Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
c.IVS8-15A>G (c.832-15A>G) | Hemizygous | Mutation |
wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
ATC | Ile | spl-15 | Spl. | A->G | Ts |
Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
CRD-hinge region #1 |
At the mRNA level | On restriction map |
r.831_832ins832-14_832-1 | 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 (%) | |||||
CCACTCCCCCAAACC |
| CCACTCCCCCAGACC |
| 33.3 % |
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 |
---151-9-11 | Relative | Male | Familial | FRANCE |
Phenotypic group |
DMD |
Reference ID | Reference |
106 | Unpublished data |