ClinVar

Description

This missense variant replaces leucine with methionine at codon 10 of the ACTC1 protein. Computational prediction suggests that this variant may have a deleterious impact on protein structure and function (internally defined REVEL score threshold >= 0.7, PMID: 27666373). To our knowledge, functional studies have not been reported for this variant. This variant has been reported in individuals affected with hypertrophic cardiomyopathy (PMID: 22555271, 23054336, 27532257, 28138913, 35026164; communication with an external laboratory; ClinVar SCV000676951.5). In one case, this variant was reported in an individual affected with hypertrophic cardiomyopathy and poor clinical course who also carried a pathogenic splice variant in the MYBPC3 gene (PMID: 28138913). This variant has also been reported in a young individual affected with ventricular fibrillation and cardiac arrest (PMID: 31246743). This variant has been identified in 9/282084 chromosomes in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance.