Colangelo

BigY3: 223929
MDKA Birth: Italy > Basilicata 1880

Tree Position

R-P312/S116 > Z40481 > ZZ11 > U152/S28 > Z193

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
223929
23715727-C-T 21553841-C-T A*
14465752-A-C 12345025-A-C YYA*
6260972-T-C 6392931-T-C IR3_Dst A*
6334854-T-G 6466813-T-G IR3_Dst A*
16110981-A-C 13999101-A-C P8_Prx A*
18287350-A-G 16175470-A-G P6_Prx A*
18319340-A-G 16207460-A-G P6_Prx A*
19620862-A-G 17508982-A-G P5_Prx YA*
19792704-C-A 17680824-C-A P5_Prx A*
20667159-T-C 18505273-T-C P4_Prx A*
20785734-G-C 18623848-G-C P4_Prx A*
22291086-G-A 20129200-G-A DYZ19 A*
23174781-A-G 21012895-A-G YA*
26065951-A-T 23919804-A-T P1_Y1 A*
21777179-C-T 19615293-C-T BY135381 YY+
13194830-C-A 11039154-C-A FT440473 +
3311104-A-G 3443063-A-G FT214165 +
4073243-G-A 4205202-G-A FT214441 +
4076043-G-T 4208002-G-T FT214443 +
4568341-TATTTC-T 4700300-TATTTC-T +
5041975-C-G 5173934-C-G FT214761 +
5485781-T-TA 5617740-T-TA 9×A+
5594632-T-G 5726591-T-G FT214992 +
5659923-A-G 5791882-A-G FT215016 +
6136115-A-G 6268074-A-G FT215189 +
6962037-A-G 7093996-A-G FT215389 YY+
7540760-C-G 7672719-C-G FT215544 YY+
7707522-G-T 7839481-G-T FT215595 YY+
7822436-G-A 7954395-G-A FT215631 YY+
7936903-A-G 8068862-A-G FT215667 YY+
8423848-A-G 8555807-A-G FT215789 YY+
8737786-T-C 8869745-T-C FT215895 YY+
9915525-T-C 10077916-T-C FT333189 Y+
10039674-G-A 10202065-G-A FT376774 +
10793708-A-G FT431454 +
13815726-AGGAAT-A 11695020-AGGAAT-A 4×GGAAT+
14042146-C-A 11921440-C-A FT216235 YY+
14627688-T-C 12515756-T-C FT216438 YY+
15965529-A-G 13853649-A-G FT216795 YY+
16819996-C-A 14708116-C-A FT217048 YY+
16838162-A-T 14726282-A-T FT217057 YY+
17279001-G-T 15167121-G-T FT217174 YY+
17572787-C-A 15460907-C-A FT217269 YY+
17867332-TAAC-T 15755452-TAAC-T +
18581693-G-A 16469813-G-A FT217515 YY+
18672169-T-A 16560289-T-A FT217546 YY+
18755322-C-T 16643442-C-T YY+
18909605-A-G 16797725-A-G FT217595 YY+
19172049-ATAT-A 17060169-ATAT-A +
21246234-C-G 19084348-C-G FT217879 Y+
21456540-G-A 19294654-G-A FT217940 YY+
22476420-T-A 20314534-T-A FT459859 DYZ19 +
23293033-C-A 21131147-C-A FT218424 YY+
23363509-C-T 21201623-C-T FT218437 Y+
23784986-G-A 21623100-G-A FT218537 Y+
24872754-G-T 22726607-G-T FT461031 IR1_R +
13842646-CGGAATGGAATGGAAT-C 11721940-CGGAATGGAATGGAAT-C 12×GGAAT*
10983043-C-CTCCAT *
13467563-C-T 11311887-C-T BY85773 **
9732827-G-A 9895218-G-A IR3_Prx **
4229243-G-A 4361202-G-A **
6338084-A-AG 6470043-A-AG IR3_Dst **
13467534-G-T 11311858-G-T **
13467595-A-G 11311919-A-G **
14213672-GA-G 12092966-GA-G **
14661454-G-T 12549519-G-T **
16031357-G-GAT 13919477-G-GAT **
18195123-G-T 16083243-G-T **
20084146-GAGA-G 17972266-GAGA-G P5_Dst **
20123768-T-C 18011888-T-C P5_Dst **
20123771-G-A 18011891-G-A P5_Dst **
20559296-A-AAAT 18397410-A-AAAT P5_Dst **
21599252-G-GAA 19437366-G-GAA 11×A**
21955211-G-A 19793325-G-A **
22446013-G-C 20284127-G-C FT457088 DYZ19 **
22446238-G-A 20284352-G-A DYZ19 **
22468567-T-C 20306681-T-C DYZ19 **
23052262-T-A 20890376-T-A **
24871182-A-G 22725035-A-G IR1_R ***
25866495-C-CA 23720348-C-CA P1_Y1 10×A***
18872339-G-T 16760459-G-T ***
4389404-CAAAAA-C 4521363-CAAAAA-C 21×A***
14771126-C-CTT 12659195-C-CTT 16×T***
8321435-CT-C,CTTT 8453394-CT-C,CTTT 15×T***
10988581-ACTC-A ***
13450110-TCCACCCCATCCCATC-T,TCCATTCCATTCCATG 11294434-TCCACCCCATCCCATC-T,TCCATTCCATTCCATG ***
14888076-CT-C,CTT 12776142-CT-C,CTT 17×T***
6147534-C-T 6279493-C-T IR3_Dst ***
9524019-GTATATA-G,GTATA 9686410-GTATATA-G,GTATA 21×TA***
14203430-CAAAAAA-C,CAAAAAAA 12082724-CAAAAAA-C,CAAAAAAA 23×A***
16031357-G-T 13919477-G-T ***
16408114-CCACA-C,CCA 14296234-CCACA-C,CCA 19×CA***
16727367-G-T 14615487-G-T ***
20574944-G-GT,GTT 18413058-G-GT,GTT P5_Dst 19×T***
21515901-C-A 19354015-C-A ***
28700833-T-C 26554686-T-C ***

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.