The UMD-DMD France mutations database
Record ID: 667
Mutation description
| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.IVS70+1G>A (c.10223+1G>A) | Hemizygous | Mutation |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| ACT | Thr | spl+1 | Spl. | G->A | Ts |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
Mutation impact
| At the mRNA level | On restriction map |
| r.10087_10233del | 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 (%) | |||||
| AACgtgagt |
| AACatgagt |
| -30.9 % | ||||||
| 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 |
Patient and sample data
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| ---424-0-1 | Proband | Male | Familial | 3 |
| Phenotypic group |
| DMD |
Associated pictures
 DYS I |
 DYS II |
 Myosin |
Comments
| + Mental retardation |
Reference
| Reference ID | PubMed ID | Reference |
| 10 | 17041906 | Deburgrave N, Daoud F, Llense S, Barbot JC, R*can D, Peccate C, Burghes AH, B*roud C, Garcia L, Kaplan JC, Chelly J, Leturcq F. Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene. Hum Mutat. 2007 Feb;28(2):183-95. |