Tree Position

R-P312/S116 > Z40481 > ZZ11 > DF27/S250 > ZZ12 > Z46512 > FGC20747 > FGC20764 > FGC20767 > FGC20770 > BY27772 > Y17780

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 STRFTDNA
B43396
BigY3
B43396
18459753-G-GA 16347873-G-GA P6_Dst A+
4327804-G-A 4459763-G-A A*
6223236-G-A 6355195-G-A IR3_Dst ***A*
19742161-A-G 17630281-A-G P5_Prx ***A*
22274318-G-T 20112432-G-T DYZ19 ***A*
22308649-G-C 20146763-G-C DYZ19 ***A*
26079812-G-A 23933665-G-A P1_Y1 ***A*
3884178-G-A 4016137-G-A A*
4328067-T-C 4460026-T-C A*
4556175-C-A 4688134-C-A A*
4556903-T-C 4688862-T-C A*
13449594-T-C 11293918-T-C A*
18349341-A-AT 16237461-A-AT P6_Prx A*
19708280-G-A 17596400-G-A P5_Prx A*
22256940-C-A 20095054-C-A DYZ19 A*
26077558-C-T 23931411-C-T P1_Y1 A*
28817468-A-C 26671321-A-C A*
22920121-G-A 20758235-G-A PH93PH5265 YY++
7246823-A-T 7378782-A-T F15717 YY++
5851773-C-A 5983732-C-A BY58888 **+
6765017-G-A 6896976-G-A Y82483 YY++
8025671-A-G 8157630-A-G Y85638 YY++
8301689-C-A 8433648-C-A BY71517 YY++
8369326-C-T 8501285-C-T Y86631 YY++
14843650-A-G 12731716-A-G Y92334 YY++
14863858-A-G 12751924-A-G Y92378 YY++
16957629-GAC-G 14845749-GAC-G ++
17357991-C-T 15246111-C-T Y98911 YY++
17437784-A-G 15325904-A-G Y99146 YY++
17524383-T-C 15412503-T-C Y99418 YY++
17673279-G-C 15561399-G-C Y99891 YY++
17705474-A-C 15593594-A-C Y99985 YY++
17780267-A-T 15668387-A-T Y100198 YY++
18668774-T-C 16556894-T-C Y102377 YY++
18705705-C-T 16593825-C-T Y102471 YY++
20105762-CT-C 17993882-CT-C P5_Dst +
20137798-G-A 18025918-G-A P5_Dst +**
21160398-T-A 18998512-T-A Y105582 YY++
21917384-T-C 19755498-T-C Y107876 YY++
21951177-A-G 19789291-A-G Y107976 YY++
21961002-AATAG-A 19799116-AATAG-A +**
22179612-T-TA 20017726-T-TA +***
22479098-G-A 20317212-G-A BY224159 DYZ19 +**
22712385-G-C 20550499-G-C Y109537 YY++
23796345-G-A 21634459-G-A Y112330 Y++
23062720-C-T 20900834-C-T FT97239 YY+
11646627-G-T FT165092 +
14373736-C-T 12253032-C-T FT160183 YY+
4191937-C-T 4323896-C-T FT158843 +
4308682-T-A 4440641-T-A FT73213 +
4309787-G-A 4441746-G-A FT158861 +
4351047-C-T 4483006-C-T FT158875 +
4670893-G-A 4802852-G-A FT158965 +
4837492-C-T 4969451-C-T FT39282 +
5051255-C-T 5183214-C-T FT159070 +
5898928-G-A 6030887-G-A FT159286 +
6478200-C-T 6610159-C-T FT159378 +
10800289-C-T FT431770 +
13873571-G-T 11752865-G-T FT160026 Y+
13930102-G-A 11809396-G-A FT160047 Y+
15370377-T-C 13258497-T-C FT160356 Y+
21962296-G-A 19800410-G-A YY+
22057828-G-A 19895942-G-A FT161470 Y+
22057830-G-A 19895944-G-A FT161471 Y+
28507256-T-C 26361109-T-C Y+
28565555-C-T 26419408-C-T FT161878 +
3899405-G-C 4031364-G-C *
3927346-C-T 4059305-C-T *
4208305-A-G 4340264-A-G *
5680232-C-G 5812191-C-G *
4208304-C-T 4340263-C-T *
4444188-T-C 4576147-T-C *
4577565-G-C 4709524-G-C *
22233701-A-G 20071815-A-G DYZ19 ****
22977539-A-AATACATAC 20815653-A-AATACATAC 11×ATAC*
20023980-A-AGAT 17912100-A-AGAT P5_Prx ****
22254025-T-A 20092139-T-A DYZ19 ****
22319606-C-A 20157720-C-A DYZ19 ****
3423987-A-C 3555946-A-C *
3425561-AT-A 3557520-AT-A *
3430175-C-T 3562134-C-T *
3496642-C-T 3628601-C-T *
4035820-C-T 4167779-C-T *
10662762-C-G *
22298282-G-A 20136396-G-A BY52416 DYZ19 *****
24096070-T-C 21949923-T-C BY225982 P3_b1 *****
3443764-TTTATTATTATTA-T 3575723-TTTATTATTATTA-T 12×TTA**
3496670-G-A 3628629-G-A **
10624573-A-AT **
13360605-G-A 11204929-G-A **
13573548-G-T 11417872-G-T FT350539 **
14161654-A-AT 12040948-A-AT **
19709992-C-A 17598112-C-A P5_Prx **
22476898-T-A 20315012-T-A DYZ19 **
22429573-G-A 20267687-G-A DYZ19 ***
9985151-G-A 10147542-G-A ***
15799114-C-CCCTT 13687234-C-CCCTT 14×CCTT***
22438370-C-A 20276484-C-A BY218536 DYZ19 ***
9364095-C-T 9526486-C-T ***
22230367-T-A 20068481-T-A DYZ19 ******
22250667-T-A 20088781-T-A DYZ19 ***
22251067-C-A 20089181-C-A DYZ19 ***
22274989-T-C 20113103-T-C DYZ19 ******
22335221-G-C 20173335-G-C DYZ19 ***
22346444-G-T 20184558-G-T DYZ19 ***
22365158-G-A 20203272-G-A DYZ19 ***
22368283-G-A 20206397-G-A DYZ19 ***
22435964-A-G 20274078-A-G DYZ19 ***
22441828-A-G 20279942-A-G DYZ19 ***
22454150-T-A 20292264-T-A DYZ19 ***
22485293-C-A 20323407-C-A DYZ19 ***
22510960-A-T 20349074-A-T DYZ19 ***
24106728-G-C 21960581-G-C P3_b1 ***
24818286-A-C 22672139-A-C P3_b2 ***
25181318-T-C 23035171-T-C g1 ***
11009021-C-A ***
17086886-G-A 14975006-G-A ***
28818615-A-C 26672468-A-C ***
3107813-C-T 3239772-C-T ***
3792282-A-G 3924241-A-G ***
3899386-T-C 4031345-T-C ***
6024966-A-G 6156925-A-G ***
7164467-CAAAAAAA-C,CAAAA 7296426-CAAAAAAA-C,CAAAA 24×A***
13606877-CAAA-C,CA 11451201-CAAA-C,CA 25×A***
15011290-A-G 12899375-A-G ***
17625903-A-G 15514023-A-G ***
21055047-T-C 18893161-T-C ***

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.