Tree Position

R-P312/S116 > Z290 > L21/S145 > S552 > DF13 > Z39589 > Z251/S470 > S11556 > Z17665 > Z17662 > Z18107

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
180639
14328881-G-A 12208175-G-A Y91080 YY+
15421480-A-G 13309600-A-G Y93757 YY+
17236037-A-C 15124157-A-C BY113182 YY+
19141887-G-A 17030007-G-A Y103785 YY+
22439173-A-T 20277287-A-T BY16988 DYZ19 +
22439174-G-T 20277288-G-T FT387253 DYZ19 +
22442141-G-A 20280255-G-A DYZ19 +
24071936-C-T 21925789-C-T BY160807 P3_b1 +
20602012-G-A 18440126-G-A P5_Dst **
2884843-A-G 3016802-A-G PR199 **
5702620-CAAAAAAA-C 5834579-CAAAAAAA-C 25×A**
6757694-A-G 6889653-A-G Z523 **
13860859-GCAATA-G 11740153-GCAATA-G **
15773296-G-A 13661416-G-A CTS4691 **
17559790-G-A 15447910-G-A CTS7605 PF3764 Z2656 **
18232452-C-T 16120572-C-T PF7643 **
58976782-A-C 56830635-A-C **
13810066-AACGTT-A 11689360-AACGTT-A ***
10023652-C-G 10186043-C-G ***
10023654-C-CCA 10186045-C-CCA ***
10023660-GCCTATTTC-G 10186051-GCCTATTTC-G ***
13803212-G-A 11682506-G-A ***
13818090-A-G 11697384-A-G ***
16494396-TAG-T,TAT 14382516-TAG-T,TAT 10×AG***
13818693-G-A 11697987-G-A FTA3208 ***
16345135-CTCTTCT-C,CT 14233255-CTCTTCT-C,CT 18×TCT***
13454954-G-C 11299278-G-C A8492 ***
16292546-A-AT 14180666-A-AT 48×T***
13196165-C-T 11040489-C-T ***
13838280-T-A 11717574-T-A FT146239 ***
13139538-T-C 10629024-T-C ***
13459491-A-G 11303815-A-G ***
13805308-A-C 11684602-A-C ***
10023644-G-T 10186035-G-T ***
13803185-C-T 11682479-C-T ***
13803188-G-A 11682482-G-A ***
20927099-G-GTT 18765213-G-GTT P4_Dst 35×T***
58846063-G-GCATTC 56744796-C-CGGAAT ***
6181331-G-A 6313290-G-A IR3_Dst ***
6347810-GAAAGAGAA-G 6479769-GAAAGAGAA-G ***
6349152-G-A 6481111-G-A FGC8008 Z12225 ***
6863815-C-T 6995774-C-T ***
7053321-C-A 7185280-C-A ***
9030403-G-GGAAAA 9192794-G-GGAAAA ***
10024128-T-C 10186519-T-C ***
13137871-G-C 10627357-G-C ***
13142228-CATACT-C 10631714-CATACT-C ***
13446784-C-T 11291108-C-T ***
13446803-T-C 11291127-T-C ***
13448853-A-C,T 11293177-A-C,T ***
13455016-G-A 11299340-G-A ***
13456115-A-G 11300439-A-G ***
13458186-A-G 11302510-A-G ***
13648111-GAATGT-G 11492435-GAATGT-G ***
13686832-G-A 11531156-G-A ***
13686858-G-C 11531182-G-C ***
13799169-T-TGGAATGGAAC 11678463-T-TGGAATGGAAC ***
13801518-A-T 11680812-A-T ***
13801523-G-A 11680817-G-A FT451639 ***
13801578-G-T 11680872-G-T ***
13803157-C-A 11682451-C-A ***
13803184-T-C 11682478-T-C ***
13804706-T-G 11684000-T-G ***
13808153-A-T 11687447-A-T ***
13813827-G-T 11693121-G-T ***
13813882-G-A 11693176-G-A FGC14117FGC14123 ***
13813890-T-A 11693184-T-A ***
13817773-G-A 11697067-G-A ***
13818060-A-G 11697354-A-G ***
13818128-GAATAA-G,GAATGG 11697422-GAATAA-G,GAATGG ***
13818696-T-A 11697990-T-A ***
13827047-TGGTAA-T 11706341-TGGTAA-T ***
13827057-T-A 11706351-T-A ***
13827478-G-C 11706772-G-C ***
13830179-C-T 11709473-C-T FGC45786 ***
13833862-G-C 11713156-G-C FT67545 ***
13833895-T-TTTAGG 11713189-T-TTTAGG ***
13838251-G-C 11717545-G-C ***
13838275-T-A 11717569-T-A ***
13838276-G-T 11717570-G-T ***
13839929-T-C 11719223-T-C ***
13839930-G-A 11719224-G-A ***
13841931-A-T 11721225-A-T ***
13841955-T-G 11721249-T-G ***
13846514-GGACCAGAATGGATTC-G 11725808-GGACCAGAATGGATTC-G ***
13850595-C-G 11729889-C-G ***
13855117-A-G 11734411-A-G ***
13859327-A-G 11738621-A-G ***
13865873-T-A 11745167-T-A ***
13865908-A-C,T 11745202-A-C,T ***
16108594-T-C 13996714-T-C P8_Prx ***
16108662-A-T 13996782-A-T P8_Prx ***
16118998-CTT-C 14007118-CTT-C P8_Prx 14×T***
16860780-AAAAG-A,AA 14748900-AAAAG-A,AA 9×AAAG***
17037296-G-T 14925416-G-T Z42904 ***
19868177-G-T 17756297-G-T P5_Prx ***
22247020-G-C 20085134-G-C DYZ19 ***
22255828-T-C 20093942-T-C DYZ19 ***
22325298-C-T 20163412-C-T DYZ19 ***
22325365-TG-T 20163479-TG-T DYZ19 ***
22325367-G-C 20163481-G-C DYZ19 ***
25215948-G-A 23069801-G-A P2_r1 ***
25462329-CACAG-C 23316182-CACAG-C P2_r2 4×ACAG***
28311168-GGGAAGGAA-G 26165021-GGGAAGGAA-G P1_b4 12×GGAA***
28784720-CTGTGGAGGGA-C 26638573-CTGTGGAGGGA-C ***
28784809-G-C 26638662-G-C ***
28784815-G-A 26638668-G-A ***
28799819-A-C 26653672-A-C ***
28799855-A-G 26653708-A-G ***
28800284-G-T 26654137-G-T ***
28800287-G-A 26654140-G-A ***
28800301-G-C 26654154-G-C ***
28800302-G-A 26654155-G-A ***
28800306-T-C 26654159-T-C ***
28800339-A-G 26654192-A-G ***
58975536-G-C,T 56829389-G-C,T ***
58979662-T-C 56833515-T-C ***
58979670-G-C 56833523-G-C ***
58981256-G-C,T 56835109-G-C,T ***
58981298-T-C 56835151-T-C ***
13866334-C-A,G 11745628-C-A,G ***
7650849-AC-A,AA 7782808-AC-A,AA ***
13139661-T-A,C 10629147-T-A,C 5×ATTCC***
13856402-T-A,G 11735696-T-A,G ***
23255678-AC-A,AA 21093792-AC-A,AA ***

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.