| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.1387_1661dup | p.Val463delinsValStop |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GTG | Val | ins275 | Fs. | Ins |
| 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_7722_7722-002_7722-002 | Relative |
| Symptom |
| Reference ID | Reference |
| 19 | Unpublished data |