| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.1545_1546insg | p.Arg516AlafsX15 | Heterozygous | CAUSAL |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| CGG | Arg | ins1a | Fs. | Stop at 530 | Fr. |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Sm3,CH | Yes, coding strand |
| At the mRNA level | On restriction map |
| New restriction site(s): BsaJ I Lost restriction site(s): Bcn I, BstN I, EcoO109 I, EcoR II, Hpa II, Msp I, Nci I, Nla IV, Sau96 I |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of Death | Geographic origin |
| 03-MA18-P09E- | Relative | Male | 46 |
| Phenotypic group | Disease |
| Not available | Please contact curator |
| Reference ID | PubMed ID | Reference |
| 21 | 15635078 | Medical genetics in practice: A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testing J W Cardinal, L Bergman, N Hayward, A Sweet, J Warner, L Marks, D Learoyd, T Dwight, B Robinson, M Epstein, M Smith, B T Teh, D P Cameron, J B Prins J Med Genet 2005;42:1 69-74 doi:10.1136/jmg.2003.017319 |