Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
c.IVS1+36947G>A (c.31+36947G>A) | Hemizygous | Mutation |
wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
TAT | Tyr | spl+36947 | Spl. | G->A | Ts |
Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
At the mRNA level | On restriction map |
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 (%) | |||||
TTGGTTTTGCGGCTT |
| TTGGTTTTGCAGCTT |
| 33.1 % |
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 |
Normal size, medium quantity | Normal size, medium quantity |
Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
---138-0-1 | Proband | Male | Familial | 8 | FRANCE |
Phenotypic group |
BMD |
+ cardiomyopathy |
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. |