| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.IVS1+2113del1delG (c.164+2113del1delG) | p.Met1? | Heterozygous | Polymorphism? |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| ATG | Met | spl+2113 | del1delG |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Signal peptide |
| At the mRNA level | On restriction map |
| Not tested on cDNA (needed) | New restriction site(s): none Lost restriction site(s): none |
| Impact on splicing | ||||||||||
| Splice site type | Wild type sequence | CV | Mutant type sequence | CV | Variation (%) | |||||
| GAAtgtatt |
| AATgtattg |
| 74.4 % | ||||||
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| FRA01BOU F0845 I0881 | Proband | Male | familial | FRANCE |
| Phenotypic group | Disease |
| NA | MFS |
| Symptom |
| Reference ID | PubMed ID | Reference |
| 207 | - | Boileau C. (personnal communication 2013) |