| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.1080ins12 | p.Ile360delinsIleThrLysAsnSer | Heterozygous | LIKELY CAUSAL |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| ATC | Ile | ins12c | InF | In frame ins | Fr. |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Ju,NF,Pem,NM,RP,FA,HD |
| 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-ME18-N09C- | Proband | Male | 37 |
| Phenotypic group | Disease |
| Strong | Please contact curator |
| Reference ID | PubMed ID | Reference |
| 0 | Í |