| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.662A>G | p.Asp221Gly | Heterozygous | Mutation |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GAC | Asp | GGC | Gly | A->G | Ts |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| Ligand Binding 5 | Ligand Binding 5 | Yes, non coding strand |
| At the mRNA level | On restriction map |
| New restriction site(s): Bcn I, BsaJ I, Hpa II, Msp I, Nci I Lost restriction site(s): none |
| Pathogenicity (bioinformatics predictions) | ||
| Conservation (0-1) | SIFT (0-1) | UMD predictor (0-100) |
| 0 | - | 94 (Pathogenous) |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| D200G | Proband | NETHERLAND |
| Phenotypic group | Disease |
| Heterozygote |
| Reference ID | Reference |
| 167 | Unpublished data |