| Variation name (cDNA level) | Variation name (protein level) | Variation status |
| c.1261A>G | p.Ser421Gly |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| AGT | Ser | GGT | Gly | A->G | Ts |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| EXO1 interaction | 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) |
|---|---|---|
| 0.65 | 0.40 (non pathogenous) | 53 (Probable polymorphism) |
| Sample ID | Patient status |
| 20_20-3282_3282-01_13089 | Relative |
| Symptom |
| Reference ID | Reference |
| 20 | Unpublished data |