Tree Position

A0-T-YP2191 > P305[A1] > A1b > BT/A1b2 > M168/PF1416[CT] > P143[CF] > M89/PF2746[F] > F1329/M3658[GHI > F929[HIJK] > IJK > IJ > M170[I] > Z2881 > DF29 > Z58 > Z138 > S2293 > 8129303-A-G

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	STR	BigY3 163011
26013072-A-G	23866925-A-G			P1_Y1				A*
24297789-C-T	22151642-C-T			P3_t1				A*
6234249-C-T	6366208-C-T			IR3_Dst				A*
6316734-T-C	6448693-T-C			IR3_Dst				A*
20029718-G-C	17917838-G-C			P5_Prx				A*
20737382-G-A	18575496-G-A			P4_Prx				A*
20801578-T-G	18639692-T-G			P4_Prx				A*
26368771-C-CA	24222624-C-CA			P1_Y1				A*
26482309-A-G	24336162-A-G			P1_Y1				A*
	56871132-T-C							A*
21798302-G-A	19636416-G-A	BY4236	Y32300		Y	Y		+
18833864-T-A	16721984-T-A	Y37731	Y30649		Y	Y		+
17196805-A-G	15084925-A-G				Y	Y		+
14539253-C-A	12427454-C-A		FT360483		Y	Y		+
17196807-G-A	15084927-G-A				Y	Y	5×AGAA	+
3698463-C-T	3830422-C-T		FT258530					+
3358942-C-A	3490901-C-A		FT359345					+
3615142-GATT-G	3747101-GATT-G							+
3988077-C-T	4120036-C-T		FT359452					+
5148979-C-T	5280938-C-T		FT359652					+
5374840-G-A	5506799-G-A		FT359703					+
6448221-A-G	6580180-A-G		FT359861					+
7152282-G-A	7284241-G-A		FT359966		Y	Y		+
7316338-C-T	7448297-C-T		BY13283		Y	Y		+
7316373-G-A	7448332-G-A		FT359986		Y	Y		+
8162166-C-CA	8294125-C-CA							+
8168581-A-T	8300540-A-T		FT360115		Y	Y		+
8753524-G-C	8885483-G-C		FT360216		Y	Y		+
8757983-T-C	8889942-T-C		FT360217		Y	Y		+
9171749-G-A	9334140-G-A		FT327854		Y			+
9906965-C-T	10069356-C-T		FT360320		Y			+
10022171-C-T	10184562-C-T		FT376399		Y			+
13693579-G-A	11537903-G-A		FT423924					+
13906000-C-T	11785294-C-T		FT360356		Y			+
14017116-T-A	11896410-T-A		FT360381		Y			+
14176141-T-TA	12055435-T-TA							+
14193091-C-T	12072385-C-T		FT360411		Y	Y		+
14369533-T-C	12248829-T-C		FT360451		Y	Y		+
15717026-A-G	13605146-A-G		FT360632		Y	Y		+
16198114-A-T	14086234-A-T		FT360681		Y	Y		+
16285464-T-A	14173584-T-A		FT360695		Y	Y		+
16476155-G-A	14364275-G-A		FTB36914		Y	Y		+
18118535-G-T	16006655-G-T		FT360968		Y	Y		+
18672062-A-T	16560182-A-T		FT361036		Y	Y		+
18925104-T-G	16813224-T-G		FTB37715		Y			+
19370829-G-T	17258949-G-T		FT361139		Y	Y		+
21217125-G-A	19055239-G-A		FT361186		Y	Y		+
21793000-A-T	19631114-A-T		FT361268		Y			+
21897580-T-C	19735694-T-C		FT361285		Y	Y		+
21911724-A-G	19749838-A-G		FT361288		Y	Y		+
22214061-G-A	20052175-G-A		FT361322		Y			+
22459274-T-G	20297388-T-G			DYZ19				+
22564517-G-A	20402631-G-A		FT43968		Y	Y		+
22755588-C-T	20593702-C-T		FT361363		Y	Y		+
22935817-AC-A	20773931-AC-A							+
23369723-G-A	21207837-G-A		BY144856		Y	Y		+
23775074-T-C	21613188-T-C		FT361494			Y		+
23775073-GT-G	21613187-GT-G							+
24504470-T-C	22358323-T-C		FT361542					+
18556556-C-CTGTGTG	16444676-C-CTGTGTG						15×TG	*
9533796-A-ATG	9696187-A-ATG			IR3_Prx			8×TG	*
6336567-G-GCA	6468526-G-GCA			IR3_Dst			8×CA	*
4980827-A-G	5112786-A-G							*
13447174-C-A	11291498-C-A							*
19878737-C-A	17766857-C-A			P5_Prx				*
20842594-A-C	18680708-A-C			P4_Dst				*
5235405-CTTTTTTTT-C	5367364-CTTTTTTTT-C						31×T	**
	10776140-A-T							**
	10776157-T-G							**
22483676-G-C	20321790-G-C			DYZ19				**
22483684-A-T	20321798-A-T		BY174807	DYZ19				**
13474651-T-A	11318975-T-A							**
13474732-C-G	11319056-C-G							**
22483656-G-T	20321770-G-T			DYZ19				**
28806074-G-T	26659927-G-T							**
	10776132-C-G							**
22439463-C-A	20277577-C-A			DYZ19				**
13474684-C-A	11319008-C-A							**
25858396-G-GAA	23712249-G-GAA			P1_Y1			22×A	**
2956073-T-TG	3088032-T-TG							**
4539033-T-TAAA	4670992-T-TAAA						24×A	**
7996138-C-T	8128097-C-T							**
8790304-G-C	8922263-G-C		FTB47452					**
15381497-C-A	13269617-C-A							**
15381499-G-T	13269619-G-T							**
20762245-A-C	18600359-A-C			P4_Prx				**
22273055-G-T	20111169-G-T			DYZ19				**
22439477-G-C	20277591-G-C			DYZ19				**
22439481-G-A	20277595-G-A			DYZ19				**
22483655-A-C	20321769-A-C			DYZ19				**
25912900-G-T	23766753-G-T			P1_Y1				**
28610442-CTTTT-C	26464295-CTTTT-C						21×T	***
19206741-TAAAAAA-T	17094861-TAAAAAA-T						29×A	***
15557124-AATATATAT-A,AAT	13445244-AATATATAT-A,AAT						19×AT	***
	10789389-C-G							***
23364087-C-CAA	21202201-C-CAA						16×A	***
	10893779-TTCCATTCCATTCCATTCCATTCCATTCCAT-T,TTCCATTCCATTGCATTCCAATCCATTCCAC							***
13923559-ATAT-A,AAAATAT	11802853-ATAT-A,AAAATAT							***
16290810-TAT-T,TAA	14178930-TAT-T,TAA							***
16364058-CTATATATATATATATATA-C,CTATATA	14252178-CTATATATATATATATATA-C,CTATATA						27×TA	***
18270249-CAAAAAAAAAAAAAAAA-C	16158369-CAAAAAAAAAAAAAAAA-C						35×A	***
19319834-GTATATATATATATA-G,GTATATATA	17207954-GTATATATATATATA-G,GTATATATA						23×TA	***
23293598-GTATATATATATATATA-G,GTATA	21131712-GTATATATATATATATA-G,GTATA						20×TA	***
	56887140-T-TTG,TTGT							***

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.