Tree Position

R-P312/S116 > Z290 > L21/S145 > S552 > DF13

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
26053538-T-G 23907391-T-G P1_Y1 4×TTTGA+
21748436-A-G A+
4774340-T-A 4906299-T-A A+
18528154-T-C 16416274-T-C P6_Dst A+
20634474-G-T 18472588-G-T P4_Prx A+
25548054-T-C 23401907-T-C P1_gr1 A+
58980032-C-T 56833885-C-T A*
10946525-C-A A*
56827512-C-T A*
56833080-C-T A*
56835681-T-A A*
56832338-T-C A*
56832324-C-G A*
6334295-G-A 6466254-G-A IR3_Dst A*
13687253-G-T 11531577-G-T A*
18280953-A-G 16169073-A-G P6_Prx A*
18294162-T-G 16182282-T-G P6_Prx A*
18984953-T-TC 16873073-T-TC A*
19781701-G-A 17669821-G-A P5_Prx A*
19880863-G-C 17768983-G-C P5_Prx A*
20750542-G-A 18588656-G-A P4_Prx A*
22256952-G-C 20095066-G-C DYZ19 A*
22265095-G-T 20103209-G-T DYZ19 A*
24270529-A-G 22124382-A-G P3_b1 A*
56833412-T-C A*
16595426-A-G 14483546-A-G TCTS5987 YY+
5275721-A-G 5407680-A-G BY21628FGC7777 YFS032832 +
7371741-C-T 7503700-C-T FT310682 Y+
8531883-C-T 8663842-C-T FT226394 YY+
23778851-A-G 21616965-A-G BY13882BY13886 Y+
11005659-C-A +
3249166-T-A 3381125-T-A FTA42388 +
3418943-A-C 3550902-A-C FTA42425 +
3553988-A-G 3685947-A-G FTA42453 +
3558090-T-C 3690049-T-C FTA42454 +
3565052-G-C 3697011-G-C FTA21160 +
4336368-C-T 4468327-C-T FTA42654 +
4733511-C-T 4865470-C-T FTA42738 +
4837777-C-T 4969736-C-T FTA42760 +
5047487-A-G 5179446-A-G FTA42812 +
5164285-A-C 5296244-A-C FTA42832 +
5275716-A-T 5407675-A-T FTA42855 +
5988558-G-C 6120517-G-C FTA43046 +
6057205-G-T 6189164-G-T FTA43071 +
7062861-G-C 7194820-G-C FTA35871 Y+
7312276-T-A 7444235-T-A FTA35904 YY+
8192627-C-G 8324586-C-G FTA36007 YY+
8342395-G-C 8474354-G-C FTA36024 YY+
9846909-G-A 10009300-G-A FTA36139 YY+
9995710-A-G 10158101-A-G Y+
10048478-T-G 10210869-T-G +
10809147-C-T +
13693753-G-T 11538077-G-T +
14660137-TTGGC-T 12548202-TTGGC-T +
15713417-T-G 13601537-T-G FTA36379 YY+
15896258-G-A 13784378-G-A YY+
16270202-A-T 14158322-A-T FTA36437 YY+
17399768-G-C 15287888-G-C FTA36573 YY+
17537662-C-G 15425782-C-G FTA36589 YY+
18063965-T-G 15952085-T-G FTA36654 YY+
18549908-G-A 16438028-G-A FTA36698 Y+
18655836-C-T 16543956-C-T FTA36712 YY+
18987667-C-A 16875787-C-A FTA36758 Y+
21210462-T-G 19048576-T-G FTA36875 YY+
21252282-C-T 19090396-C-T FTA36881 YY+
21327076-C-T 19165190-C-T FTA36901 YY+
21494399-A-T 19332513-A-T FTA36931 YY+
21620805-C-T 19458919-C-T FTA36953 YY+
21760451-G-A 19598565-G-A FTA36969 YY+
21770373-G-A 19608487-G-A FTA36972 Y+
21836258-C-T 19674372-C-T FTA36982 Y+
22091928-T-C 19930042-T-C FTA37011 YY+
23118541-G-A 20956655-G-A YY+
23868737-C-T 21706851-C-T FTA37178 Y+
26092143-A-C 23945996-A-C P1_Y1 +
28484667-C-T 26338520-C-T FTA37198 +
28604566-T-C 26458419-T-C FTA37212 +
28607304-A-G 26461157-A-G FTA37213 +
18600-G-T +
13213751-C-CATGG 11058075-C-CATGG 9×ATGG*
6402351-C-T 6534310-C-T Y5541 Z20113 *
10883895-CCCATT-C *
10796723-G-A FT431603 *
22299066-G-A 20137180-G-A BY216731 DYZ19 *
22281628-G-T 20119742-G-T BY216050 DYZ19 *
22315803-C-G 20153917-C-G DYZ19 *
22317161-C-A 20155275-C-A DYZ19 *
22319618-G-C 20157732-G-C DYZ19 *
26248213-G-T 24102066-G-T P1_Y1 **
22485979-A-T 20324093-A-T DYZ19 **
14613459-CTTTT-C 12501657-CTTTT-C 26×T**
24270881-A-T 22124734-A-T P3_b1 **
10961466-C-T **
5883475-A-C 6015434-A-C **
6007764-A-G 6139723-A-G **
6451544-T-C 6583503-T-C **
8826372-T-TA 8958331-T-TA **
10961464-A-AAT **
13293975-A-G 11138299-A-G **
14132931-G-A 12012225-G-A **
14961145-T-C 12849220-T-C **
15893211-G-A 13781331-G-A **
16653088-A-G 14541208-A-G **
16726589-T-C 14614709-T-C **
17017281-T-G 14905401-T-G **
17330289-T-C 15218409-T-C **
17727286-T-C 15615406-T-C **
18261838-A-T 16149958-A-T **
18540750-A-G 16428870-A-G **
22788919-T-C 20627033-T-C **
24270885-A-T 22124738-A-T P3_b1 **
24612840-ATTT-A 22466693-ATTT-A P3_t2 16×T**
25305259-T-C 23159112-T-C P2_r1 **
27503315-C-G 25357168-C-G P1_Y2 **
28396076-A-AG 26249929-A-AG P1_gr2 **
6419046-A-ATGTG 6551005-A-ATGTG 18×TG***
17520309-CA-C 15408429-CA-C 9×A***
10660117-TTTCCA-T ***
8085456-A-G 8217415-A-G ***
6467392-CTT-C,CT 6599351-CTT-C,CT 15×T***
3957629-T-A 4089588-T-A 7×AAATA***
10796718-ATTCCG-A ***
21966549-GT-G,GTT 19804663-GT-G,GTT 16×T***
3548670-AT-A,ATT 3680629-AT-A,ATT 17×T***
6128714-C-T 6260673-C-T ***
7345934-T-C 7477893-T-C ***
10015048-C-G 10177439-C-G ***
14727015-T-C 12615083-T-C ***
15143486-A-T 13031573-A-T ***
15815472-G-A 13703592-G-A ***
16046631-TACACAC-T 13934751-TACACAC-T 17×AC***
18702050-G-T 16590170-G-T ***
23051606-A-G 20889720-A-G ***
23440972-A-G 21279086-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.