| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.349_350ins26 | p.Leu117ArgfsX11 | Heterozygous | CAUSAL |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| CTG | Leu | ins26b | Fs. | Stop at 127 | Fr. |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Sm, NM |
| At the mRNA level | On restriction map |
| New restriction site(s): none Lost restriction site(s): none |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of Death | Geographic origin |
| 04-MU12-C01P- | Relative | Female | 0 |
| Phenotypic group | Disease |
| asymptomatic | Please contact curator |
| Reference ID | PubMed ID | Reference |
| 0 | Í |