Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
c.32_650dup | p.Tyr11delinsTyrMet | Hemizygous | Mutation |
wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
TAT | Tyr | ins618b | InF | In frame ins |
Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
Dp427m unique N-Ter |
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 |
Increased size, medium quantity | Increased size, medium quantity |
Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
---607-0-1 | Proband | Male | Familial | FRANCE |
Phenotypic group |
DCM |
At skeletal muscle level, the patient had only hypertrophic calves, cramping but no muscle weakness. |
Reference ID | Reference |
1 | Unpublished data |