The UMD-THAP1 mutations database
Record ID: 30

Mutation description

Variation name (cDNA level)	Variation name (protein level)	Variation status	Variation class
c.25G>T	p.Gly9Cys	Heterozygous	Mutation

wt codon	wt aa	mutant codon	mutant aa	mutational event	mutation type
GGC	Gly	TGC	Cys	G->T	Tv

Structure	Key Residue (HCD)	Pyrimidin doublet	CpG
L1-THAP dom.		Yes, non coding strand	No

Mutation impact

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

Conservation (0-1)	SIFT (0-1)	UMD-predictor (0-100)
0.71	0.02 (pathogenous)	93 (Pathogenous)

Patient and sample data

Sample ID	Patient ID	Family ID	Patient status	Gender	Transmission	Geographic origin
USA02MEN F0001 I0001	A-1339 (II-2)		Proband	Female	Familial	U.S.A.

Phenotypic group	Disease
NA	Multifocal dystonia

Associated pictures

Genealogic tree

Clinical data

Symptom	Severity	Age
Age at last examination		60
Age of onset	hand	8
Arm		8
Jaw		35
Neck		35

Reference

Reference ID	PubMed ID	Reference
7	20083799	Xiao J, Zhao Y, Bastian RW, Perlmutter JS, Racette BA, Tabbal SD, Karimi M, Paniello RC, Wszolek ZK, Uitti RJ, Van Gerpen JA, Simon DK, Tarsy D, Hedera P, Truong DD, Frei KP, Dev Batish S, Blitzer A, Pfeiffer RF, Gong S, LeDoux MS. Novel THAP1 sequence variants in primary dystonia. Neurology. 2010 Jan 19;74(3):229-38.