Blanton

BigY3: 962308
MDKA Birth: France > Grand Est 1550

Tree Position

R-P312/S116 > Z40481 > ZZ11 > DF27/S250 > Z195/S355 > Z272 > S450 > Z295/S1217 > S25783 > CTS4065 > 15548847GACAC-G > A5001 > FGC69210 > 6520346-C-T

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
962308
21177056-T-TTA 19015170-T-TTA 11×TAA*
3154138-T-G 3286097-T-G A*
22996968-G-T 20835082-G-T YYA*
6163554-C-CT 6295513-C-CT IR3_Dst 9×TA*
13462197-C-T 11306521-C-T A*
8126309-A-T 8258268-A-T YYA*
17067891-G-GA 14956011-G-GA 9×AA*
28817614-C-T 26671467-C-T A*
16103638-A-T 13991758-A-T P8_Prx A*
19826539-A-G 17714659-A-G P5_Prx A*
20674210-G-T 18512324-G-T P4_Prx A*
25899087-C-T 23752940-C-T P1_Y1 A*
25935220-G-A 23789073-G-A P1_Y1 A*
27617905-G-A 25471758-G-A P1_Y2 A*
18945713-C-T 16833833-C-T BY3226A7786 YY+
5601167-A-C 5733126-A-C FT263432 +
17029300-G-A 14917420-G-A FT30413 YY+
3905661-C-T 4037620-C-T FT263190 +
4252763-AC-A 4384722-AC-A +
4935149-A-C 5067108-A-C FT263338 +
5155153-T-C 5287112-T-C FT263368 +
5227823-T-G 5359782-T-G FT263379 +
5836223-A-G 5968182-A-G FT263468 +
6520958-T-C 6652917-T-C FT263554 +
6653264-C-G 6785223-C-G FT263563 YY+
6773295-A-G 6905254-A-G FT263573 Y+
6788697-G-A 6920656-G-A FTB41068 YY+
7271998-T-C 7403957-T-C FTB41111 YY+
7741535-T-G 7873494-T-G FT263697 YY+
8772592-G-A 8904551-G-A FT263816 YY+
10831217-C-T +
13421674-T-C 11265998-T-C FT443579 +
13528003-C-T 11372327-C-T FT444762 +
14553848-A-G 12442049-A-G FT264043 YY+
15219536-A-G 13107622-A-G FT264116 Y+
15491153-A-T 13379273-A-T FT264151 YY+
15914152-T-G 13802272-T-G FTB41471 YY+
16529082-A-G 14417202-A-G FT264262 YY+
16982387-G-A 14870507-G-A FT264313 YY+
16987697-T-A 14875817-T-A FT264314 YY+
17146636-A-T 15034756-A-T FTB11557 YY+
18059031-T-C 15947151-T-C FT264472 Y+
18726156-G-A 16614276-G-A FT264543 YY+
19073228-A-G 16961348-A-G FT264589 YY+
19348045-G-T 17236165-G-T FT264628 YY+
21194578-A-G 19032692-A-G FT264680 YY+
21287687-C-T 19125801-C-T FT264696 YY+
21496607-G-C 19334721-G-C FT264726 Y+
21990507-A-T 19828621-A-T FT264787 YY+
22228428-G-A 20066542-G-A FT453082 DYZ19 +
22229076-A-C 20067190-A-C DYZ19 +
24472757-T-G 22326610-T-G FT264988 Y+
22317365-T-C 20155479-T-C DYZ19 *
20557658-TG-T 18395772-TG-T P5_Dst *
3719844-A-G 3851803-A-G FTB16190 *
4424376-TG-T,TT 4556335-TG-T,TT *
4811249-A-ACAT 4943208-A-ACAT *
22320063-G-C 20158177-G-C DYZ19 *
25883669-C-T 23737522-C-T P1_Y1 11×T**
20994356-AAAAG-A 18832470-AAAAG-A P4_Dst 4×AAAG**
10834415-GCATTC-G **
20775175-GA-G 18613289-GA-G P4_Prx 10×A**
26124493-G-T 23978346-G-T P1_Y1 **
25934375-T-TAA 23788228-T-TAA P1_Y1 17×A**
20692990-C-A 18531104-C-A P4_Prx **
26060214-AAG-A 23914067-AAG-A P1_Y1 **
23199780-C-A 21037894-C-A **
20948671-GT-G 18786785-GT-G P4_Dst **
18316564-T-G 16204684-T-G P6_Prx **
26293530-AT-A 24147383-AT-A P1_Y1 **
26244879-C-A 24098732-C-A P1_Y1 **
2679124-T-C 2811083-T-C **
4427613-T-C 4559572-T-C **
4427630-G-A 4559589-G-A **
9888052-T-C 10050443-T-C FTB16969 **
13251462-C-A 11095786-C-A **
19914422-A-G 17802542-A-G P5_Prx **
22253614-T-A 20091728-T-A DYZ19 **
22316131-T-C 20154245-T-C DYZ19 **
25566715-T-G 23420568-T-G P1_gr1 **
13476960-A-C 11321284-A-C ***
18395723-TTATATATATATA-T 16283843-TTATATATATATA-T P6_Gap 27×TA***
13448640-ATTCCATTCCATTCCATTCCAT-A,ATCCATTCCATTCCATTCCAT 11292964-ATTCCATTCCATTCCATTCCAT-A,ATCCATTCCATTCCATTCCAT ***
28594590-T-TTG 26448443-T-TTG 10×TG***
8126304-A-T 8258263-A-T ***
15834190-T-C 13722310-T-C ***
6699020-ATTTTT-A 6830979-ATTTTT-A 24×T***
19146569-CTTTTTT-C,CTTTTT 17034689-CTTTTTT-C,CTTTTT 28×T***
15045161-T-G 12933251-T-G ***
3259035-CAA-C,CAAA 3390994-CAA-C,CAAA 22×A***
14075637-A-C 11954931-A-C ***
4826400-TTATA-T,TTA 4958359-TTATA-T,TTA 22×TA***
7573145-CAAA-C,CAAAA 7705104-CAAA-C,CAAAA 22×A***
13257285-ATATA-A,AT 11101609-ATATA-A,AT ***
22420083-A-T 20258197-A-T FT455943 DYZ19 ***

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.