| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.756G>T | p.Gln252His |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| CAG | Gln | CAT | His | G->T | Tv |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Connector | 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) |
|---|---|---|
| 0.38 | 0.08 (non pathogenous) | 53 (Probable polymorphism) |
| Sample ID | Patient status |
| SO_-3200---G03554 | Relative |
| Symptom |
| Reference ID | Reference |
| 71 | Unpublished data |