| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.805A>G | p.Met269Val |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| ATG | Met | GTG | Val | A->G | Ts |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| HhH & pseudo-HhH | No | 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) |
|---|---|---|
| 1 | 0.00 (pathogenous) | 47 (Polymorphism) |
| Sample ID | Patient status |
| 37_P00.0123086142380 | Relative |
| Symptom |
| Reference ID | Reference |
| 37 | Unpublished data |