| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.1174G>T | p.Glu392X | Heterozygous | CAUSAL |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GAG | Glu | TAG | Stop | G->T | Tv |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Ju,Pem,NM,RP,FA,HD | Yes, non coding strand | No |
| 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-MA18-A20E- | Relative | Female |
| Phenotypic group | Disease |
| asymptomatic | Please contact curator |
| Reference ID | PubMed ID | Reference |
| 28 | 10534569 | Germline mutations in the MEN1 gene: creation of a new splice acceptor site and insertion of 7 intron nucleotides into the mRNA. Engelbach M1, Forst T, Hankeln T, Tratzky M, Heerdt S, PfŸtzner A, Kann P, Kunt T, Schneider S, Schmidt ER, Beyer J. |