ClinVar

Description

Variant summary: The variant involves the deletion of exon 11 in the CDK13 gene. A presumed nomenclature of c.(2897+1_2898-1)_(3029+1_3030-1)del has been designated for the purposes of this classification. This Copy Number Variant (CNV) is predicted to result in an in-frame deletion within this gene. The variant was absent in 21694 control chromosomes. The available data on variant occurrences in the general population are insufficient to allow any conclusion about variant significance. To our knowledge, no occurrence of c.(2897+1_2898-1)_(3029+1_3030-1)del in individuals affected with Congenital Heart Defects, Dysmorphic Facial Features, And Intellectual Developmental Disorder and no experimental evidence demonstrating its impact on protein function have been reported. No submitters have cited clinical-significance assessments for this variant to ClinVar. Based on the evidence outlined above, the variant was classified as uncertain significance.