Tree Position

A0-T-YP2191 > P305[A1] > A1b > BT/A1b2 > M168/PF1416[CT] > P143[CF] > M89/PF2746[F] > F1329/M3658[GHI > F929[HIJK] > IJK > K > M526[K2] > P295[P] > M242[Q] > L472 > L56 > L53 > L54 > M930 > M3 > M884 > Exact position not yet finalized.

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 STR1kG
HG01961
6971660-G-T 7103619-G-T Y22897CTS717 YY+
14315311-G-T 12194605-G-T FT335462 YY+
2861404-G-A 2993363-G-A FT333454 YY+
5130006-A-C 5261965-A-C +
5189735-G-A 5321694-G-A +
5367383-A-G 5499342-A-G +
6473625-G-C 6605584-G-C +
6866757-G-A 6998716-G-A Z35738 YY+
7265739-G-A 7397698-G-A FT333781 YY+
7295296-A-C 7427255-A-C Z35739 YY+
7324637-A-T 7456596-A-T Z35740 YY+
7387744-C-G 7519703-C-G Z35741 YY+
7428534-G-A 7560493-G-A FT333866 YY+
7731398-A-G 7863357-A-G YY+
7903661-T-C 8035620-T-C FT334116 YY+
8212469-T-C 8344428-T-C FT334320 YY+
8300889-A-G 8432848-A-G FT334367 YY+
8845715-A-G 8977674-A-G FT334764 YY+
8970710-A-G 9133101-A-G +
8983795-C-T 9146186-C-T FTB21215 +
8986276-A-G 9148667-A-G +
9381292-C-T 9543683-C-T Y+
9804602-T-C 9966993-T-C FT334993 Y+
9915046-T-C 10077437-T-C Y+
10094470-C-T 10256861-C-T +
13248096-G-T 11092420-G-T +
13330318-A-G 11174642-A-G +
13453678-C-T 11298002-C-T F18157 +
13563812-C-T 11408136-C-T +
13668320-C-T 11512644-C-T +
14010826-C-T 11890120-C-T FT328992 YY+
14141629-A-T 12020923-A-T FT335296 YY+
14193905-G-A 12073199-G-A Y66146 YY+
14216371-G-A 12095665-G-A FT335367 YY+
14291708-G-C 12171002-G-C FT335438 Y+
14298968-G-A 12178262-G-A FT335443 YY+
14397974-G-A 12277270-G-A FT335529 Y+
14541808-G-A 12430009-G-A FT335634 YY+
14948141-A-G 12836215-A-G YY+
15194848-T-G 13082934-T-G FT335995 YY+
15460447-C-T 13348567-C-T FT336170 YY+
15688461-C-T 13576581-C-T YY+
15757834-G-T 13645954-G-T Y51107 YY+
16198054-G-A 14086174-G-A FT336610 YY+
16318423-G-A 14206543-G-A FT336702 Y+
16496839-A-G 14384959-A-G Y96513 YY+
16608845-A-T 14496965-A-T YY+
17150583-A-G 15038703-A-G FT337245 YY+
17268539-C-T 15156659-C-T Y+
17318386-G-A 15206506-G-A FT337347 YY+
17451911-A-G 15340031-A-G FT337446 Y+
17594676-G-A 15482796-G-A FT337542 YY+
17794910-A-G 15683030-A-G FT337695 YY+
18381954-A-G 16270074-A-G FT338025 P6_Gap +
18684433-A-G 16572553-A-G FT338187 YY+
19297810-G-A 17185930-G-A FT111953 Y+
19473177-T-G 17361297-T-G FT338779 YY+
20533309-C-T 18371423-C-T P5_Dst +
21212253-C-T 19050367-C-T FT338964 YY+
21873474-G-A 19711588-G-A FT339463 YY+
21947467-G-T 19785581-G-T FT339516 YY+
21953812-G-A 19791926-G-A FT339522 YY+
22218054-T-C 20056168-T-C DYZ19 +
22287831-T-C 20125945-T-C DYZ19 +
22445735-T-C 20283849-T-C BY219698 DYZ19 +
22462333-G-A 20300447-G-A FT421629 DYZ19 +
22471940-T-G 20310054-T-G DYZ19 +
22596735-G-T 20434849-G-T FT339762 YY+
22885414-T-C 20723528-T-C FT339948 YY+
23384022-C-G 21222136-C-G YY+
23536187-A-G 21374301-A-G FT340390 YY+
23754765-C-G 21592879-C-G FT340467 Y+
23784715-C-G 21622829-C-G FT340488 Y+
28472855-G-T 26326708-G-T FT340642 +
28737691-T-C 26591544-T-C +
28803416-C-G 26657269-C-G +

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.