| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.2136dup | p.Ser713GlnfsX11 | Heterozygous | Mutation |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| AGT | Ser | ins1a | Fs. | Stop at 723 | Fr. |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| TGFBP#02 | No |
| At the mRNA level | On restriction map |
| Duplication flanked by direct repeats | New restriction site(s): BspW I, BstK I, Dsa V, ScrF I Lost restriction site(s): BsaJ I, BstN I, EcoR II, Hae III, Pst I |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| GER05DOR F0009 I0001 | Proband | NA | NA | GERMANY |
| Phenotypic group | Disease |
| NA | NA |
| Symptom |
| Reference ID | PubMed ID | Reference |
| 147 | 17418587 | Waldmuller S, Muller M, Warnecke H, Rees W, Schols W, Walterbusch G, Ennker J, Scheffold T. "Genetic testing in patients with aortic aneurysms/dissections: a novel genotype/phenotype correlation?" Eur J Cardiothorac Surg. 2007 Jun;31(6):970-5. |