| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.4706A>G | p.Asp1569Gly |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GAT | Asp | GGT | Gly | A->G | Ts |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Axin binding domain 1 | 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) |
|---|---|---|
| 0.75 | 0.05 (pathogenous) | 79 (Pathogenous) |
| Sample ID | Patient status |
| 33_PSL416---08-1909 | Relative |
| Symptom |
| Reference ID | Reference |
| 33 | Unpublished data |