20041683-T-C FT213556 YY+
2810055-C-T 2942014-C-T FT211074 YY+
3555730-A-G 3687689-A-G FT211206 +
5048516-A-G 5180475-A-G FT124845 +
4579882-T-C 4711841-T-C FT211448 +
16556584-C-T 14444704-C-T FT125134 YY+
3948361-A-G 4080320-A-G FT211296 +
3881473-G-A 4013432-G-A FT211278 +
17332474-G-C 15220594-G-C FT212971 YY+
2826245-C-T 2958204-C-T FT211076 YY+
3388187-G-A 3520146-G-A *
21860905-C-CA 19699019-C-CA *
10657262-CTCCATTCCAT-C *
22967779-C-CA 20805893-C-CA 8×A*
22538058-C-T 20376172-C-T **
22753654-AAC-A 20591768-AAC-A **
22833516-G-T 20671630-G-T **
21076524-G-T 18914638-G-T **
20632773-G-T 18470887-G-T P4_Prx **
23226378-A-G 21064492-A-G **
20632780-G-T 18470894-G-T P4_Prx **
17643483-T-C 15531603-T-C **
23009741-G-A 20847855-G-A **
14739804-G-T 12627872-G-T 13×T**
16382379-C-A 14270499-C-A **
4285902-A-T 4417861-A-T **
22297994-G-C 20136108-G-C BY51682 DYZ19 **
13453270-A-T 11297594-A-T **
13453352-T-C 11297676-T-C **
6106085-C-A 6238044-C-A **
21499012-T-G 19337126-T-G **
21393267-A-G 19231381-A-G **
13453255-A-G 11297579-A-G **
22486444-C-A 20324558-C-A DYZ19 **
13453275-A-C 11297599-A-C **
2795663-T-C 2927622-T-C **
28652229-A-T 26506082-A-T FT125372 **
6029446-T-C 6161405-T-C **
10802332-T-A **
16148509-T-TC 14036629-T-TC P8_Dst **
15185899-C-T 13073985-C-T **
14594281-T-C 12482481-T-C **
13707035-A-G 11551359-A-G **
13455826-T-A 11300150-T-A **
9887944-G-A 10050335-G-A **
8058486-G-A 8190445-G-A **
21196874-T-C 19034988-T-C ***
5785700-A-C 5917659-A-C ***
13346071-CA-C 11190395-CA-C 18×A***
5209997-CAAA-C,CAA 5341956-CAAA-C,CAA 16×A***
3452390-C-T 3584349-C-T ***
2707975-GTTT-G,GTTTT 2839934-GTTT-G,GTTTT 18×T***
14514126-A-G 12402331-A-G ***
16786166-T-C 14674286-T-C ***
13466532-A-AT 11310856-A-AT ***
27862535-TGAGA-T,TGAGAGA 25716388-TGAGA-T,TGAGAGA P1_Y2 22×GA***
17074182-C-A 14962302-C-A ***
13488839-CGGT-C,CGGA 11333163-CGGT-C,CGGA ***
13466520-A-T 11310844-A-T ***
5878150-CT-C,CTT 6010109-CT-C,CTT 14×T***
5742075-TA-T 5874034-TA-T 10×A***
21177129-T-C 19015243-T-C ***
9645653-CTTT-C,CT 9808044-CTTT-C,CT IR3_Prx 20×T***
10041502-A-G 10203893-A-G ***
22193111-C-T 20031225-C-T ***
4008588-CA-C 4140547-CA-C 10×A***
13470791-T-A 11315115-T-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.

Age Analysis Information (work in progress)

Kit: 3195491475665492598038242538
Used in age calculations1475665492598038242538
Counts of SNPs2830
Variant counts last updated 2021-02-13 03:09:08.

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