| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.6857C>T | p.Ala2286Val |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GCC | Ala | GTC | Val | C->T | Ts |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Microtubule binding domain (ba | Yes, 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) |
|---|---|---|
| 0.62 | 0.14 (non pathogenous) | 41 (Polymorphism) |
| Sample ID | Patient status |
| 37_P13.29-E20953146399 | Relative |
| Symptom |
| Reference ID | Reference |
| 37 | Unpublished data |