Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
c.3350G>A | p.Cys1117Tyr | Heterozygous | Mutation |
wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
TGT | Cys | TAT | Tyr | G->A | Ts |
Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
cb EGF-like #13 | Disulfide bonds 1117-1129 (C1) | No | No |
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) |
---|---|---|
0.83 | 0.00 (pathogenous) | 100 (Pathogenous) |
Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
AUS01NAD F0007 I01 | Proband | NA | de novo | ? (10 years old) | AUSTRALIA |
Phenotypic group | Disease |
NA | Infantil MFS |
Symptom |
C-Asc. aortic dilatation |
C-Mitral regurgitation |
C-Mitral valve prolapse |
CF-Blue sclerae |
O-Adhesion of iris with cornea |
O-Congenital miosis |
O-Ectopia lentis |
O-Iridodonesis |
S-Characteristic facial appearance |
S-Dolichostenomelia |
S-Joint hypermobility (m) |
S-Pectus excavatum moderate (m)(1) |
S-Plain pes planus (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. |