| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.8080C>T | p.Arg2694X | 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 |
| COOH unique region | Yes, coding strand | Yes |
| At the mRNA level | On restriction map |
| NA | New restriction site(s): Dde I Lost restriction site(s): BsaJ I, Hae III |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| AUS02WES F0017 I01 | Proband | NA | NA | ? (22 years old) | AUSTRALIA |
| Phenotypic group | Disease |
| NA | Classical MFS |
| Symptom |
| C-Asc. aortic dilatation |
| C-Mitral valve prolapse |
| L-Spontaneous pneumothorax |
| S-Arachnodactyly (M) |
| S-High arched palate |
| S-Joint hypermobility (m) |
| S-Pectus carinatum (M)(2) |
| SI-Significant striae atrophicae (m)(1) |
| Reference ID | PubMed ID | Reference |
| 114 | 14695540 | Biggin A, Holman K, Brett M, Bennetts B, Ades L. "Detection of thirty novel FBN1 mutations in patients with Marfan syndrome or a related fibrillinopathy". Hum Mutat. 2004 Jan;23(1):99. |