| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.6414delA | p.Lys2138AsnfsX22 | Heterozygous | Mutation |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| AAA | Lys | del1c | Fs. | Stop at 2159 | Fr. |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| cb EGF-like #32 |
| At the mRNA level | On restriction map |
| Deletion in a stretch of nucleotides | New restriction site(s): none Lost restriction site(s): none |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| BEL01GHE F0199 I0001 | Proband | NA | NA | BELGIUM |
| Phenotypic group | Disease |
| NA | MFS |
| Symptom |
| Reference ID | PubMed ID | Reference |
| 225 | 21542060 | Baetens M, Van Laer L, De Leeneer K, Hellemans J, De Schrijver J, Van De Voorde H, Renard M, Dietz H, Lacro RV, Menten B, Van Criekinge W, De Backer J, De Paepe A, Loeys B, Coucke PJ. "Applying massive parallel sequencing to molecular diagnosis of Marfan and Loeys-Dietz syndromes". Hum Mutat. 2011 Sep;32(9):1053-62. |