The UMD-DMD France mutations database
Record ID: 588
Mutation description
| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.6439_7098del | p.Glu2147_Gln2366del | Hemizygous | Mutation |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GAA | Glu | del660a | InF | In frame del | InF |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| CRD-repeat #17 |
Mutation impact
| 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 Medium | Irregular Medium | Irregular Medium | ||||
| Western Blot | ||
| dys 1 | dys 2 | dys 3 |
| Reduced size, medium quantity (220 kDa) | Reduced size, medium quantity (220 kDa) |
Patient and sample data
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| ---161-0-1 | Proband | Male | Familial | 10 | FRANCE |
| Phenotypic group |
| BMD |
Associated pictures
 DYS I |
 Myosin |
Comments
| + Epilepsia |
Reference
| Reference ID | Reference |
| 1 | Unpublished data |