| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.4766G>T | p.Cys1589Phe | Heterozygous | Mutation |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| TGT | Cys | TTT | Phe | G->T | Tv |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| TGFBP#04 | C in disulfide bonds 1564-1589 | No | No |
| At the mRNA level | On restriction map |
| NA | New restriction site(s): none Lost restriction site(s): none |
| Conservation (0-1) | SIFT (0-1) | UMD-predictor (0-100) |
|---|---|---|
| 1 | 0.00 (pathogenous) | 100 (Pathogenous) |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| USA03STA F0004 I880 | Proband | Male | de novo | U.S.A |
| Phenotypic group | Disease |
| Type V | Classical MFS |
| Symptom | Severity |
| C-Asc. aortic dilatation | surgery |
| C-Asc. aortic dilatation | |
| C-Mitral valve prolapse | |
| C-Tricuspid valve prolapse | |
| O-Ectopia lentis | |
| O-Myopia | |
| S-Abnormal ears | |
| S-Crowding teeth (m) | |
| S-High arched palate | |
| S-Joint limitations |
| Reference ID | PubMed ID | Reference |
| 12 | 8281141 | Tynan K, Comeau K, Pearson M, Wilgenbus P, Levitt D, Gasner C, Berg MA, Miller DC, Francke U. "Mutation screening of complete fibrillin-1 coding sequence: report of five new mutations, including two in 8-cysteine domains". Hum Mol Genet 1993 Nov;2(11):1813-21 . |