| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.7868A>C | p.His2623Pro | Heterozygous | Mutation |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| CAC | His | CCC | Pro | A->C | Tv |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| cb EGF-like #42 | Ca2+ binding | No | No |
| At the mRNA level | On restriction map |
| NA | New restriction site(s): BstX I Lost restriction site(s): Mae III |
| Conservation (0-1) | SIFT (0-1) | UMD-predictor (0-100) |
|---|---|---|
| 1 | 0.07 (non pathogenous) | 100 (Pathogenous) |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| USA05HOU F0003 I01 | Proband | NA | de novo | ? (30 years old) | U.S.A |
| Phenotypic group | Disease |
| NA | Classical MFS |
| Symptom |
| C-Asc. aortic dilatation |
| O-Ectopia lentis |
| O-Myopia |
| S-Arachnodactyly (M) |
| S-Arm span/height >1.05 (M) |
| S-Chest deformity (unspecified) |
| S-Dolichostenomelia |
| S-Long bone over growth |
| S-Plain pes planus (M)(1) |
| S-Reduced US/LS ratio <0.87 (M) |
| S-Scoliosis > 20° (M)(1) |
| SI-Other herniae |
| Reference ID | PubMed ID | Reference |
| 24 | - | Grossfield J, Cao S; Milewicz DM. "Characterization of mutations involving the carboxy-terminal domain of fibrillin-1 indicates a role of this domain in secretion in dermal fibroblasts". Am J Hum Genet 1993, 53 abstract 1167 . |