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] > M2335 > F346[NO] > P191[O] > 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
HG02047
22164428-G-T 20002542-G-T FT302599 YY+
2769407-G-A 2901366-G-A FT344955 Y+
2900337-G-T 3032296-G-T FT280321 Y+
3391909-A-G 3523868-A-G +
4141672-T-C 4273631-T-C +
4219581-C-G 4351540-C-G +
4291218-T-C 4423177-T-C +
4592566-C-A 4724525-C-A +
4673118-A-G 4805077-A-G +
4737599-T-C 4869558-T-C +
4979394-C-G 5111353-C-G FGC54470 +
5854641-T-C 5986600-T-C +
6904939-A-G 7036898-A-G F15439 YY+
7177575-T-C 7309534-T-C FT345192 YY+
7189320-G-T 7321279-G-T F921 YY+
7388527-G-C 7520486-G-C F15858 YY+
7594967-G-A 7726926-G-A FT345354 YY+
7705190-C-T 7837149-C-T Y16155 Y+
7905628-G-A 8037587-G-A F16407 YY+
8008773-G-T 8140732-G-T FT345505 YY+
8143574-A-G 8275533-A-G Y15975 YY+
8205381-C-T 8337340-C-T Y15976 YY+
8520767-C-G 8652726-C-G F17176 YY+
8847467-T-C 8979426-T-C F17539 YY+
9079394-A-G 9241785-A-G FT345915 +
9412554-A-C 9574945-A-C Y26385 Y+
9988395-C-T 10150786-C-T Y+
10054184-A-G 10216575-A-G +
13359943-G-A 11204267-G-A +
13716901-C-T 11561225-C-T Z2108Z2108 +
13805242-G-A 11684536-G-A BY90078 +
14033846-G-T 11913140-G-T F1676 YY+
14107063-G-T 11986357-G-T FGC54467 YY+
14327675-T-A 12206969-T-A F18809 YY+
14345136-T-C 12224431-T-C F18834 YY+
15014836-A-G 12902924-A-G FT346509 YY+
15141790-A-G 13029877-A-G FT346547 Y+
15785608-C-T 13673728-C-T F20155 YY+
15943040-G-A 13831160-G-A Y15977 YY+
16253567-A-G 14141687-A-G F2109 YY+
16374286-G-C 14262406-G-C FT346954 YY+
16478855-T-G 14366975-T-G F20733 YY+
16535289-A-G 14423409-A-G F20792 YY+
16569722-A-G 14457842-A-G F20842 YY+
16657691-T-A 14545811-T-A Y+
17369384-T-C 15257504-T-C F21683 YY+
17395298-G-A 15283418-G-A F21709 YY+
17734133-A-C 15622253-A-C FGC54466 Y+
18059652-C-A 15947772-C-A FT347622 YY+
18077946-G-T 15966066-G-T F22417 YY+
18137992-C-T 16026112-C-T BY65800Y15978 YY+
19196804-G-A 17084924-G-A F23419 YY+
19416445-C-T 17304565-C-T Y+
19463244-A-G 17351364-A-G FT348085 Y+
19545395-C-T 17433515-C-T FT348111 YY+
21057112-G-A 18895226-G-A Y+
21128804-C-G 18966918-C-G FT348224 YY+
21316063-A-C 19154177-A-C F24147 YY+
21340805-T-G 19178919-T-G F24181 YY+
21505558-A-G 19343672-A-G YY+
21572665-T-C 19410779-T-C FT348395 YY+
21981434-G-A 19819548-G-A F24884 YY+
22062174-A-C 19900288-A-C FT348575 YY+
22083427-A-G 19921541-A-G FT348584 YY+
22241940-C-A 20080054-C-A DYZ19 +
22420104-G-T 20258218-G-T FT455945 DYZ19 +
22458097-G-C 20296211-G-C DYZ19 +
22461938-G-C 20300052-G-C FT213914 DYZ19 +
23047506-A-C 20885620-A-C Y15979 YY+
23133271-T-A 20971385-T-A Y15980 YY+
23205081-A-C 21043195-A-C Y+
23205373-C-T 21043487-C-T FT348905 Y+
23525466-A-G 21363580-A-G F3452 YY+
23815848-T-C 21653962-T-C F26411 Y+
24421226-T-A 22275079-T-A Y15981 Y+
28473040-G-A 26326893-G-A +

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.