| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.830C>T | p.Pro277Leu | Heterozygous | CAUSAL |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| CCC | Pro | CTC | Leu | C->T | Ts |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Sm,NM,NMH,FA,HD | Yes, coding strand | No |
| At the mRNA level | On restriction map |
| New restriction site(s): none Lost restriction site(s): Nco I |
| Conservation (0-1) | SIFT (0-1) | UMD-predictor (0-100) |
|---|---|---|
| 0 | - | 65 (Probably pathogenous) |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of Death | Geographic origin |
| 01-DE12-S05B- | Proband | Male | 26 |
| Phenotypic group | Disease |
| Strong | Please contact curator |
| Reference ID | PubMed ID | Reference |
| 0 | Í |