| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.[2143G>T; 2144G>A; 2145A>G] | p.Gly715X | Heterozygous | Mutation |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GGA | Gly | TAG | Stop | G->T/G->A/A->G | Tv/Ts/Ts |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Yes, non coding strand | No |
| At the mRNA level | On restriction map |
| New restriction site(s): none Lost restriction site(s): none |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| 08STR1 | Proband | FRANCE |
| Phenotypic group | Disease |
| Symptom |
| Reference ID | Reference |
| 0 | Unpublished data |