Tree Position

R-P312/S116 > Z290 > L21/S145 > S552 > DF13 > FGC11134

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
2686256-CTATG-C 2818215-CTATG-C +
2804221-AGGC-A 2936180-AGGC-A +
7057768-C-T 7189727-C-T BY63105 YY+
8011799-C-T 8143758-C-T YY+
8441865-T-C 8573824-T-C BY72795 YY+
8881930-G-A 9013889-G-A BY76601 Y+
9031421-T-A 9193812-T-A BY53862 Y+
9131094-T-C 9293485-T-C F1493 M6377 Y+
9380422-A-AG 9542813-A-AG +
9848456-CAT-C 10010847-CAT-C +
13714655-G-A 11558979-G-A +
13900023-A-C 11779317-A-C YY+
14248623-A-C 12127917-A-C BY94326 YY+
14581865-G-T 12470065-G-T YY+
15224122-T-G 13112208-T-G BY100256 Y+
15228221-G-C 13116307-G-C BY100314 Y+
15439808-C-A 13327928-C-A BY101585 YY+
15950767-G-A 13838887-G-A BY105095 YY+
15967221-T-C 13855341-T-C BY105181 YY+
16385627-G-A 14273747-G-A BY107400 YY+
16551965-A-C 14440085-A-C BY108554 YY+
16877458-C-G 14765578-C-G BY110799 YY+
17772993-C-T 15661113-C-T BY117328 YY+
17791065-C-T 15679185-C-T BY117403 YY+
17866254-TCA-T 15754374-TCA-T +
17911727-C-A 15799847-C-A BY118375 YY+
18123740-G-C 16011860-G-C BY120264 YY+
19365275-T-A 17253395-T-A FT306016 YY+
21176789-A-T 19014903-A-T BY130891 YY+
21187027-CT-C 19025141-CT-C +
21223847-C-T 19061961-C-T BY131229 YY+
21481619-C-T 19319733-C-T BY133249 YY+
21519170-A-G 19357284-A-G BY133559 YY+
21610222-C-T 19448336-C-T PR3302 YY+
23655333-T-A 21493447-T-A BY147119 Y+
24493217-C-G 22347070-C-G BY150326 +
26054314-C-T 23908167-C-T BY2439 P1_Y1 +
7164456-A-C 7296415-A-C CTS1038 PF4645 **
19239694-C-T 17127814-C-T FT283456 **
19239695-C-T 17127815-C-T BY127589 **
22369181-T-C 20207295-T-C DYZ19 **
24673352-A-G 22527205-A-G P3_b2 ***
18454935-A-C 16343055-A-C P6_Dst 4×TTTC***
28204103-G-T 26057956-G-T P1_b4 ***
18454938-TC-T 16343058-TC-T P6_Dst ***
13138425-T-C 10627911-T-C ***
20231508-CAAGA-C 18069622-CAAGA-C P5_Dst 21×AAGA***
22337943-A-G 20176057-A-G DYZ19 ***
14025988-G-GAGAAAGAA 11905282-G-GAGAAAGAA 13×AGAA***
13669556-T-C 11513880-T-C ***
16119959-T-TTTTCTTTC 14008079-T-TTTTCTTTC P8_Prx 12×TTTC***
20206684-GA-G 18044798-GA-G P5_Dst 9×A***
27790905-AT-A 25644758-AT-A P1_Y2 10×T***
14026044-G-A 11905338-G-A BY173625 ***
13257877-G-A 11102201-G-A ***
13448906-C-T 11293230-C-T ***
18454860-T-C 16342980-T-C P6_Dst ***
27968354-CT-C 25822207-CT-C P1_Y2 14×T***
6251155-C-G 6383114-C-G IR3_Dst ***
6263519-A-T 6395478-A-T IR3_Dst ***
9178978-G-T 9341369-G-T ***
9519801-T-G 9682192-T-G PF3202Y17271 ***
13809814-G-A 11689108-G-A FT260243 ***
13809822-T-A 11689116-T-A ***
13816627-G-GAAT 11695921-G-GAAT 8×GGAAT***
18297495-G-A 16185615-G-A P6_Prx ***
19705378-C-T 17593498-C-T P5_Prx ***
19733004-C-T 17621124-C-T P5_Prx ***
20022712-T-C 17910832-T-C P5_Prx ***
20641077-A-G 18479191-A-G P4_Prx ***
20659867-G-A 18497981-G-A P4_Prx ***
22221244-C-A 20059358-C-A DYZ19 ***
22249072-C-T 20087186-C-T DYZ19 ***
22259176-T-G 20097290-T-G DYZ19 ***
22264487-C-A 20102601-C-A DYZ19 ***
22280928-T-A 20119042-T-A DYZ19 ***
22290126-G-C 20128240-G-C DYZ19 ***
22315809-T-C 20153923-T-C DYZ19 ***
22366056-T-C 20204170-T-C DYZ19 ***
22428941-T-C 20267055-T-C DYZ19 ***
22453883-G-A 20291997-G-A DYZ19 ***
22477707-C-T 20315821-C-T BY44019 DYZ19 ***
23180098-C-G 21018212-C-G ***
24070778-T-C 21924631-T-C P3_b1 9×AC***
24176843-T-C 22030696-T-C P3_b1 ***
24931126-G-A 22784979-G-A g1 ***
24942294-G-A 22796147-G-A g1 ***
24944147-C-T 22798000-C-T g1 ***
24957217-G-A 22811070-G-A g1 ***
24991045-C-T 22844898-C-T g1 ***
25143478-C-T 22997331-C-T g1 ***
25199098-G-T 23052951-G-T g1 ***
25845104-G-A 23698957-G-A P1_b3 ***
25940180-G-A 23794033-G-A P1_Y1 ***
26080374-C-T 23934227-C-T P1_Y1 ***
26081703-G-T 23935556-G-T P1_Y1 ***
26196064-T-G 24049917-T-G P1_Y1 ***
26421398-C-T 24275251-C-T P1_Y1 ***
26727418-C-A 24581271-C-A P1_g2 ***
27990530-A-C 25844383-A-C P1_Y2 ***
27990535-G-T 25844388-G-T P1_Y2 ***
58820584-C-T 56770287-G-A ***
6226044-CTTCT-C 6358003-CTTCT-C IR3_Dst 13×TTCT***
10019471-A-AAGAGAG 10181862-A-AAGAGAG ***
13816625-A-AGG 11695919-A-AGG ***
18454935-AT-A 16343055-AT-A P6_Dst 4×TTTC***
20951194-AT-A 18789308-AT-A P4_Dst 19×T***
25207634-T-TA 23061487-T-TA P2_r1 ***
26222511-CT-C 24076364-CT-C P1_Y1 10×T***

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.