| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.5608A>T | p.Lys1870X | Heterozygous | Mutation |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| AAA | Lys | TAA | Stop | A->T | Tv |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| CRD-repeat #14 | Yes, non coding strand | No |
| At the mRNA level | On restriction map |
| presence of a second deleted RNA (exon 9 deletion) | 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 High | Irregular Medium | Irregular Medium | ||||
| Western Blot | ||
| dys 1 | dys 2 | dys 3 |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| ---851-0-2 | Proband | Female | Unknown |
| Phenotypic group |
| Symptomatic carrier |
| DMD carrier - Symptomatic |
| Reference ID | Reference |
| 1 | Unpublished data |