| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.197_198delAG | p.Glu66ValfsX19 | Heterozygous | Mutation |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| GAG | Glu | del2b | Fs. | Stop at 84 | Fr. |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| L4-THAP dom. |
| At the mRNA level | On restriction map |
| Deletion of a repeated sequence | New restriction site(s): none Lost restriction site(s): none |
| Sample ID | Patient ID | Family ID | Patient status | Gender | Transmission | Geographic origin |
| GER02TUE F0008 I0001 | Case 8 | - | Proband | Female | Unknown | GERMANY |
| Phenotypic group | Disease |
| NA | Asymptomatic control |
| Symptom |
| Asymptomatic |
| Reference ID | PubMed ID | Reference |
| 12 | 20669277 | S*hn AS, Gl*ckle N, Doetzer AD, Deuschl G, Felbor U, Topka HR, Sch*ls L, Riess O, Bauer P, MŸller U, Grundmann K. Prevalence of THAP1 sequence variants in German patients with primary dystonia. Mov Disord. 2010 Sep 15;25(12):1982-6. |