Tree Position

A0-T-YP2191 > P305[A1] > A1b > A1b1

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
NA21313
18892211-A-T 16780331-A-T PF945 YY+
9919267-G-A 10081658-G-A Y+
10063995-G-A 10226386-G-A FGC61956 +
9935299-C-A 10097690-C-A Y+
19646396-TG-T 17534516-TG-T P5_Prx +
13616426-G-C 11460750-G-C +
2735743-G-T 2867702-G-T YY+
2915225-G-A 3047184-G-A FT129528 Y+
3049055-G-A 3181014-G-A FT6848 +
3109932-C-A 3241891-C-A FT6875 +
3156154-C-G 3288113-C-G FT6897 +
3238461-C-T 3370420-C-T FTA34451 +
3846777-G-C 3978736-G-C FT7208 +
3938012-T-A 4069971-T-A +
4071389-C-T 4203348-C-T +
4071974-T-A 4203933-T-A +
4380550-T-C 4512509-T-C FT7444 +
4585084-A-T 4717043-A-T FT7534 +
4712268-C-A 4844227-C-A FT7583 +
4838292-C-T 4970251-C-T FT7623 +
4940390-A-C 5072349-A-C FGC38069 +
4991506-T-C 5123465-T-C FT159054 +
5003718-C-T 5135677-C-T FT7686 +
5829520-A-G 5961479-A-G FT8080 +
5937828-C-G 6069787-C-G +
6058052-T-C 6190011-T-C +
6772197-T-C 6904156-T-C FTB15712 Y+
6903058-G-A 7035017-G-A Y+
7037505-A-G 7169464-A-G YY+
7101167-C-T 7233126-C-T Y+
7161602-C-T 7293561-C-T YY+
7161795-G-A 7293754-G-A FGC40000 YY+
7373985-G-A 7505944-G-A Y+
7597228-C-A 7729187-C-A V1247 YY+
7664160-T-C 7796119-T-C Y26828 YY+
7698359-T-C 7830318-T-C V1377 YY+
7779927-T-C 7911886-T-C V1429 YY+
7850953-C-G 7982912-C-G FGC40014 YY+
7999238-A-G 8131197-A-G SK251 V1559 YY+
8055097-G-A 8187056-G-A FGC39990 YY+
8444853-G-A 8576812-G-A FGC39998 YY+
8677789-A-T 8809748-A-T FGC40009 YY+
8860260-C-T 8992219-C-T FGC39995 YY+
10000515-T-A 10162906-T-A Y+
10063884-T-G 10226275-T-G +
10077981-T-C 10240372-T-C +
13397938-T-C 11242262-T-C +
13402152-A-AT 11246476-A-AT +
13405154-TA-T 11249478-TA-T +
13406309-T-C 11250633-T-C +
13409550-C-T 11253874-C-T +
13455400-A-G 11299724-A-G +
13489885-C-G 11334209-C-G BY210394 +
13503599-GTA-G 11347923-GTA-G +
13637863-A-G 11482187-A-G FT92489 +
14177939-C-G 12057233-C-G Y26830 YY+
14178311-T-C 12057605-T-C Y25079 Y+
14186836-A-T 12066130-A-T Y26831 YY+
14213506-G-A 12092800-G-A FGC40001 YY+
14230827-G-T 12110121-G-T YY+
14234027-C-G 12113321-C-G YY+
14306289-A-C 12185583-A-C Y25080 Y+
14372942-T-C 12252238-T-C M9740 YY+
14399874-C-T 12279171-C-T FGC40006 YY+
14594999-A-T 12483199-A-T M9756 YY+
15086569-A-C 12974659-A-C SK241 V2816 YY+
15345471-G-C 13233590-G-C YY+
15377871-T-C 13265991-T-C FT336109 Y+
15575750-G-A 13463870-G-A V3042 YY+
15637701-G-A 13525821-G-A Y+
15746142-C-T 13634262-C-T Y26832 Y+
15776680-G-A 13664800-G-A YY+
15778697-G-A 13666817-G-A FGC40007 YY+
15922509-G-A 13810629-G-A FT336469 Y+
16063661-G-T 13951781-G-T Y26833 Y+
16197265-G-A 14085385-G-A YY+
16257481-G-A 14145601-G-A YY+
16350257-G-A 14238377-G-A YY+
16433397-G-A 14321517-G-A FGC39994 YY+
16625554-T-C 14513674-T-C Y25081 Y+
16628250-A-G 14516370-A-G YY+
16691460-C-T 14579580-C-T Y26834 YY+
16700571-G-C 14588691-G-C M9940 Y+
16868426-G-A 14756546-G-A Y97545 BY34446 YY+
16870474-T-A 14758594-T-A FGC40003 YY+
16975293-G-A 14863413-G-A Y+
17315947-G-A 15204067-G-A FGC39996 YY+
17540017-A-G 15428137-A-G Y25083 Y+
17889777-G-A 15777897-G-A Y26838 YY+
17897572-T-C 15785692-T-C Y26839 YY+
17933488-C-G 15821608-C-G Y26840 Y+
18381781-T-A 16269901-T-A SK252 P6_Gap +
18552247-A-G 16440367-A-G SK244 Y+
18725492-T-C 16613612-T-C V3447 FGC39993 YY+
18746161-G-C 16634281-G-C FGC39997 YY+
18768036-A-T 16656156-A-T FGC40004 Y+
18844394-C-T 16732514-C-T Y26841 Y+
18865630-C-G 16753750-C-G V3561 YY+
18917858-A-G 16805978-A-G V3602 YY+
18971871-A-G 16859991-A-G Y26842 YY+
19017995-C-A 16906115-C-A Y25084 Y+
21203352-C-T 19041466-C-T BY18845 Y25085 YY+
21573040-T-A 19411154-T-A YY+
21655571-A-C 19493685-A-C BY36196 Y76912 YY+
21677240-G-A 19515354-G-A FT218012 Y+
21689144-C-G 19527258-C-G A8423 YY+
21844654-G-C 19682768-G-C SK239 YY+
21963789-A-T 19801903-A-T YY+
22152786-C-T 19990900-C-T Y+
22173976-G-A 20012090-G-A YY+
22217655-C-A 20055769-C-A DYZ19 +
22220390-G-A 20058504-G-A PF1105 DYZ19 +
22244805-A-T 20082919-A-T DYZ19 +
22246042-G-A 20084156-G-A DYZ19 +
22281433-G-C 20119547-G-C BY31511 DYZ19 +
22293888-C-A 20132002-C-A PF1142 DYZ19 +
22301407-G-T 20139521-G-T DYZ19 +
22685238-T-G 20523352-T-G FGC40010 YY+
22785613-G-T 20623727-G-T FGC40013 YY+
22799296-C-A 20637410-C-A Y25086 Y+
22953011-C-G 20791125-C-G YY+
23099098-C-T 20937212-C-T FGC39992 YY+
23226865-G-A 21064979-G-A Y+
23397304-C-T 21235418-C-T YY+
24367028-G-A 22220881-G-A FGC39999 +
27391309-A-G 25245162-A-G FGC38172 P1_g3 +
28564223-G-A 26418076-G-A Y26844 +
28620513-A-G 26474366-A-G Y+
28809225-T-A 26663078-T-A +
58968236-C-CTA 56822089-C-CTA +

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.