| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.1539_1540delAC | p.Arg516GlufsX14 | Heterozygous | CAUSAL |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GGA | Gly | del2c | Fs. | Stop at 529 | Fr. |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Sm3,CH |
| 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-BO14-V01L- | Relative | Female | 48 |
| Phenotypic group | Disease |
| father:hyperparathyroidism | Please contact curator |
| Reference ID | PubMed ID | Reference |
| 0 | Í |