| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.1485dup | p.Lys496GlnfsX35 | Heterozygous | CAUSAL |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| AAG | Lys | ins1a | Fs. | Stop at 530 | 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 |
| 03-ME25-P01T- | Proband | Female | 17 |
| Phenotypic group | Disease |
| Please contact curator |
| Reference ID | PubMed ID | Reference |
| 3 | 11836268 | Verg*s, B., Boureille, F., Goudet, P., Murat, A., Beckers, A., Sassolas, G., ? Calender, A. (2002). Pituitary disease in MEN type 1 (MEN1): data from the France-Belgium MEN1 multicenter study. The Journal of Clinical Endocrinology and Metabolism, 87(2), 457?65. doi:10.1210/jcem.87.2.8145 |