| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.64delA | p.Ser22AlafsX13 | Heterozygous | Mutation |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| AGC | Ser | del1a | Fs. | Stop at 34 | Fr. |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Signal peptide |
| At the mRNA level | On restriction map |
| No mechanism suspected | New restriction site(s): none Lost restriction site(s): none |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| CHI01HKO F0003 I0001 | Proband | NA | NA | CHINA |
| Phenotypic group | Disease |
| NA | NA |
| Symptom |
| Clinical data will be implemented as soon as possible |
| Reference ID | PubMed ID | Reference |
| 181 | 19533785 | Chung BH, Lam ST, Tong TM, Li SY, Lun KS, Chan DH, Fok SF, Or JS, Smith DK, Yang W, Lau YL. "Identification of novel FBN1 and TGFBR2 mutations in 65 probands with Marfan syndrome or Marfan-like phenotypes". Am J Med Genet A. 2009 Jul;149A(7):1452-9. |