Tree Position

R-P312/S116 > Z290 > L21/S145 > S552 > DF13 > DF21/S192 > S5488 > BY12129

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
21307406-A-AT 19145520-A-AT +
8134033-A-G 8265992-A-G BY70220 YY+
8760646-C-T 8892605-C-T YY+
8801403-G-C 8933362-G-C BY76001 YY+
9097625-T-C 9260016-T-C BY78049 Y+
9109337-C-T 9271728-C-T BY78176 Y+
13210734-TG-T 11055058-TG-T +
14070595-CAT-C 11949889-CAT-C +
14917854-A-T 12805921-A-T BY98476 YY+
15007821-C-T 12895906-C-T BY99046 YY+
15206997-C-A 13095083-C-A BY100184 YY+
15307782-C-T 13195884-C-T BY100714 YY+
15897590-C-T 13785710-C-T BY104781 YY+
15931028-C-T 13819148-C-T BY104963 YY+
15985347-G-C 13873467-G-C FT180563 YY+
16244522-G-C 14132642-G-C BY106297 YY+
16481998-A-C 14370118-A-C BY108102 YY+
17018529-A-G 14906649-A-G BY111779 YY+
17108836-T-A 14996956-T-A BY112350 YY+
17510866-C-T 15398986-C-T BY115349 YY+
17592271-A-G 15480391-A-G BY115976 YY+
18398454-AATG-A 16286574-AATG-A P6_Gap +
18973951-C-T 16862071-C-T BY125183 YY+
19033349-A-T 16921469-A-T BY125638 YY+
19254692-T-G 17142812-T-G BY127693 YY+
21283587-C-G 19121701-C-G BY131624 YY+
21665085-A-T 19503199-A-T BY134611 YY+
21756930-T-C 19595044-T-C BY135225 YY+
22246246-G-A 20084360-G-A DYZ19 +
22256388-T-A 20094502-T-A BY214389 DYZ19 +
22271186-T-C 20109300-T-C BY215149 DYZ19 +
22364221-G-A 20202335-G-A DYZ19 +
22473553-G-T 20311667-G-T BY222942 DYZ19 +
23001649-ATTG-A 20839763-ATTG-A +
23607543-A-C 21445657-A-C BY45826 YY+
23643487-C-T 21481601-C-T BY147011 Y+
23697749-G-A 21535863-G-A +
23759808-C-T 21597922-C-T BY147482 Y+
28534152-G-T 26388005-G-T BY150652 Y+
16063243-TTTTC-T 13951363-TTTTC-T 4×TTTC**
14256872-G-A 12136166-G-A **
13212409-C-T 11056733-C-T BY84488 **
15677858-A-G 13565978-A-G BY103266 **
18185863-G-T 16073983-G-T **
24868142-C-A 22721995-C-A IR1_R **
13487267-T-A 11331591-T-A ***
13410227-C-T 11254551-C-T ***
22301201-G-T 20139315-G-T DYZ19 ***
25257697-C-T 23111550-C-T P2_r1 ***
22240382-C-A 20078496-C-A DYZ19 ***
22303077-C-A 20141191-C-A BY46625 DYZ19 ***
21906948-CT-C 19745062-CT-C 10×T***
15658259-TAC-T,TAT 13546379-TAC-T,TAT 11×AC***
6141188-C-T 6273147-C-T IR3_Dst ***
20051044-A-G 17939164-A-G P5_Prx ***
20635565-A-G 18473679-A-G P4_Prx ***
20751282-G-C 18589396-G-C P4_Prx ***
20763519-A-G 18601633-A-G P4_Prx ***
22220734-C-A 20058848-C-A DYZ19 ***
22231133-G-C 20069247-G-C FGC18417 DYZ19 ***
22240384-C-A 20078498-C-A DYZ19 ***
22252297-A-C 20090411-A-C DYZ19 ***
22257570-G-A 20095684-G-A BY214501 DYZ19 ***
22279961-A-T 20118075-A-T DYZ19 ***
22509810-T-C 20347924-T-C BY53392 DYZ19 ***
23011080-CT-C 20849194-CT-C ***
24820060-T-A 22673913-T-A P3_b2 ***
25150150-A-T 23004003-A-T g1 ***
25179442-G-A 23033295-G-A g1 ***
26078557-A-C 23932410-A-C P1_Y1 ***
26166702-T-C 24020555-T-C P1_Y1 ***
26225251-G-A 24079104-G-A P1_Y1 ***
28806730-T-C 26660583-T-C ***

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.