Genelach Dáil Cuinn Project

Last updated: 2024 December 10

Cladogram Info

The options menu under the gear icon has the following 3 items:

Zoom In - self explanatory.
Zoom Out - self explanatory.
Horizontal or Vertical View - allows for toggling between the default vertical view similar to Alex Williamson’s The Big Tree; or a horizontal view similar to FTD’s Haplotree.

You can focus in on a particular clade by clicking on the clade name in the node. Use your browser back button to return to the previous level of view.

Hovering over a SNP name will display a small pop-up that will present the GRCh38 location of the SNP and what nucleotide(s) changed. The first letter or letter combination indicates the ancestral value(s) at that location, while the second, final set indicates the derived value(s), what the mutation changed the original value(s) to. For example, GRCh38:6911940-G-C means that at GRCh38 location 6911940 on the Y chromosome the ancestral G (guanine) nucleotide mutated to a derived C (cytosine) nucleotide.

TBD

R1b-FT63002

FT63002

FT62449

FT63314

FT103504

FT218747

R1b-FT63159

FT63159

FT62478

FT361616

Ó Mainnín?

Hannon

FTD-57443

R1b-FT361307

FT361307

FT359827

FT361241

BY11676

Ó Mainnín

Manion

FTD-B257211

Ó Mainnín

Mannion

FTD-IN132895

R1b-FTA38226

FTA38226

FTA40633

FTA42367

FTF49795

Ó Mainnín

Manion

FTD-405300

R1b-FTF14065

FTF14065

FTF13810

FTF14347

FTF14353

FTF14394

FTF14472

FTF14552

FTF14746

FTF33959

FTF34234

FTG41849

Ó Mainnín

Manion

FTD-B454245

Ó Mainnín

Mannion

FTD-IN27626

Ó Mainnín

Mannion

FTD-MK36692

R1b-FT103894

FT103894

FT104926

FT106040

MF93681

Z14094

TBT10110

Ó Mainnín

Mannion

FTD-357632