| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.466G>T | p.Gly156Cys | Heterozygous | LIKELY CAUSAL |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GGT | Gly | TGT | Cys | G->T | Tv |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Ju,Sm,NMH,HD,NM | Yes, non coding strand | No |
| At the mRNA level | On restriction map |
| New restriction site(s): AlwN I Lost restriction site(s): Hpa II, Msp I |
| Conservation (0-1) | SIFT (0-1) | UMD-predictor (0-100) |
|---|---|---|
| 0 | - | 82 (Pathogenous) |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of Death | Geographic origin |
| 03-DA22-A12E- | Proband | Female | 18 |
| Phenotypic group | Disease |
| Please contact curator |
| Reference ID | PubMed ID | Reference |
| 39 | 17623761 | Clinical Testing for Mutations in the MEN1 Gene in Sweden: A Report on 200 Unrelated Cases Emma Tham, Ulla Grandell, Eva Lindgren, G*ran Toss, Britt Skogseid, and Magnus Nordenskj*ld The Journal of Clinical Endocrinology & Metabolism 2007 92:9, 3389-3395 |