| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.4621C>T | p.Arg1541X | Heterozygous | Mutation |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| CGA | Arg | TGA | Stop | C->T | Ts |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| TGFBP#04 | RGD | Yes, coding strand | Yes |
| At the mRNA level | On restriction map |
| NA | New restriction site(s): none Lost restriction site(s): PaeR7 I, Taq I, Xho I |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| BEL01GHE F0026 I2036 | Proband | Male | familial | 40 years old | BELGIUM |
| Phenotypic group | Disease |
| NA | Classical MFS |
| Symptom |
| CF-Dolichocephaly |
| CF-Down-slanting palpebral fissures |
| CF-Malar hypoplasia |
| O-Ectopia lentis |
| S-Arachnodactyly (M) |
| S-Chest deformity (unspecified) |
| S-Plain pes planus (M)(1) |
| S-Protusio acetabulæ (M)(2) |
| S-Scoliosis > 20° (M)(1) |
| Reference ID | PubMed ID | Reference |
| 89 | 11700157 | Loeys B, Nuytinck L, Delvaux I, De Bie S, De Paepe A. "Genotype and phenotype analysis of 171 patients referred for molecular study of the fibrillin-1 gene FBN1 because of suspected Marfan syndrome". Arch Intern Med. 2001 Nov 12;161(20):2447-54. |