| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.1357C>T | p.Gln453X | Heterozygous | CAUSAL |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| CAG | Gln | TAG | Stop | C->T | Ts |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Pem,NM,CH | No | No |
| At the mRNA level | On restriction map |
| New restriction site(s): none Lost restriction site(s): Fnu4H I |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of Death | Geographic origin |
| 04-BO19-M01R- | Proband | Female | 46 |
| Phenotypic group | Disease |
| Moderate, familial background of pituitary adenoma and hyperparathyroidism | Please contact curator |
| Reference ID | PubMed ID | Reference |
| 0 | Í |