Tree Position

R-P312/S116 > Z290 > L21/S145 > S552 > DF13 > Z39589 > S1051

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
IN68097
9617499-C-T 9779890-C-T IR3_Prx A+
6252872-G-A 6384831-G-A IR3_Dst A*
28817638-G-T 26671491-G-T A*
19739064-C-T 17627184-C-T P5_Prx A*
6167385-T-C 6299344-T-C IR3_Dst A*
6305199-G-A 6437158-G-A IR3_Dst A*
6324338-G-A 6456297-G-A IR3_Dst A*
20778541-C-T 18616655-C-T P4_Prx A*
22232445-A-G 20070559-A-G DYZ19 A*
22276713-A-G 20114827-A-G DYZ19 A*
24305787-T-C 22159640-T-C P3_t1 A*
25887050-C-T 23740903-C-T P1_Y1 A*
26295957-G-A 24149810-G-A P1_Y1 A*
26352201-C-T 24206054-C-T P1_Y1 A*
26517797-G-A 24371650-G-A P1_Y1 A*
28817639-G-T 26671492-G-T A*
16620896-C-T 14509016-C-T Z23788 Y+
15846296-G-A 13734416-G-A Y51214 YY+
4506226-T-C 4638185-T-C FT387746 +
10939629-C-T FT437409 +
6882720-A-G 7014679-A-G FT388124 YY+
2954031-G-A 3085990-G-A FT387442 +
3110193-T-C 3242152-T-C FT387469 +
3448586-G-C 3580545-G-C FT387526 +
5571732-C-G 5703691-C-G FT387953 +
7667720-C-T 7799679-C-T FT388263 YY+
8234385-C-T 8366344-C-T FT388353 YY+
8407972-G-A 8539931-G-A FT67318 YY+
8429462-G-A 8561421-G-A FT388383 YY+
9109328-A-G 9271719-A-G BY78175 Y+
10033211-G-T 10195602-G-T FT426847 Y+
10921352-A-C FT436625 +
11667424-G-A FT450993 +
13883714-G-A 11763008-G-A FT388613 Y+
14046058-C-T 11925352-C-T FT388655 YY+
14266228-A-G 12145522-A-G FT388696 YY+
14568634-C-G 12456834-C-G FT388767 Y+
14681173-A-G 12569239-A-G FT388783 Y+
15747242-T-C 13635362-T-C FT388953 YY+
15966038-T-A 13854158-T-A FT388992 YY+
16382022-G-A 14270142-G-A FT389052 Y+
16415050-G-A 14303170-G-A YY+
16836750-G-A 14724870-G-A FT389143 YY+
16855196-G-T 14743316-G-T FT389149 YY+
17031930-G-C 14920050-G-C FT389177 YY+
17981198-C-T 15869318-C-T FT389349 Y+
18109824-A-G 15997944-A-G FT389368 YY+
18620930-C-G 16509050-C-G FT389422 YY+
18956700-A-G 16844820-A-G FT389477 YY+
19481797-G-A 17369917-G-A FT389594 YY+
20735055-A-C 18573169-A-C FT452811 P4_Prx +
20835524-G-T 18673638-G-T FT390642 P4_Gap +
21289164-C-A 19127278-C-A FT389649 YY+
21396277-AT-A 19234391-AT-A +
21646248-T-C 19484362-T-C BY18396 YY+
21804867-T-C 19642981-T-C FT389756 Y+
22467020-C-T 20305134-C-T FT458746 DYZ19 +
22713090-T-C 20551204-T-C FT389856 YY+
22840025-G-A 20678139-G-A FT389874 Y+
23165971-C-A 21004085-C-A FT389920 Y+
24448064-TA-T 22301917-TA-T +
28654105-G-T 26507958-G-T FT390082 +
28725325-G-C 26579178-G-C FT390097 +
5502827-C-CTGTG 5634786-C-CTGTG 17×TG*
18890699-A-AAAGCAAGC 16778819-A-AAAGCAAGC 7×AAGC*
22294667-G-T 20132781-G-T BY31742 DYZ19 *
22319565-G-C 20157679-G-C DYZ19 *
19377431-G-A 17265551-G-A **
7001439-A-G 7133398-A-G **
3152336-G-A 3284295-G-A **
3345679-T-C 3477638-T-C **
8066406-A-G 8198365-A-G **
8813219-A-G 8945178-A-G **
8983190-G-A 9145581-G-A **
9030110-T-C 9192501-T-C **
17858846-C-A 15746966-C-A **
18913426-C-T 16801546-C-T **
19923345-C-A 17811465-C-A P5_Prx **
22423637-A-T 20261751-A-T DYZ19 **
21755129-AT-A **
24388323-T-A 22242176-T-A **
8160178-CAAAAAA-C 8292137-CAAAAAA-C 20×A***
16336897-GTTTTTT-G 14225017-GTTTTTT-G 23×T***
7984040-TAAA-T,TAA 8115999-TAAA-T,TAA 21×A***
17597154-CTTTTTT-C,CTTTTT 15485274-CTTTTTT-C,CTTTTT 20×T***
17641982-TG-T 15530102-TG-T ***
10066291-T-C 10228682-T-C ***
3618709-A-G 3750668-A-G ***
4000825-A-G 4132784-A-G ***
6093470-T-TGG 6225429-T-TGG 12×G***
9924413-GT-G 10086804-GT-G ***
10624524-G-C ***
13708881-A-T 11553205-A-T ***
14184422-CAAAAAAAA-C,CAAAAAAA 12063716-CAAAAAAAA-C,CAAAAAAA 26×A***
17260657-T-C 15148777-T-C ***
22257780-G-T 20095894-G-T DYZ19 ***
22433667-T-A 20271781-T-A DYZ19 ***
22433832-C-T 20271946-C-T DYZ19 ***
22478097-A-G 20316211-A-G DYZ19 ***
22698929-CTT-C,CTTTT 20537043-CTT-C,CTTTT 13×T***
28793901-A-G 26647754-A-G ***
56828936-TTCCATTCCATTCCA-T,TGCTATTAGATTCCA ***

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.