Knowledge graph · Variant
PAX5 P80R
SNV
- Identifier
- CI-VAR-00003408
- Entity page
- /variant/pax5-p80r ↗
- Edges
- 2
- Neighbours
- 1 cancers
- Drawn
- 1 of 1 neighbours (cap 60); table lists every fetched edge
Accepted: cancer:<slug>, gene:<symbol>, variant:<slug>, drug:<slug>, trial:<NCT id>, or a bare CI id. Find slugs with search.
Most connectedLung Non-Small Cell Carcinoma 3,149Malignant Colorectal Neoplasm 1,866ABL1 298EGFR 276Imatinib 450Dasatinib 321
Neighbourhood
Radial view
Focus at the centre; neighbours grouped by entity type. Click a node to re-centre the graph on it; ↗ opens the entity page. Hover a spoke for relationship, evidence level, cancer context and source.
Edges
Every edge, grouped by relationship
Source-native edges first (aggregated per neighbour, direction, evidence level and source), then derived registry links. Up to 15 per relationship (10 trials); “show all” raises one group to 200.
| Relationship | Neighbour | Direction | Evidence level | Cancer context | Support | Claim | Source | Expand |
|---|---|---|---|---|---|---|---|---|
| PAX5 P80R diagnostic of …DIAGNOSTIC_OF1 of 1 | ||||||||
| → diagnostic of | B Acute Lymphoblastic Leukemia with PAX5 P80R Mutationmolecular_subtype 3 source records aggregated | supports | B | B Acute Lymphoblastic Leukemia with PAX5 P80R Mutation | 3 | Curated | civic | graph → |
| PAX5 P80R has curated evidence in … | ||||||||