Tree Position

R-P312/S116 > L238/S182 > Y82199

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
17803911-T-C 15692031-T-C Y100271 YY+
9645430-A-G 9807821-A-G Y89107 IR3_Prx +
16228374-G-A 14116494-G-A Y95663 YY+
15437232-C-T 13325352-C-T Y93795 YY+
15360826-A-G 13248946-A-G Y93630 YY+
15255413-A-T 13143499-A-T Y93357 YY+
15133158-A-T 13021245-A-T Y93103 YY+
15006637-T-C 12894722-T-C Y92763 YY+
17194902-T-C 15083022-T-C Y98436 YY+
13826026-C-T 11705320-C-T BY90703 +
17275741-GA-G 15163861-GA-G 9×A+
18413395-A-G 16301515-A-G Y101943 P6_Gap +
18415494-C-T 16303614-C-T Y101957 P6_Gap +
9868592-C-T 10030983-C-T BY81616 YY+
8664139-T-C 8796098-T-C Y87658 YY+
16578388-C-T 14466508-C-T Y96747 YY+
8612763-T-C 8744722-T-C Y87488 YY+
8439992-A-G 8571951-A-G Y86869 YY+
7694728-C-A 7826687-C-A Y84693 YY+
18415527-A-T 16303647-A-T Y101958 P6_Gap +
18908826-T-C 16796946-T-C Y103012 YY+
19136273-C-A 17024393-C-A Y103768 YY+
21135309-A-G 18973423-A-G Y105500 YY+
21687624-C-T 19525738-C-T Y107215 YY+
21835546-G-A 19673660-G-A Y107632 Y+
22465665-T-C 20303779-T-C BY27587 DYZ19 +
22558756-T-C 20396870-T-C Y109084 YY+
23347803-A-C 21185917-A-C Y111340 YY+
23849364-T-C 21687478-T-C BY148347 Y+
16494396-TAGAGAGAGAG-T 14382516-TAGAGAGAGAG-T 10×AG+
19472571-C-A 17360691-C-A **
3696066-G-T 3828025-G-T **
13690681-A-G 11535005-A-G BY88629 **
22349598-T-G 20187712-T-G DYZ19 **
13828451-A-C 11707745-A-C ***
24071894-T-C 21925747-T-C P3_b1 ***
22452576-T-G 20290690-T-G DYZ19 ***
9960046-G-A 10122437-G-A PF2907 ***
13650558-G-A 11494882-G-A ***
22464180-C-G 20302294-C-G DYZ19 ***
24962455-C-A 22816308-C-A g1 ***
24175469-A-C 22029322-A-C P3_b1 ***
22438133-G-A 20276247-G-A BY218504 DYZ19 ***
25153180-G-T 23007033-G-T g1 ***
26140293-A-G 23994146-A-G P1_Y1 ***
26164145-TA-T 24017998-TA-T P1_Y1 ***
26495426-TA-T 24349279-TA-T P1_Y1 ***
26722183-G-A 24576036-G-A P1_g2 ***
22447179-T-A 20285293-T-A DYZ19 ***
22312251-G-T 20150365-G-T DYZ19 ***
22327058-A-G 20165172-A-G DYZ19 ***
13480748-G-A 11325072-G-A ***
25013984-G-A 22867837-G-A g1 ***
13142999-CATTCCACTCT-C 10632485-CATTCCACTCT-C ***
6222006-A-G 6353965-A-G IR3_Dst ***
13456405-T-TCCCAC 11300729-T-TCCCAC ***
19907892-G-T 17796012-G-T P5_Prx ***
13456402-T-A 11300726-T-A ***
13456395-T-C 11300719-T-C ***
13726873-C-T 11571197-C-T ***
22225640-A-G 20063754-A-G DYZ19 ***
22230261-G-A 20068375-G-A DYZ19 ***
22248608-A-G 20086722-A-G DYZ19 ***
22258904-T-A 20097018-T-A DYZ19 ***
22261531-T-A 20099645-T-A DYZ19 ***
22266757-G-T 20104871-G-T DYZ19 ***
27001192-A-G 24855045-A-G P1_r4 ***

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.

Age Analysis Information (work in progress)

Kit: 1096631067335577409037821817
Used in age calculations1067335577409037821817
Counts of SNPs2121
Variant counts last updated 2019-11-11 02:42:07.

Big Tree Main Page