The variant NM_001100.4:c.1043T>A in ACTA1 is a missense variant predicted to cause substitution of leucine by glutamine at amino acid 348 (p.Leu348Gln). The variant is absent from gnomAD v4.1.0 with adequate coverage (PM2_Supporting). The REVEL computational prediction analysis tool gives a score of 0.976, which is above the threshold necessary to apply PP3. In addition, ACTA1, in which the variant was identified, is defined by the ClinGen Congenital Myopathies VCEP as a gene that has a low rate of benign missense variation and where pathogenic missense variants are a common mechanism of disease (PP2). This variant has been reported in two probands with congenital myopathy (PS4_Supporting, PMID:25747004, SCV002280810.3). The one proband had hypotonia at birth, end stage limb-girdle dystrophy with diffuse proximal and distal weakness and wasting, and weak axial muscles. Muscle biopsy of this proband showed nemaline rods and electron microscopy showed few zebra bodies and accumulation of actin-like thin filaments (PP4_Moderate, PMID:25747004). In summary, the variant meets the criteria to be classified as likely pathogenic for autosomal dominant alpha-actinopathy. ACMG/AMP criteria met, as specified by the ClinGen Congenital Myopathies VCEP: PP4_Moderate, PS4_Supporting, PP2, PP3, PM2_Supporting (ClinGen Congenital Myopathies VCEP specifications version 2; 08/27/2024).