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 > Z5908 > Z19318 > Z5910 > 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
HG01979
18378959-C-CTT 16267079-C-CTT P6_Prx 28×T+
8675792-G-A 8807751-G-A BY839 YY+
17372073-G-A 15260193-G-A FGC34588 YY+
21892364-A-G 19730478-A-G FT348512 YY+
2680954-G-A 2812913-G-A FT344927 YY+
2721446-A-G 2853405-A-G Z35923 YY+
2834556-T-C 2966515-T-C Z35924 YY+
2852785-G-A 2984744-G-A Z35925 YY+
2882981-C-T 3014940-C-T Z35926 YY+
2898086-G-T 3030045-G-T Y+
3006965-C-A 3138924-C-A +
3008947-T-G 3140906-T-G +
3040508-C-T 3172467-C-T +
3051461-G-A 3183420-G-A +
3321825-C-T 3453784-C-T +
3734156-T-C 3866115-T-C +
3961733-C-A 4093692-C-A FT377113 +
4468496-G-A 4600455-G-A +
4842872-C-G 4974831-C-G +
4944563-T-C 5076522-T-C +
5111024-C-G 5242983-C-G +
5333356-C-T 5465315-C-T +
5365537-T-G 5497496-T-G +
5451839-A-G 5583798-A-G +
5615440-G-A 5747399-G-A +
5665551-C-T 5797510-C-T +
5789234-T-C 5921193-T-C +
6022767-G-C 6154726-G-C +
6065765-C-T 6197724-C-T +
6415709-C-T 6547668-C-T +
6713952-A-G 6845911-A-G FT345028 Y+
6772455-C-T 6904414-C-T FT345049 Y+
6953907-T-C 7085866-T-C Z35927 YY+
6975506-T-C 7107465-T-C FT345113 YY+
7012071-T-C 7144030-T-C FT345125 YY+
7217265-C-T 7349224-C-T FT345212 YY+
7265921-C-T 7397880-C-T FT345230 YY+
7270943-A-T 7402902-A-T FT345234 YY+
7547777-C-T 7679736-C-T BY65812 YY+
7548182-A-G 7680141-A-G FT345331 YY+
7622624-C-G 7754583-C-G FT345372 YY+
7624062-C-T 7756021-C-T YY+
7629787-G-A 7761746-G-A F16053 YY+
7698498-T-C 7830457-T-C Z35921 YY+
7725444-C-G 7857403-C-G FT345421 YY+
7729168-A-G 7861127-A-G FT345426 YY+
8154736-C-T 8286695-C-T FT345561 YY+
8391916-A-C 8523875-A-C FT345652 YY+
8436858-C-T 8568817-C-T BY72742 YY+
8547966-C-T 8679925-C-T BY20618 YY+
8555382-G-A 8687341-G-A FT334546 YY+
8604508-C-A 8736467-C-A FT345736 YY+
8673767-G-A 8805726-G-A FT345764 Y+
8747738-G-A 8879697-G-A FT342735 YY+
8804430-G-A 8936389-G-A FT345813 YY+
8986802-G-T 9149193-G-T +
9521935-T-C 9684326-T-C +
9999113-G-C 10161504-G-C Y+
13577862-C-A 11422186-C-A +
13840750-C-A 11720044-C-A +
13846623-C-A 11725917-C-A +
14048252-C-T 11927546-C-T FT168386 YY+
14171303-A-G 12050597-A-G FT346198 YY+
14171320-A-G 12050614-A-G FT346199 YY+
14172311-T-C 12051605-T-C FT346200 YY+
14480058-C-T 12359327-C-T FT346342 YY+
14783730-C-T 12671800-C-T FT346430 YY+
14947134-C-T 12835208-C-T FT160279 YY+
15270137-C-T 13158226-C-T FT346572 YY+
15729468-G-T 13617588-G-T FT346715 YY+
15756971-G-A 13645091-G-A Z41284 YY+
15758525-A-G 13646645-A-G FT346733 YY+
15922795-G-A 13810915-G-A FT346794 Y+
16002318-C-T 13890438-C-T F20365 Y+
16024217-G-A 13912337-G-A Y+
16025908-C-T 13914028-C-T Y+
16198647-G-A 14086767-G-A FT346879 YY+
16354097-A-G 14242217-A-G FT346946 Y+
16651823-C-G 14539943-C-G FT347066 YY+
16899949-G-A 14788069-G-A FT347162 YY+
16907526-T-C 14795646-T-C FT347168 YY+
17059560-T-C 14947680-T-C Y+
17079882-G-A 14968002-G-A FT187583 YY+
17170392-G-T 15058512-G-T FT347268 YY+
17468751-C-T 15356871-C-T FT347388 YY+
17902863-C-A 15790983-C-A FT347549 Y+
18119207-T-C 16007327-T-C FT347651 YY+
18397921-AAT-A 16286041-AAT-A P6_Gap +
18540423-G-C 16428543-G-C Y+
18710178-G-A 16598298-G-A YY+
18745076-A-G 16633196-A-G FT347804 YY+
19053798-T-G 16941918-T-G FT347921 YY+
19136459-A-T 17024579-A-T FT347960 YY+
19144921-C-T 17033041-C-T FT347964 YY+
19149681-A-G 17037801-A-G FT347966 YY+
19285907-G-A 17174027-G-A FT348017 YY+
19321787-T-C 17209907-T-C FT348033 YY+
19561636-T-G 17449756-T-G Y+
19561709-A-G 17449829-A-G Y+
20947963-C-T 18786077-C-T P4_Dst +
21155194-A-G 18993308-A-G Y+
21216843-A-T 19054957-A-T FT348243 YY+
21262353-C-A 19100467-C-A FT348263 YY+
21581068-A-G 19419182-A-G Y+
21588893-A-G 19427007-A-G FT348400 Y+
21842539-C-A 19680653-C-A FT348492 Y+
21862594-G-A 19700708-G-A FT348498 YY+
22058118-T-A 19896232-T-A FT348573 Y+
22459411-A-T 20297525-A-T DYZ19 +
22466827-G-T 20304941-G-T BY45526 DYZ19 +
22467253-G-A 20305367-G-A FT406566 DYZ19 +
22509688-A-G 20347802-A-G DYZ19 +
22644623-T-C 20482737-T-C FT348689 Y+
22673929-A-T 20512043-A-T FT348696 YY+
22967155-T-C 20805269-T-C FT348799 YY+
23043433-C-T 20881547-C-T M7084 YY+
23186334-C-G 21024448-C-G FT348890 Y+
23521660-T-G 21359774-T-G FT349017 Y+
23537510-A-C 21375624-A-C FT349021 YY+
23641780-G-A 21479894-G-A Y+
23730589-C-G 21568703-C-G +
23984437-T-C 21838290-T-C FT349109 Y+
28544777-G-A 26398630-G-A FT349210 +
28586295-G-T 26440148-G-T FT349231 +
28679027-T-C 26532880-T-C FT349276 +
28773518-C-G 26627371-C-G Z35922 +

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.