| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.1665T>G | p.Ser555Arg | Heterozygous | LIKELY CAUSAL |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| AGT | Ser | AGG | Arg | T->G | Tv |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Sm3,CH | No | No |
| At the mRNA level | On restriction map |
| New restriction site(s): none Lost restriction site(s): none |
| Conservation (0-1) | SIFT (0-1) | UMD-predictor (0-100) |
|---|---|---|
| 0 | - | 71 (Probably pathogenous) |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of Death | Geographic origin |
| 03-PO09-A14N- | Relative | Female | 28 |
| Phenotypic group | Disease |
| Moderate | 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 |