| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.138C>G | p.His46Gln |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| CAC | His | CAG | Gln | C->G | Tv |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Mismatch binding | 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) |
|---|---|---|
| 0.92 | 0.00 (pathogenous) | 71 (Probably pathogenous) |
| Sample ID | Patient status |
| 14_13C028913C0289 | Relative |
| Symptom |
| Reference ID | Reference |
| 14 | Unpublished data |