Rayner

BigY3: B215075
MDKA Birth: England

Tree Position

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

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 STRBigY3
B215075
13449582-C-G 11293906-C-G A*
18361328-G-A 16249448-G-A P6_Prx A*
19584720-A-T 17472840-A-T P5_Prx YA*
20002076-C-T 17890196-C-T P5_Prx A*
20763732-A-G 18601846-A-G P4_Prx A*
22307883-T-C 20145997-T-C DYZ19 A*
24297487-G-A 22151340-G-A P3_t1 A*
25618791-A-T 23472644-A-T P1_gr1 A*
26164557-T-C 24018410-T-C P1_Y1 A*
26336088-C-T 24189941-C-T P1_Y1 A*
56837072-A-G A*
3879340-G-A 4011299-G-A +
20066492-A-T 17954612-A-T P5_Gap +
7231012-A-T 7362971-A-T FT241993 YY+
5949490-C-T 6081449-C-T FT18190 +
3083424-T-C 3215383-T-C FT240998 +
3119312-C-G 3251271-C-G +
3357460-G-A 3489419-G-A FT241062 +
3477506-CCT-C 3609465-CCT-C +
3711050-TA-T 3843009-TA-T +
3849622-G-T 3981581-G-T FT241191 +
3853617-A-C 3985576-A-C +
4386953-CTATG-C 4518912-CTATG-C +
4580820-A-G 4712779-A-G FT241376 +
5068667-G-A 5200626-G-A +
5292203-TTTAA-T 5424162-TTTAA-T +
5426744-A-G 5558703-A-G FT241602 +
6657308-C-A 6789267-C-A FT241871 YY+
6657480-G-C 6789439-G-C FT241872 YY+
6990078-A-G 7122037-A-G FT241946 YY+
7182887-A-T 7314846-A-T FT241979 YY+
7689227-C-A 7821186-C-A FT242084 YY+
7840016-A-C 7971975-A-C FT280737 YY+
8075144-CA-C 8207103-CA-C +
8085061-C-G 8217020-C-G YY+
8309170-A-C 8441129-A-C FT242215 YY+
8577829-C-T 8709788-C-T FT242291 YY+
8583326-T-C 8715285-T-C YY+
10794405-C-T FT431482 +
10887008-TTCCATTCCAC-T +
14382584-G-A 12261880-G-A FT81896 Y+
14923426-C-T 12811491-C-T FT242838 YY+
15224709-G-A 13112795-G-A FT242899 Y+
15224710-G-A 13112796-G-A FT242900 Y+
15224713-A-G 13112799-A-G FT242901 Y+
15261279-A-G 13149363-A-G FT242906 YY+
15381635-T-G 13269755-T-G FT242928 YY+
15574190-TTTTA-T 13462310-TTTTA-T +
15757524-A-C 13645644-A-C FT243023 YY+
16260362-G-C 14148482-G-C YY+
16563025-G-A 14451145-G-A FT243195 YY+
16835239-G-A 14723359-G-A YY+
16851267-G-C 14739387-G-C YY+
17570450-A-G 15458570-A-G YY+
18526710-G-T 16414830-G-T FT243624 P6_Dst +
18829308-G-T 16717428-G-T FT243704 YY+
19526102-G-A 17414222-G-A YY+
21140575-CGCAGCCTCTCA-C 18978689-CGCAGCCTCTCA-C +
22060120-T-C 19898234-T-C Y+
23238254-C-A 21076368-C-A FT244307 Y+
23729570-A-T 21567684-A-T FT244384 +
3663021-A-G 3794980-A-G PF54 *
3663022-T-C 3794981-T-C FT27339FGC45675 *
3663032-T-C 3794991-T-C Y60549 *
5549533-A-C 5681492-A-C *
23296051-G-GT 21134165-G-GT 9×T*
22562599-T-G 20400713-T-G A8005 **
17926534-CAAAA-C 15814654-CAAAA-C 25×A**
15325006-TTAAATAAA-T 13213124-TTAAATAAA-T 7×TAAA**
4634602-AATAT-A 4766561-AATAT-A 9×AT**
28581630-G-GATATAT 26435483-G-GATATAT 19×AT**
22476168-A-T 20314282-A-T FGC9336 FGC49877 DYZ19 **
26246524-A-G 24100377-A-G P1_Y1 **
18035665-CTTTTTTTT-C 15923785-CTTTTTTTT-C 30×T**
25647132-TG-T 23500985-TG-T P1_b3 **
25647130-A-AC 23500983-A-AC P1_b3 **
3321016-T-C 3452975-T-C **
3584974-T-C 3716933-T-C **
5201808-T-A 5333767-T-A **
5588384-T-A 5720343-T-A **
5872977-G-C 6004936-G-C **
8379253-C-A 8511212-C-A **
13441556-A-G 11285880-A-G **
13984954-T-C 11864248-T-C FTA49842 **
14161456-G-GA 12040750-G-GA **
14964737-C-T 12852812-C-T **
15224706-G-GAAAAGTA 13112792-G-GAAAAGTA **
15402726-T-C 13290846-T-C **
15490546-T-G 13378666-T-G **
15576950-A-G 13465070-A-G **
18125759-GGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA-G 16013879-GGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAA-G 13×GAAA**
21123427-CATGCTT-C 18961541-CATGCTT-C **
22270143-C-T 20108257-C-T DYZ19 **
22486990-G-T 20325104-G-T BY48658 DYZ19 **
22538193-T-A 20376307-T-A **
24252249-A-G 22106102-A-G P3_b1 **
25647117-T-A 23500970-T-A P1_b3 **
26337096-T-C 24190949-T-C P1_Y1 **
27506375-A-AG 25360228-A-AG P1_Y2 **
28543264-T-C 26397117-T-C **
22255710-C-T 20093824-C-T DYZ19 ***
13223501-G-GGAA 11067825-G-GGAA ***
24466049-T-C 22319902-T-C Y35065 ***
17419439-ATTTTTTTTT-A 15307559-ATTTTTTTTT-A 25×T***
13456837-TATTCCATTCCATTCC-T 11301161-TATTCCATTCCATTCC-T 7×ATTCC***
14025974-G-A 11905268-G-A ***
14025976-A-AG 11905270-A-AG ***
14776923-CA-C,CAA 12664992-CA-C,CAA 15×A***
3637480-T-G 3769439-T-G ***
4264677-G-T 4396636-G-T ***
5231121-T-C 5363080-T-C ***
5586587-T-C 5718546-T-C ***
8274006-T-C 8405965-T-C ***
13588522-TA-T 11432846-TA-T ***
15623177-T-A 13511297-T-A ***
17030992-CAAAAA-C,CAAA 14919112-CAAAAA-C,CAAA 19×A***
17942122-T-A 15830242-T-A ***
18095725-A-G 15983845-A-G ***
18630934-T-C 16519054-T-C ***
21062118-A-G 18900232-A-G ***
22228239-C-G 20066353-C-G DYZ19 ***
22280109-A-T 20118223-A-T DYZ19 ***
22281293-C-T 20119407-C-T DYZ19 ***
21757617-C-T ***
24666428-A-G 22520281-A-G P3_b2 ***
28602617-T-C 26456470-T-C ***
28602618-G-A 26456471-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.