ClinVar Miner

Submissions for variant NM_001378030.1(CCDC78):c.898_900del (p.His300del)

dbSNP: rs771582682
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000706133 SCV000835165 uncertain significance Congenital myopathy with internal nuclei and atypical cores 2018-03-22 criteria provided, single submitter clinical testing This variant, c.898_900delCAC, results in the deletion of 1 amino acid of the CCDC78 protein (p.His300del), but otherwise preserves the integrity of the reading frame. This variant is present in population databases (rs771582682, ExAC 0.02%). This variant has not been reported in the literature in individuals with CCDC78-related disease. Experimental studies and prediction algorithms are not available for this variant, and the functional significance of the deleted amino acid is currently unknown. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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