Tree Position

R-P312/S116 > Z40481 > ZZ11 > DF27/S250 > ZZ12 > BY70330

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
N17543
27637376-C-T 25491229-C-T P1_Y2 A+
24306193-G-A 22160046-G-A P3_t1 A*
28816614-G-T 26670467-G-T A*
16570494-T-TTA 14458614-T-TTA A*
16570508-T-A 14458628-T-A YYA*
19581314-G-A 17469434-G-A P5_Prx YA*
22232141-A-G 20070255-A-G DYZ19 A*
26325063-G-A 24178916-G-A P1_Y1 A*
28817647-A-C 26671500-A-C 9×GGAATA*
23046480-C-T 20884594-C-T BY2709BY2709 YY+
4663293-A-T 4795252-A-T FT2562 +
5240768-T-C 5372727-T-C FT2626 +
17033889-C-T 14922009-C-T Y56 YY+
23804428-T-C 21642542-T-C Y19043 Y+
18392024-G-A 16280144-G-A Y54522 P6_Gap +
3675636-G-A 3807595-G-A FT2477 +
4507896-G-T 4639855-G-T FT2552 +
4685762-C-A 4817721-C-A FT2566 +
4805199-A-G 4937158-A-G FT2576 +
5042770-A-G 5174729-A-G FT2614 +
6099592-C-G 6231551-C-G FT2707 +
6428772-T-G 6560731-T-G FT2718 +
6854140-A-G 6986099-A-G FT2738 YY+
7411383-G-A 7543342-G-A FT2764 YY+
7645465-G-A 7777424-G-A FT2775 YY+
8212698-C-T 8344657-C-T FT2809 YY+
9787211-G-T 9949602-G-T FT2851 Y+
10858268-G-A FT434317 +
14201233-T-C 12080527-T-C FT2898 YY+
14365280-G-A 12244575-G-A FT2910 YY+
14370741-G-A 12250037-G-A YY+
14408020-C-T 12287318-C-T FT2912 YY+
14850795-A-C 12738861-A-C FT2931 YY+
15166890-C-T 13054976-C-T FT2947 YY+
15286346-A-G 13174445-A-G FT2952 Y+
15484809-CT-C 13372929-CT-C +
15553918-A-T 13442038-A-T FT2966 YY+
16260647-G-T 14148767-G-T FT3002 YY+
16274361-C-T 14162481-C-T FT3003 YY+
16817227-C-A 14705347-C-A FT3028 YY+
16926569-T-G 14814689-T-G FT3035 Y+
17451851-C-T 15339971-C-T FT3062 Y+
18046495-G-T 15934615-G-T FT3088 YY+
19415513-G-A 17303633-G-A FT3144 YY+
21702523-C-T 19540637-C-T FT3189 YY+
23028477-T-G 20866591-T-G FT3241 Y+
23508885-C-A 21346999-C-A FT3262 YY+
23617060-C-T 21455174-C-T FT3263 YY+
28814161-G-T 26668014-G-T FT462714 +
22304211-G-T 20142325-G-T BY200506 DYZ19 *
18641965-CAA-C,CA 16530085-CAA-C,CA 13×A*
5442529-T-TA 5574488-T-TA 10×A*
22317580-T-A 20155694-T-A DYZ19 *
4734556-G-A 4866515-G-A Y4430 FGC3606 **
21570005-G-A 19408119-G-A FT182165 **
17669702-T-C 15557822-T-C **
5220159-CTTTTT-C 5352118-CTTTTT-C 21×T**
2984717-TA-T 3116676-TA-T **
2984721-TA-T 3116680-TA-T **
5355237-T-G 5487196-T-G **
5883926-C-G 6015885-C-G **
5947344-G-A 6079303-G-A FT114802 **
17219726-T-C 15107846-T-C **
27516153-A-G 25370006-A-G P1_Y2 **
7199235-AT-A 7331194-AT-A 9×T***
5495445-G-GTT 5627404-G-GTT 14×T***
3745023-G-GT 3876982-G-GT ***
6955236-G-A 7087195-G-A ***
9697146-TTGTGTGTG-T,TTG 9859537-TTGTGTGTG-T,TTG IR3_Prx 18×TG***
13540253-AACACACAC-A,AACAC 11384577-AACACACAC-A,AACAC 23×AC***
13699020-T-A 11543344-T-A ***
14219714-CA-C,CAA 12099008-CA-C,CAA 14×A***
14570756-ATT-A,ATTT 12458956-ATT-A,ATTT 22×T***
17648536-ATTT-A,ATT 15536656-ATTT-A,ATT 22×T***
18628964-CA-C 16517084-CA-C ***
19138084-CTATATA-C 17026204-CTATATA-C 10×TA***
19250661-T-G 17138781-T-G ***
19376298-GC-G 17264418-GC-G ***
19376306-A-G 17264426-A-G ***
19376307-T-C 17264427-T-C ***
22278798-G-C 20116912-G-C DYZ19 ***
23427003-G-A 21265117-G-A ***

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.