The UMD-THAP1 mutations database
Record ID: 65

Mutation description

Variation name (cDNA level)	Variation name (protein level)	Variation status	Variation class
c.241T>C	p.Phe81Leu	Heterozygous	Mutation

wt codon	wt aa	mutant codon	mutant aa	mutational event	mutation type
TTT	Phe	CTT	Leu	T->C	Ts

Structure	Key Residue (HCD)	Pyrimidin doublet	CpG
H4-THAP dom.	AA interactions	Yes, coding strand	No

Mutation impact

At the mRNA level	On restriction map
NA	New restriction site(s): none Lost restriction site(s): Ssp I

Conservation (0-1)	SIFT (0-1)	UMD-predictor (0-100)
0.79	0.45 (non pathogenous)	59 (Probable polymorphism)

Patient and sample data

Sample ID	Patient ID	Family ID	Patient status	Gender	Transmission	Geographic origin
USA01NYO F0001 I0002	413	family S	Relative	Male	Familial	GERMANY

Phenotypic group	Disease
NA	Generalized dystonia

Associated pictures

Genealogic tree

Clinical data

Symptom	Age
Age at last examination	46
Arm	46
Cranial	46
Face	46
Jaw	46
Leg	13
Neck	46
Tongue	46
Trunk	46

Reference

Reference ID	PubMed ID	Reference
1	19182804	Fuchs T, Gavarini S, Saunders-Pullman R, Raymond D, Ehrlich ME, Bressman SB, Ozelius LJ. Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia. Nat Genet. 2009 Mar;41(3):286-8.