Shoultz

FTDNA: 299727
MDKA Birth: Germany

Tree Position

R-P312/S116 > Z40481 > ZZ11 > U152/S28 > ZZ45 > Z36/S206 > Y17161 > Y16889 > A7992 > BY121456 > FGC59787

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
299727
6643707-G-A 6775666-G-A FGC75449 Y60748 YY+
6895725-AAAAC-A 7027684-AAAAC-A 4×AAAC+
7034281-T-C 7166240-T-C Y61418 FGC75451 YY+
8035769-T-C 8167728-T-C FGC59752 YY+
9013351-C-A 9175742-C-A Y64738 Y+
9761827-T-G 9924218-T-G FGC59758 Y+
14125113-GA-G 12004407-GA-G +
14472063-C-T 12351332-C-T FGC59765 YY+
14853855-A-G 12741921-A-G FGC59766 YY+
15322923-A-C 13211041-A-C FGC59768 YY+
15477382-GCTAT-G 13365502-GCTAT-G +
16680093-G-C 14568213-G-C FGC75455 Y70309 YY+
17232283-G-A 15120403-G-A Y71287 YY+
17976703-C-G 15864823-C-G FGC59776 Y+
18704392-C-A 16592512-C-A FGC75456 Y73900 YY+
18993769-G-A 16881889-G-A BY125333 YY+
19057799-C-A 16945919-C-A FGC75457 Y74532 YY+
19078393-T-C 16966513-T-C FGC75458 Y74578 YY+
19128502-T-A 17016622-T-A FGC75459 Y74715 YY+
19357402-T-G 17245522-T-G FGC59779 YY+
19410480-G-A 17298600-G-A Y75272 YY+
19522876-T-A 17410996-T-A Y75516 YY+
19522877-C-A 17410997-C-A Y75517 YY+
19522893-A-T 17411013-A-T Y75518 YY+
21312192-G-A 19150306-G-A FGC59782 YY+
21340487-C-T 19178601-C-T FGC75460 Y76288 YY+
21397610-C-T 19235724-C-T Y76398 FGC75461 YY+
21480093-A-C 19318207-A-C FGC59784 YY+
22178834-A-T 20016948-A-T FGC75462 Y77890 YY+
22271046-C-T 20109160-C-T FGC75463 DYZ19 +
22437400-A-T 20275514-A-T BY218348 DYZ19 +
23317546-T-C 21155660-T-C Y79680 FGC75465 YY+
23494275-A-G 21332389-A-G FGC75466 Y79967 YY+
23895702-T-C 21733816-T-C FGC59790 Y+
24070843-G-T 21924696-G-T FGC59791 P3_b1 +
28778128-A-C 26631981-A-C FGC75467 Y81073 +
5216025-A-G 5347984-A-G FGC59749 **
13659454-G-A 11503778-G-A FGC59762 DYZ17 **
19355428-G-T 17243548-G-T **
20306104-G-A 18144218-G-A BY212135 P5_Dst **
28705685-C-A 26559538-C-A **
10034262-C-T 10196653-C-T ***
10034263-G-T 10196654-G-T ***
22223598-G-T 20061712-G-T DYZ19 ***
22223763-T-G 20061877-T-G DYZ19 ***
6114122-G-A 6246081-G-A ***
9297833-A-G 9460224-A-G ***
9318144-A-G 9480535-A-G ***
10012583-C-G 10174974-C-G BY82888 ***
13258859-C-G 11103183-C-G BY84933 ***
13711613-G-A 11555937-G-A BY89442 DYZ17 ***
19717968-T-C 17606088-T-C P5_Prx ***
19873671-C-T 17761791-C-T P5_Prx ***
19901055-T-A 17789175-T-A P5_Prx ***
19968970-G-A 17857090-G-A P5_Prx ***
20708643-G-A 18546757-G-A P4_Prx ***
22233924-T-G 20072038-T-G DYZ19 ***
22238258-C-G 20076372-C-G DYZ19 ***
22291143-A-T 20129257-A-T DYZ19 ***
22308677-C-G 20146791-C-G DYZ19 ***
22335249-C-G 20173363-C-G DYZ19 ***
22443817-A-C 20281931-A-C BY219283 DYZ19 ***
22451904-C-T 20290018-C-T DYZ19 ***
22451908-C-T 20290022-C-T DYZ19 ***
22479414-G-A 20317528-G-A BY53244 DYZ19 ***
24201649-C-T 22055502-C-T P3_b1 ***
24827505-T-C 22681358-T-C P3_b2 ***
25761038-A-T 23614891-A-T P1_b3 ***
25857869-C-T 23711722-C-T P1_Y1 ***
25956711-G-A 23810564-G-A P1_Y1 ***

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.