Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
c.1633C>T | p.Arg545Cys | Heterozygous | Mutation |
wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
CGC | Arg | TGC | Cys | C->T | Ts |
Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
cb EGF-like #04 | No | Yes |
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) |
---|---|---|
0.67 | 0.00 (pathogenous) | 94 (Pathogenous) |
Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
UKD05LON F0017 I01 | Proband | Male | familial | U.K. |
Phenotypic group | Disease |
NA | Classical MFS |
Symptom |
C-Asc. aortic dilatation |
O-Ectopia lentis |
S-High arched palate |
S-Joint hypermobility (m) |
S-Pectus excavatum moderate (m)(1) |
SI-Significant striae atrophicae (m)(1) |
Reference ID | PubMed ID | Reference |
108 | 12446365 | Comeglio P, Evans AL, Brice G, Cooling RJ, Child AH. "Identification of FBN1 gene mutations in patients with ectopia lentis and marfanoid habitus". Br J Ophthalmol. 2002 Dec;86(12):1359-62. |