| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.1760_2210del | p.Tyr588LeufsX7 |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GGC | Gly | del451b | Fs. | Stop at 594 | Fr. |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| EXO1 stabilization |
| At the mRNA level | On restriction map |
| New restriction site(s): none Lost restriction site(s): none |
| Sample ID | Patient status |
| 19_10086_10086-002_10086- | Relative |
| Symptom |
| Reference ID | Reference |
| 19 | Unpublished data |