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 > CTS2731 > 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
NA19729
13686912-C-G 11531236-C-G 10×GAATG+
23198870-G-A 21036984-G-A CTS11628 Y+
3186017-A-G 3317976-A-G +
13362233-C-A 11206557-C-A +
2785897-A-G 2917856-A-G CTS177 YY+
3170437-G-A 3302396-G-A FT152021 +
3436432-G-A 3568391-G-A L451 +
3453169-A-G 3585128-A-G FT152112 +
3924639-T-C 4056598-T-C +
3987186-T-C 4119145-T-C FT152283 +
4416742-C-G 4548701-C-G FT152400 +
4418420-A-T 4550379-A-T +
4527196-A-G 4659155-A-G +
4529860-C-T 4661819-C-T +
4850385-C-T 4982344-C-T FT152521 +
5216697-A-T 5348656-A-T +
5330955-G-A 5462914-G-A FT152673 +
5383165-C-T 5515124-C-T FT152695 +
5452751-G-C 5584710-G-C FT152715 +
5454074-C-A 5586033-C-A FT152716 +
5783141-C-T 5915100-C-T FT152817 +
6007321-G-A 6139280-G-A +
6435317-C-G 6567276-C-G +
6535489-T-C 6667448-T-C FT152980 +
7029363-C-T 7161322-C-T CTS811 Y+
7159282-C-A 7291241-C-A YY+
7169884-C-A 7301843-C-A CTS1046 YY+
7207292-C-A 7339251-C-A YY+
7509566-T-G 7641525-T-G BZ4052 Y+
7614436-C-T 7746395-C-T BY7442 YY+
7625850-A-G 7757809-A-G BZ4053 YY+
7748584-T-A 7880543-T-A BZ4054 YY+
7752297-A-T 7884256-A-T BZ4055 YY+
7929888-C-T 8061847-C-T YY+
7950484-G-T 8082443-G-T YY+
7977540-C-T 8109499-C-T FT179174 YY+
8072522-C-T 8204481-C-T FT153286 YY+
8523605-A-G 8655564-A-G BZ4057 YY+
8544313-A-T 8676272-A-T YY+
8711847-T-C 8843806-T-C YY+
9099405-A-G 9261796-A-G FT295684 Y+
9138844-T-C 9301235-T-C BZ4060 Y+
9481157-G-T 9643548-G-T BZ4061 +
9733454-A-C 9895845-A-C IR3_Prx +
9822872-A-C 9985263-A-C BZ4062 YY+
9939435-C-T 10101826-C-T Y+
13127440-A-T 10616926-A-T +
13424289-T-C 11268613-T-C +
13457760-C-G 11302084-C-G +
13810501-A-T 11689795-A-T +
13817377-G-A 11696671-G-A FT121647 +
13892152-T-C 11771446-T-C Y+
14008045-G-A 11887339-G-A CTS1657 YY+
14212851-G-T 12092145-G-T Y+
14317937-A-T 12197231-A-T YY+
14423023-G-C 12302298-G-C CTS2677 YY+
14504405-T-C 12392610-T-C YY+
14504427-T-A 12392632-T-A CTS2822 YY+
14530900-GTA-G 12419101-GTA-G +
14545288-C-A 12433489-C-A CTS2894 YY+
14555147-G-A 12443348-G-A YY+
14921572-C-T 12809637-C-T CTS3435 YY+
15098438-G-T 12986526-G-T CTS3665 Y+
15142881-T-A 13030968-T-A Y+
15249677-A-G 13137763-A-G CTS3899 Y+
15394089-A-G 13282209-A-G YY+
15403501-G-A 13291621-G-A CTS4114 YY+
15466217-G-A 13354337-G-A CTS4194 YY+
15692499-A-G 13580619-A-G CTS4522 YY+
15996301-A-T 13884421-A-T CTS5061 YY+
16208808-C-T 14096928-C-T CTS5324 Y+
16361045-C-A 14249165-C-A CTS5557 YY+
16654796-T-G 14542916-T-G CTS6079 YY+
16737166-G-T 14625286-G-T YY+
16746375-G-A 14634495-G-A BZ4067 YY+
16865336-A-T 14753456-A-T CTS6382 YY+
17104661-G-A 14992781-G-A YY+
17174615-C-A 15062735-C-A YY+
17446298-G-A 15334418-G-A CTS7371 YY+
17535149-T-C 15423269-T-C Y+
17907784-C-A 15795904-C-A CTS8270 YY+
18041507-C-G 15929627-C-G CTS8466 Y+
18163488-A-G 16051608-A-G CTS8721 YY+
18202067-T-A 16090187-T-A CTS8789 YY+
18217740-A-T 16105860-A-T Y+
18239803-C-T 16127923-C-T BZ4068 Y+
18648717-G-A 16536837-G-A BZ4069 YY+
18782169-C-T 16670289-C-T CTS9257 YY+
19229131-G-T 17117251-G-T YY+
19364376-T-G 17252496-T-G CTS10274 YY+
19438612-G-A 17326732-G-A FT154828 YY+
19478303-A-G 17366423-A-G CTS10483 YY+
21185896-T-C 19024010-T-C BZ4074 YY+
21219620-G-T 19057734-G-T YY+
21287725-A-C 19125839-A-C BZ4076 YY+
21365229-C-G 19203343-C-G BZ4077 YY+
21417161-C-T 19255275-C-T FT298433 Y+
21484674-G-A 19322788-G-A BZ4078 YY+
21611347-A-C 19449461-A-C BZ4079 YY+
21700690-A-G 19538804-A-G YY+
21734788-A-G 19572902-A-G BZ4081 YY+
21773255-C-T 19611369-C-T BZ4082 YY+
21774501-A-G 19612615-A-G BZ4083 YY+
21781415-C-A 19619529-C-A YY+
22113643-C-G 19951757-C-G FT298856 YY+
22204821-G-A 20042935-G-A BY138450 Y+
22217345-A-G 20055459-A-G DYZ19 +
22218064-A-T 20056178-A-T DYZ19 +
22254883-T-C 20092997-T-C DYZ19 +
22255721-G-C 20093835-G-C DYZ19 +
22458127-G-C 20296241-G-C FT457251 DYZ19 +
22460288-T-G 20298402-T-G DYZ19 +
22466750-C-G 20304864-C-G BY221771 DYZ19 +
22484589-A-G 20322703-A-G DYZ19 +
22485061-T-C 20323175-T-C DYZ19 +
22679351-C-A 20517465-C-A YY+
22898397-G-A 20736511-G-A CTS11014 YY+
23032883-G-C 20870997-G-C CTS11246 YY+
23327533-G-A 21165647-G-A CTS11872 YY+
23338453-G-T 21176567-G-T CTS11899 Y+
23458089-A-G 21296203-A-G BZ4085 YY+
23521573-A-T 21359687-A-T FT299381 Y+
23552609-G-T 21390723-G-T YY+
23740298-G-A 21578412-G-A BZ4087 +
23954899-T-C 21808752-T-C BY148723 +
24461604-C-T 22315457-C-T BZ4088 Y+
28529861-T-C 26383714-T-C CTS12221 Y+
28572581-G-T 26426434-G-T CTS12310 +
28617272-C-A 26471125-C-A CTS12571 +
28696271-T-A 26550124-T-A +
28722571-A-T 26576424-A-T FT155516 +
28750913-G-A 26604766-G-A CTS12917 +
28790246-G-A 26644099-G-A BZ4090 +

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.