| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.IVS60-15519G>T (c.9085-15519G>T) | Hemizygous | Mutation |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GTG | Val | spl-15519 | Spl. | G->T | Tv |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| At the mRNA level | On restriction map |
| r.[9084_9085ins9085-15609_9085-15521, =] | 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 (%) | |||||
| AAGggaagc |
| AAGgtaagc |
| 27.7 % | ||||||
| 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 | ||||
| Western Blot | ||
| dys 1 | dys 2 | dys 3 |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| ---160-1-1 | Relative | Male | Familial | FRANCE |
| Phenotypic group |
| DMD |
| + Mental retardation. Case 1 in the report (patient BB). |
| Reference ID | PubMed ID | Reference |
| 4 | 14659407 | Beroud C, Carrie A, Beldjord C, Deburgrave N, Llense S, Carelle N, Peccate C, Cuisset JM, Pandit F, Carre-Pigeon F, Mayer M, Bellance R, Recan D, Chelly J, Kaplan JC, Leturcq F."Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene."Neuromuscul Disord. 2004 Jan;14(1):10-8. |