Tree Position

R-P312/S116 > Z40481 > ZZ11 > DF27/S250 > Z195/S355 > Z198 > Z46513 > FGC35855

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
21596
15226035-C-T 13114121-C-T YA+
20623169-C-T 18461283-C-T P4_Prx A*
13687233-C-T 11531557-C-T A*
56833678-C-A A*
4546684-C-T 4678643-C-T A*
7270936-T-TA 7402895-T-TA 10×AA*
14435541-C-T 12314814-C-T YA*
17143169-T-TA 15031289-T-TA 10×AA*
19709695-G-C 17597815-G-C P5_Prx A*
19791737-T-C 17679857-T-C P5_Prx A*
20004347-C-G 17892467-C-G P5_Prx A*
23714665-A-G 21552779-A-G A*
26099375-C-T 23953228-C-T P1_Y1 A*
26109376-C-T 23963229-C-T P1_Y1 A*
26296784-G-A 24150637-G-A P1_Y1 A*
26297376-T-C 24151229-T-C P1_Y1 A*
26424576-G-A 24278429-G-A P1_Y1 A*
14504451-C-T 12392656-C-T BY23532Z32810 YY+
22712953-G-A 20551067-G-A BY140246 YY+
13228437-G-A 11072761-G-A BY84683 +
8660258-C-T 8792217-C-T FT8775 YY+
9046782-C-A 9209173-C-A FT407701 Y+
5265430-G-A 5397389-G-A FT407135 +
5668760-C-A 5800719-C-A +
5860193-C-T 5992152-C-T FT407250 +
6054027-C-G 6185986-C-G FT407281 +
6826572-A-G 6958531-A-G FT407360 YY+
6930914-C-G 7062873-C-G FT266043 Y+
7767544-G-T 7899503-G-T FT407509 YY+
7785687-A-G 7917646-A-G FT407511 YY+
8785334-C-G 8917293-C-G FT407671 YY+
9117019-A-C FT407692 +
9125246-C-T FT407694 +
9483062-T-C 9645453-T-C FT407744 +
9965804-C-T 10128195-C-T FT426641 Y+
10848731-T-C FT433986 +
10851735-T-A FT434125 +
13828328-A-G 11707622-A-G FT407798 +
13982227-C-A 11861521-C-A FT407832 Y+
14044368-G-T 11923662-G-T FT407853 YY+
14277841-G-C 12157135-G-C FT407898 YY+
14384290-A-G 12263586-A-G FT407920 Y+
15039946-G-A 12928036-G-A FT407999 YY+
15062304-T-C 12950396-T-C FT408005 YY+
15160828-T-C 13048914-T-C FT408015 YY+
15371574-G-T 13259694-G-T FT408046 YY+
15460702-T-G 13348822-T-G FT408066 YY+
15487522-T-C 13375642-T-C FT408069 YY+
15697792-AG-A 13585912-AG-A +
16951691-A-G 14839811-A-G FT42465 YY+
17166028-A-T 15054148-A-T FT408343 YY+
17242200-G-A 15130320-G-A 10824936-G-A YY+
17374883-G-A 15263003-G-A FT408391 Y+
17897135-A-G 15785255-A-G FT408496 YY+
18122898-CAGCCTGA-C 16011018-CAGCCTGA-C +
18388162-G-T 16276282-G-T FT408574 P6_Gap +
18551161-G-A 16439281-G-A FT408592 Y+
18911930-C-T 16800050-C-T FT408640 YY+
19402596-C-T 17290716-C-T FT408748 YY+
19498799-G-T 17386919-G-T FT408765 YY+
21717886-T-C 19556000-T-C FT408892 YY+
21795635-T-C 19633749-T-C FT408899 Y+
21982107-C-G 19820221-C-G FT408926 YY+
22256696-C-T 20094810-C-T FT453861 DYZ19 +
22513121-T-C 20351235-T-C FT408960 Y+
22513200-GT-G 20351314-GT-G +
22571543-A-G 20409657-A-G FT408972 YY+
22795224-C-T 20633338-C-T FT189204 YY+
24447973-C-T 22301826-C-T BY165635 Y+
28581287-T-C 26435140-T-C FT409249 +
20842517-G-GGAAAGAAA 18680631-G-GGAAAGAAA P4_Dst 14×GAAA*
3440982-T-G 3572941-T-G *
3407002-A-G 3538961-A-G *
13253350-G-A 11097674-G-A *
9459384-T-TTG 9621775-T-TTG 18×TG*
13675019-CATGGAATGGA-C 11519343-CATGGAATGGA-C 7×ATGGA*
22278537-G-A 20116651-G-A BY215811 DYZ19 *
22227390-G-A 20065504-G-A DYZ19 *
22281194-G-C 20119308-G-C DYZ19 *
18841282-A-G 16729402-A-G FGC22875 **
9671339-CT-C 9833730-CT-C IR3_Prx 14×T**
15801166-T-A 13689286-T-A BY20603Y22839 **
28804051-G-T 26657904-G-T **
22246982-T-A 20085096-T-A DYZ19 **
16104375-C-A 13992495-C-A P8_Prx 19×T**
23034499-C-A 20872613-C-A **
19435800-T-A 17323920-T-A **
3380354-T-A 3512313-T-A FT161984FT95018 **
2916088-G-A 3048047-G-A **
3437475-A-G 3569434-A-G **
14008828-G-A 11888122-G-A **
17654082-G-GT 15542202-G-GT **
20470078-C-G 18308192-C-G P5_Dst **
25951420-G-T 23805273-G-T P1_Y1 **
26311626-C-A 24165479-C-A P1_Y1 **
24461833-C-CAATA 22315686-C-CAATA 9×AATA***
6604084-CTTT-C 6736043-CTTT-C 17×T***
4237302-ATG-A 4369261-ATG-A 9×TG***
21402181-CTTT-C 19240295-CTTT-C 34×T***
19239099-TTCTA-T 17127219-TTCTA-T ***
56850710-C-A ***
18556556-C-CTGTG 16444676-C-CTGTG 15×TG***
22230350-C-A 20068464-C-A DYZ19 ***
56862621-CTTT-C,CTTTT 14×T***
21367690-A-AT,ATT 19205804-A-AT,ATT 14×T***
3240729-C-T 3372688-C-T ***
2678523-T-C 2810482-T-C ***
4076256-CAAA-C,CA 4208215-CAAA-C,CA 21×A***
5883843-G-A 6015802-G-A ***
13607598-CAA-C,CAAA 11451922-CAA-C,CAAA 18×A***
15676491-A-G 13564611-A-G ***
17926569-A-G 15814689-A-G ***
18035665-CTTT-C,CTT 15923785-CTTT-C,CTT 30×T***
18195154-ATTTT-A,ATT 16083274-ATTTT-A,ATT 29×T***
23440957-T-C 21279071-T-C ***
23951454-T-C 21805307-T-C ***
26437169-CAAA-C,CAAAA 24291022-CAAA-C,CAAAA P1_Y1 28×A***
28602505-AT-A,ATTT 26456358-AT-A,ATTT 19×T***

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.