ClinVar

Description

The c.7780dupT variant, located in coding exon 24 of the DSP gene, results from a duplication of T at nucleotide position 7780, causing a translational frameshift with a predicted alternate stop codon (p.S2594Ffs*31). Most frameshifts are typically deleterious in nature. This frameshift occurs at the 3' terminus of DSP and is not expected to trigger nonsense-mediated mRNA decay; however, the frameshift eliminates 278 amino acids in the C-terminus of the protein, which would be expected to impact both the intermediate filament and keratin interaction domains. A single nucleotide deletion at this position, c.7780delT, which also results in a translational frameshift and alternate stop codon (p.S2594Pfs*8), has been reported as homozygous in an individual with Carvajal syndrome; functional studies showed DSP expression in her carrier mother to be approximately 50% of wild-type levels (Rasmussen TB et al. Clin. Genet., 2013 Jul;84:20-30). Furthermore, alterations in DSP that result in haploinsufficiency or protein truncation, including some downstream of this variant, have been reported in patients with arrhythmogenic right ventricular cardiomyopathy (ARVC) and dilated cardiomyopathy (DCM) (Fressart V et al. Europace. 2010;12(6):861-8; Elliott P et al. Circ Cardiovasc Genet. 2010;3(4):314-22; Quarta G et al. Circulation. 2011;123(23):2701-9; Garcia-Pavia P et al. Heart. 2011;97(21):1744-52; Rasmussen TB et al. Clin Genet. 2013;84(1):20-30; Pugh TJ et al. Genet Med. 2014;16(8):601-8; Castelletti S et al. Int. J. Cardiol., 2017 Dec;249:268-273). Based on the majority of available evidence to date, this variant is likely to be pathogenic.