| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.1387_1405dup | p.Pro469ArgfsX16 |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GGA | Gly | ins19a | Fs. | Stop at 484 | Fr. |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| EXO1 interaction |
| At the mRNA level | On restriction map |
| New restriction site(s): none Lost restriction site(s): none |
| Sample ID | Patient status |
| 71_-3242G05137 | Proband |
| Symptom |
| Reference ID | Reference |
| 71 | Unpublished data |