Tree Position

R-P312/S116 > Z40481 > ZZ11 > U152/S28 > L2/S139 > DF110 > BY42653

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
17956510-T-A 15844630-T-A Y53999 YY+
8537119-G-C 8669078-G-C Y47499 YY+
21562790-C-A 19400904-C-A BY411M2268 Y539 S23267 Z4948 ZS12558 YY+
17853930-ATAGT-A 15742050-ATAGT-A +
16936270-C-T 14824390-C-T Y52558 YY+
16929013-C-T 14817133-C-T Y52549 FGC74753 YY+
16585217-C-T 14473337-C-T Y52077 YY+
16301452-A-G 14189572-A-G Y51679 YY+
16211400-C-T 14099520-C-T Y51512 YY+
18777432-G-A 16665552-G-A BY197114FGC75607 Y54887 YY+
14083712-G-A 11963006-G-A Y48970 YY+
13973480-C-A 11852774-C-A BY92018 YY+
19341398-A-C 17229518-A-C Y55739 YY+
13832618-G-A 11711912-G-A Y48728 +
9973819-T-C 10136210-T-C BY53961 Y+
21218670-A-G 19056784-A-G Y56342 YY+
7944031-A-G 8075990-A-G Y46648 YY+
18404347-G-C 16292467-G-C Y54546 P6_Gap +
22741023-G-C 20579137-G-C Y58221 YY+
24454412-A-G 22308265-A-G Y59838 Y+
23767670-G-A 21605784-G-A Y59532 Y+
17506937-C-T 15395057-C-T CTS7491 YY+
23199405-C-A 21037519-C-A BY55437 Y+
23070213-T-A 20908327-T-A Y58687 YY+
23070212-C-A 20908326-C-A Y58686 YY+
18070845-C-T 15958965-C-T Y54175 YY+
7414655-G-A 7546614-G-A Y46014 YY+
22471192-T-G 20309306-T-G DYZ19 +
22097998-C-A 19936112-C-A Y57624 YY+
21673032-A-C 19511146-A-C Y57053 YY+
7323724-G-A 7455683-G-A Y45904 YY+
21668275-A-G 19506389-A-G Y57052 YY+
22487701-G-A 20325815-G-A BY225026 DYZ19 **
22487703-G-T 20325817-G-T FT460605 DYZ19 **
27863669-G-A 25717522-G-A BY186170 P1_Y2 **
15790691-C-A 13678811-C-A Y51147 **
22487707-T-G 20325821-T-G BY225028 DYZ19 **
7340005-G-A 7471964-G-A Y45927 **
22473139-G-A 20311253-G-A DYZ19 **
22471173-A-T 20309287-A-T DYZ19 **
22471170-C-A 20309284-C-A DYZ19 **
26326033-C-T 24179886-C-T BY226768 P1_Y1 ***
26107686-TA-T 23961539-TA-T P1_Y1 ***
25704696-T-C 23558549-T-C P1_b3 ***
25162566-G-A 23016419-G-A g1 ***
24815188-C-T 22669041-C-T P3_b2 ***
24279000-A-C 22132853-A-C P3_t1 ***
24090572-G-T 21944425-G-T P3_b1 ***
13857556-G-C 11736850-G-C ***
22473124-C-T 20311238-C-T Y2903 FGC10161 DYZ19 ***
22487919-G-A 20326033-G-A BY168977 DYZ19 ***
9329195-A-C 9491586-A-C ***
22487746-G-T 20325860-G-T DYZ19 ***
13859828-C-G 11739122-C-G ***
22487747-T-C 20325861-T-C DYZ19 ***
22313340-T-G 20151454-T-G DYZ19 ***
22296723-A-T 20134837-A-T DYZ19 ***
22280338-A-T 20118452-A-T DYZ19 ***
22222489-G-C 20060603-G-C DYZ19 ***
58978364-T-C 56832217-T-C ***
9220355-C-T 9382746-C-T ***
20628011-C-T 18466125-C-T P4_Prx ***
19436740-G-GAAAGAA 17324860-G-GAAAGAA ***

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: N1287371062153576702917743884
Used in age calculations1062153576702917743884
Counts of SNPs2626
Variant counts last updated 2022-08-28 03:21:18.

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