| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.1502_1510del | p.Asp501_Leu504delinsVal | Heterozygous | LIKELY CAUSAL |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GAC | Asp | del9b | InF | In frame del | InF |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Sm3,CH |
| Other variation(s) reported for this sample: c.143T>C |
| 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 |
| 03-PE19-J15H- | Relative | Male | 34 |
| Phenotypic group | Disease |
| Moderate | Please contact curator |
| Reference ID | PubMed ID | Reference |
| 0 | Í |