Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
c.4206T>G | p.Cys1402Trp | Heterozygous | Mutation |
wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
TGT | Cys | TGG | Trp | T->G | Tv |
Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
cb EGF-like #19 | Disulfide bonds 1391-1402 (C6) | No | No |
At the mRNA level | On restriction map |
NA | New restriction site(s): none Lost restriction site(s): Csp6 I, Rsa I |
Conservation (0-1) | SIFT (0-1) | UMD-predictor (0-100) |
---|---|---|
1 | 0.00 (pathogenous) | 100 (Pathogenous) |
Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
USA03STA F0058 I23 | Proband | NA | NA | ? (26 years old) | U.S.A |
Phenotypic group | Disease |
Type IV | Classical MFS |
Symptom | Severity |
C-Aortic surgery | |
C-Asc. aortic dilatation | |
C-Asc. aortic dissection | |
C-Mitral regurgitation | |
O-Ectopia lentis | |
O-Myopia | |
O-Retinal detachment | |
S-Arachnodactyly (M) | |
S-Crowding teeth (m) | |
S-Dolichostenomelia | |
S-High arched palate | |
S-Joint hypermobility (m) | |
S-Pectus carinatum (M)(2) | |
S-Scoliosis > 20° (M)(1) | mild |
SI-Significant striae atrophicae (m)(1) |
Reference ID | PubMed ID | Reference |
57 | 10486319 | Schrijver I, Liu W, Brenn T, Furthmayr H, Francke U. "Cysteine Substitutions in Epidermal Growth Factor-Like Domains of Fibrillin-1: Distinct Effects on Biochemical and Clinical Phenotypes". Am J Hum Genet 1999 Oct;65(4):1007-1020. |