| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.412dup | p.Ala138GlyfsX42 | Heterozygous | CAUSAL |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GCC | Ala | ins1b | Fs. | Stop at 179 | 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 |
| 01-PA18-N09C- | Proband | Male | 25 |
| Phenotypic group | Disease |
| Please contact curator |
| Reference ID | PubMed ID | Reference |
| 0 | Í |