| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.1347dup | p.Asp450GlyfsX29 |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GAT | Asp | ins1a | Fs. | Stop at 478 |
| 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 |
| 14_FONT_LE_COM_05C247_05C | Relative |
| Symptom |
| Reference ID | Reference |
| 14 | Unpublished data |