| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.3412T>G | p.Cys1138Gly | Heterozygous | Mutation |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| TGT | Cys | GGT | Gly | T->G | Tv |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| cb EGF-like #13 | Disulfide bonds 1124-1138 (C4) | Yes, coding strand | No |
| At the mRNA level | On restriction map |
| NA | New restriction site(s): BsaJ I, BstU I, Dsa I, Sac II Lost restriction site(s): none |
| Conservation (0-1) | SIFT (0-1) | UMD-predictor (0-100) |
|---|---|---|
| 0.67 | 0.00 (pathogenous) | 100 (Pathogenous) |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| FRA01BOU F0149 I0188 | Proband | Male | de novo | FRANCE |
| Phenotypic group | Disease |
| NA | Classical MFS |
| Symptom | Severity |
| C-Asc. aortic dilatation | moderate |
| C-Mitral regurgitation | |
| C-Mitral valve prolapse | |
| CF-Dolichocephaly | |
| CF-Malar hypoplasia | |
| O-No implication | |
| S-Arachnodactyly (M) | |
| S-Crowding teeth (m) | |
| S-Dolichostenomelia | |
| S-Enophthalmos (m) | |
| S-High arched palate | |
| S-Joint hypermobility (m) | |
| S-Pectus carinatum (M)(2) | |
| S-Plain pes planus (M)(1) |
| Reference ID | PubMed ID | Reference |
| 64 | 12938084 | Collod-B*roud G, Le Bourdelles S, Ades L, Ala-Kokko L, Booms P, Boxer M, Child A, Comeglio P, De Paepe A, Hyland JC, Holman K, Kaitila I, Loeys B, Matyas G, Nuytinck L, Peltonen L, Rantamaki T, Robinson P, Steinmann B, Junien C, B*roud C, Boileau C. "Update of the UMD-FBN1 mutation database and creation of an FBN1 polymorphism database". Hum Mutat. 2003 Sep;22(3):199-208. |