ClinVar

Description

Variant summary: VCL c.625A>T (p.Met209Leu) results in a conservative amino acid change in the encoded protein sequence. Four of five in-silico tools predict a benign effect of the variant on protein function. The variant allele was found at a frequency of 3.6e-05 in 249842 control chromosomes. The available data on variant occurrences in the general population are insufficient to allow any conclusion about variant significance. c.625A>T has been reported in the literature in individuals affected with Dilated Cardiomyopathy, without strong evidence for causality (Zhao_2015, Shen_2022). These reports do not provide unequivocal conclusions about association of the variant with Cardiomyopathy. At least one publication reports experimental evidence evaluating an impact on protein function in relation to neural tube defects. These results showed no alteration in protein levels compared to wild-type, no effects on both basic and Wnt5A-activated PCP signaling as well as no distinct change in cell migration (Wang_2021). However, the impact of these outcomes on cardiomyopathy is unclear. Three clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar after 2014 without evidence for independent evaluation. All laboratories classified the variant as uncertain significance. Based on the evidence outlined above, the variant was classified as uncertain significance.