Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
c.8668G>A | p.Glu2890Lys | Hemizygous | Mutation |
wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
GAG | Glu | AAG | Lys | G->A | Ts |
Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
CRD-repeat #23 | Yes, non coding strand | No |
At the mRNA level | On restriction map |
2RNAs: del 58 + del58-59 | New restriction site(s): none Lost restriction site(s): none |
Pathogenicity (bioinformatics predictions) | ||
Conservation (0-1) | SIFT (0-1) | UMD predictor (0-100) |
0 | - | 88 (Pathogenous) |
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 |
---100-4-11 | Proband | Male | Unknown | FRANCE |
Phenotypic group |
DMD |
+ Mental retardation. |
Reference ID | Reference |
1 | Unpublished data |