| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class | 
| c.6439_6614del | p.Glu2147AlafsX17 | Hemizygous | Mutation | 
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type | 
| GAA | Glu | del176a | Fs. | Stop at 2163 | Fr. | 
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG | 
| CRD-repeat #17 | 
| 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 | 
| No signal with Revertant fibers | No signal with Revertant fibers | No signal with Revertant fibers | 
| Western Blot | ||
| dys 1 | dys 2 | dys 3 | 
| No signal | 
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin | 
| ---035-1-71 | Proband | Male | Unknown | FRANCE | 
| Phenotypic group | 
| DMD | 
| WB Dys1 : very low expression (size?) | 
| Reference ID | Reference | 
| 115 | Unpublished data |