P61586 (RHOA) at position 25
Download results as CSV19 mutations found: 8 benign and 11 pathogenic.
D2Deep score mean: 0.585. Overall confidence mean: 0.425
| Identifier | Original | Position | Target | D2Deep Prediction | Pred. Interpretation | Overall confidence | Actions |
|---|---|---|---|---|---|---|---|
| F25A | F | 25 | A | 0.424 | Benign based on D2Deep prediction | 0.824 | View mutation |
| F25C | F | 25 | C | 0.447 | Benign based on D2Deep prediction | 0.824 | View mutation |
| F25D | F | 25 | D | 0.932 | Pathogenic based on D2Deep prediction | 0.136 | View mutation |
| F25E | F | 25 | E | 0.950 | Pathogenic based on D2Deep prediction | 0.136 | View mutation |
| F25G | F | 25 | G | 0.991 | Pathogenic based on D2Deep prediction | 0.136 | View mutation |
| F25H | F | 25 | H | 0.966 | Pathogenic based on D2Deep prediction | 0.136 | View mutation |
| F25I | F | 25 | I | 0.012 | Benign based on D2Deep prediction | 0.824 | View mutation |
| F25K | F | 25 | K | 0.993 | Pathogenic based on D2Deep prediction | 0.136 | View mutation |
| F25L | F | 25 | L | 0.011 | Benign based on D2Deep prediction | 0.824 | View mutation |
| F25M | F | 25 | M | 0.068 | Benign based on D2Deep prediction | 0.824 | View mutation |
| F25N | F | 25 | N | 0.837 | Pathogenic based on D2Deep prediction | 0.136 | View mutation |
| F25P | F | 25 | P | 0.999 | Pathogenic based on D2Deep prediction | 0.136 | View mutation |
| F25Q | F | 25 | Q | 0.709 | Pathogenic based on D2Deep prediction | 0.136 | View mutation |
| F25R | F | 25 | R | 0.961 | Pathogenic based on D2Deep prediction | 0.136 | View mutation |
| F25S | F | 25 | S | 0.158 | Benign based on D2Deep prediction | 0.824 | View mutation |
| F25T | F | 25 | T | 0.599 | Pathogenic based on D2Deep prediction | 0.136 | View mutation |
| F25V | F | 25 | V | 0.068 | Benign based on D2Deep prediction | 0.824 | View mutation |
| F25W | F | 25 | W | 0.992 | Pathogenic based on D2Deep prediction | 0.136 | View mutation |
| F25Y | F | 25 | Y | 0.003 | Benign based on D2Deep prediction | 0.824 | View mutation |