| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.6993C>A | p.Cys2331X | Heterozygous | Mutation |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| TGC | Cys | TGA | Stop | C->A | Tv |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| cb EGF-like#36 | Disulfide bonds 2318-2331 (C6) | Yes, coding strand | No |
| At the mRNA level | On restriction map |
| NA | New restriction site(s): Mae III Lost restriction site(s): none |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| GER03HAN F0088 I0028 | Proband | NA | NA | GERMANY |
| Phenotypic group | Disease |
| NA | NA |
| Symptom |
| Clinical data will be implemented as soon as possible |
| Reference ID | PubMed ID | Reference |
| 182 | 19159394 | S*ylen B, Singh KK, Abuzainin A, Rommel K, Becker H, Arslan-Kirchner M, Schmidtke J. "Prevalence of dural ectasia in 63 gene-mutation-positive patients with features of Marfan syndrome type 1 and Loeys-Dietz syndrome and report of 22 novel FBN1 mutations". Clin Genet. 2009 Mar;75(3):265-70. |