Submissions for variant NM_001384732.1(CPLANE1):c.3921+1G>A

Total submissions: 1

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	RCV005238287	SCV005885096	likely pathogenic	Joubert syndrome and related disorders	2024-12-18	criteria provided, single submitter	clinical testing	Variant summary: CPLANE1 c.3921+1G>A is located in a canonical splice-site and is predicted to affect mRNA splicing resulting in a significantly altered protein due to either exon skipping, shortening, or inclusion of intronic material. Variants that disrupt the consensus splice site are a relatively common cause of aberrant splicing and loss of CPLANE1 function. Several computational tools predict a significant impact on normal splicing: Four predict the variant abolishes a 5' splicing donor site. However, these predictions have yet to be confirmed by functional studies. The variant was absent in 246746 control chromosomes (gnomAD). c.3921+1G>A has been reported in the literature in at least one individual affected with Joubert Syndrome And Related Disorders (Liu_2020). To our knowledge, no experimental evidence demonstrating an impact on protein function has been reported. The following publications have been ascertained in the context of this evaluation (PMID: 32233090, 36789003, 34091942). No submitters have cited clinical-significance assessments for this variant to ClinVar. Based on the evidence outlined above, the variant was classified as likely pathogenic.