P40259 (CD79B) at position 25
Download results as CSV19 mutations found: 7 benign and 12 pathogenic.
D2Deep score mean: 0.545. Overall confidence mean: 0.371
| Identifier | Original | Position | Target | D2Deep Prediction | Pred. Interpretation | Overall confidence | Actions |
|---|---|---|---|---|---|---|---|
| P25A | P | 25 | A | 0.981 | Pathogenic based on D2Deep prediction | 0.018 | View mutation |
| P25C | P | 25 | C | 0.694 | Pathogenic based on D2Deep prediction | 0.018 | View mutation |
| P25D | P | 25 | D | 0.748 | Pathogenic based on D2Deep prediction | 0.018 | View mutation |
| P25E | P | 25 | E | 0.159 | Benign based on D2Deep prediction | 0.976 | View mutation |
| P25F | P | 25 | F | 0.953 | Pathogenic based on D2Deep prediction | 0.018 | View mutation |
| P25G | P | 25 | G | 0.041 | Benign based on D2Deep prediction | 0.976 | View mutation |
| P25H | P | 25 | H | 0.676 | Pathogenic based on D2Deep prediction | 0.018 | View mutation |
| P25I | P | 25 | I | 0.087 | Benign based on D2Deep prediction | 0.976 | View mutation |
| P25K | P | 25 | K | 0.584 | Pathogenic based on D2Deep prediction | 0.018 | View mutation |
| P25L | P | 25 | L | 0.972 | Pathogenic based on D2Deep prediction | 0.018 | View mutation |
| P25M | P | 25 | M | 0.569 | Pathogenic based on D2Deep prediction | 0.018 | View mutation |
| P25N | P | 25 | N | 0.265 | Benign based on D2Deep prediction | 0.976 | View mutation |
| P25Q | P | 25 | Q | 0.292 | Benign based on D2Deep prediction | 0.976 | View mutation |
| P25R | P | 25 | R | 0.845 | Pathogenic based on D2Deep prediction | 0.018 | View mutation |
| P25S | P | 25 | S | 0.058 | Benign based on D2Deep prediction | 0.976 | View mutation |
| P25T | P | 25 | T | 0.027 | Benign based on D2Deep prediction | 0.976 | View mutation |
| P25V | P | 25 | V | 0.865 | Pathogenic based on D2Deep prediction | 0.018 | View mutation |
| P25W | P | 25 | W | 0.960 | Pathogenic based on D2Deep prediction | 0.018 | View mutation |
| P25Y | P | 25 | Y | 0.573 | Pathogenic based on D2Deep prediction | 0.018 | View mutation |