ClinVar

Description

Based on the classification scheme VCGS_Germline_v1.3.4, this variant is classified as Likely pathogenic. Following criteria are met: 0103 - Dominant negative and gain of function are known mechanisms of disease in this gene and are associated with arrhythmogenic right ventricular dysplasia 2 (MIM#600996) and ventricular tachycardia, catecholaminergic polymorphic, 1 (CPVT) (MIM#604772) (PMID: 12459180, 27646203, 29477366). (I) 0107 - This gene is associated with autosomal dominant disease. (I) 0112 - The condition associated with this gene has incomplete penetrance (OMIM). (I) 0200 - Variant is predicted to result in a missense amino acid change from threonine to isoleucine. (I) 0251 - This variant is heterozygous. (I) 0301 - Variant is absent from gnomAD (both v2 and v3). (SP) 0309 - An alternative amino acid change at the same position has been observed in gnomAD (v2) (34 heterozygotes, 0 homozygotes). (I) 0502 - Missense variant with conflicting in silico predictions and uninformative conservation. (I) 0602 - Variant is located in a hotspot region or cluster of pathogenic variants. This variant is located in the N-terminal domain, one of the known hot spot regions (PMID: 19926015). (SP) 0703 - Other missense variants comparable to the one identified in this case have moderate previous evidence for pathogenicity. An alternative variant in the same codon, p.(Thr415Lys), has been reported as likely pathogenic in ClinVar. Another variant in the same codon, p.(Thr415Arg), has been reported as pathogenic in patients with catecholaminergic polymorphic ventricular tachycardia (CPVT) (Global Variome shared LOVD, PMID: 19926015, PMID: 27452199). (SP) 0808 - Previous reports of pathogenicity for this variant are conflicting. This variant has been previously reported in a family with CPVT, however the number of family members tested was not reported (PMID: 28789916). This variant has also been reported as a positive control sample for CPVT in a study comparing sequencing methods for inherited arrhythmia conditions, however no clinical details were provided for this sample (PMID: 22956155). Additionally, this variant has been classified as a VUS in a literature review (PMID: 32152366). (I) 0905 - No published segregation evidence has been identified for this variant. (I) 1007 - No published functional evidence has been identified for this variant. (I) 1208 - Inheritance information for this variant is not currently available in this individual. (I) Legend: (SP) - Supporting pathogenic, (I) - Information, (SB) - Supporting benign