| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.1999C>T | p.Gln667X | Hemizygous | Mutation |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| CAG | Gln | TAG | Stop | C->T | Ts |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| CRD-repeat #3 | No | No |
| 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 | ||||
| Irregular Low | Irregular Low | |||||
| Western Blot | ||
| dys 1 | dys 2 | dys 3 |
| No signal | No signal |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| ---272-0-1 | Proband | Male | Familial | FRANCE |
| Phenotypic group |
| DMD |
| There is a maternal cousin carrying a splice site mutation in intron 22 (subject subject F3417610531 in this database) |
| Reference ID | Reference |
| 1 | Unpublished data |