| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.1743G>T | p.Pro581Pro |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| CCG | Pro | CCT | Pro | G->T | Tv |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| 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) |
|---|---|---|
| 0.94 | 1.00 (non pathogenous) | 23 (Polymorphism) |
| Sample ID | Patient status |
| 20_20-52625262-02--- | Relative |
| Symptom |
| Reference ID | Reference |
| 20 | Unpublished data |