Tree Position

R-P312/S116 > DF19/S232 > Z302/S233 > FT11655 > Z8193

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
6382888-G-A 6514847-G-A BY59994 +
17320022-A-G 15208142-A-G M9996 F4366 Z39846 YY+
21359645-G-T 19197759-G-T Z24593 Z39853 YY+
7052085-GA-G 7184044-GA-G +
7232444-C-T 7364403-C-T Z39831 YY+
7737381-A-T 7869340-A-T Z39832 YY+
8068811-C-G 8200770-C-G Z39833 YY+
8090386-T-C 8222345-T-C Z39834 YY+
8310483-A-G 8442442-A-G Z39835 YY+
8416325-C-T 8548284-C-T BY72491 YY+
8831926-T-C 8963885-T-C Z39836 YY+
9399792-C-T 9562183-C-T Z39837 YY+
13850430-T-C 11729724-T-C BY43277 +
14263817-A-G 12143111-A-G Z39838 YY+
14497707-C-T 12385912-C-T Z39839 YY+
14843915-C-G 12731981-C-G Z39840 YY+
15437496-A-T 13325616-A-T Z39842 YY+
15682543-A-G 13570663-A-G Z39843 YY+
15829191-G-T 13717311-G-T Z39844 YY+
15970220-A-G 13858340-A-G Z39845 YY+
16239048-C-G 14127168-C-G BY106253 YY+
17892360-A-G 15780480-A-G Z39847 YY+
18206046-T-A 16094166-T-A Z39848 YY+
18422296-A-G 16310416-A-G Z39849 P6_Gap +
19093263-G-A 16981383-G-A Z39850 YY+
19272958-A-G 17161078-A-G Z39851 YY+
19477952-G-T 17366072-G-T Z39852 YY+
21384556-C-T 19222670-C-T Z39854 YY+
21542396-T-C 19380510-T-C Z39855 YY+
21723695-C-T 19561809-C-T Z39856 YY+
22444779-C-T 20282893-C-T Z39857 DYZ19 +
22514278-A-G 20352392-A-G Z39858 Y+
22845110-A-T 20683224-A-T Z39859 YY+
23498854-T-C 21336968-T-C Z39860 YY+
23989618-G-C 21843471-G-C Z39861 Y+
18763630-A-C 16651750-A-C **
17683950-C-T 15572070-C-T CTS7817 M4248 **
24130397-C-A 21984250-C-A P3_b1 **
17683951-C-G 15572071-C-G CTS7818 M4085 **
8379062-C-A 8511021-C-A F126 **
24405646-G-A 22259499-G-A BY44221 **
58979931-T-C 56833784-T-C ***
13801547-T-A,C 11680841-T-A,C ***
58979917-T-G 56833770-T-G ***
13735936-G-C 11580260-G-C ***
13863328-C-T 11742622-C-T BY43285 ***
19585972-A-G 17474092-A-G P5_Prx ***
20621446-T-C 18459560-T-C P4_Prx ***
20623112-T-A 18461226-T-A P4_Prx ***
20626140-A-C 18464254-A-C P4_Prx ***
20673709-A-G 18511823-A-G P4_Prx ***
22238598-T-C 20076712-T-C DYZ19 ***
22248542-C-T 20086656-C-T DYZ19 ***
24154276-C-T 22008129-C-T P3_b1 ***
24161034-A-T 22014887-A-T P3_b1 ***
24908124-T-C 22761977-T-C g1 ***
25247161-C-T 23101014-C-T P2_r1 ***
25887287-A-C 23741140-A-C P1_Y1 ***
25962081-A-G 23815934-A-G P1_Y1 ***
26397578-TA-T 24251431-TA-T P1_Y1 9×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.