| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.7201_8391dup | p.Ser2798GlyfsX3 | Heterozygous | Mutation |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| AGG | Arg | ins1190a | Fs. | Stop at 2800 | Fr. |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| CRD-repeat #19 |
| At the mRNA level | On restriction map |
| New restriction site(s): none Lost restriction site(s): none |
| On isoforms (a blue cell indicates that the corresponding isoform is affected by the mutation) | ||||||
| Dp 427c | Dp 427m | Dp 427p | Dp 260 | Dp 140 | Dp 116 | Dp 71 |
| Immunofluorescence | ||||||
| dys 1 | dys 2 | dys 3 | ||||
| Mosaic Medium | ||||||
| Western Blot | ||
| dys 1 | dys 2 | dys 3 |
| Normal size, medium quantity | Normal size, medium quantity |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| ---951-0-2 | Proband | Female | De novo | FRANCE |
| Phenotypic group |
| Symptomatic carrier |
| + mental retardation (Autism). DMD carrier, symptomatic |
| Reference ID | Reference |
| 1 | Unpublished data |