| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.1145G>A | p.Gly382Asp |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GGT | Gly | GAT | Asp | G->A | 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 |
| Conservation (0-1) | SIFT (0-1) | UMD-predictor (0-100) |
|---|---|---|
| 0.93 | 0.49 (non pathogenous) | 76 (Pathogenous) |
| Sample ID | Patient status |
| 33_SAT12306-1222--- | Relative |
| Symptom |
| Reference ID | Reference |
| 33 | Unpublished data |