| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.1567G>C | p.Ala523Pro | Heterozygous | UV |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GCT | Ala | CCT | Pro | G->C | Tv |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Sm3,CH | No | No |
| At the mRNA level | On restriction map |
| New restriction site(s): BstN I, EcoR II Lost restriction site(s): none |
| Conservation (0-1) | SIFT (0-1) | UMD-predictor (0-100) |
|---|---|---|
| 0 | - | 53 (Probable polymorphism) |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of Death | Geographic origin |
| 02-LI14-M01R- | Proband | Male | 46 |
| Phenotypic group | Disease |
| Please contact curator |
| Reference ID | PubMed ID | Reference |
| 0 | Í |