ClinVar Miner

Submissions for variant NM_003793.4(CTSF):c.593_594del (p.Thr197_Tyr198insTer)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004766668 SCV005381648 pathogenic Neuronal ceroid lipofuscinosis 2024-08-01 criteria provided, single submitter clinical testing Variant summary: CTSF c.593_594delAT (p.Tyr198X) results in a premature termination codon, predicted to cause a truncation of the encoded protein or absence of the protein due to nonsense mediated decay, which are commonly known mechanisms for disease. The variant was absent in 251482 control chromosomes. To our knowledge, no occurrence of c.593_594delAT in individuals affected with Neuronal Ceroid-Lipofuscinosis (Batten Disease) has 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 pathogenic.

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