ClinVar Miner

Submissions for variant NM_001378030.1(CCDC78):c.955_956delinsAA (p.Ala319Lys)

dbSNP: rs2040592043
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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 RCV001217799 SCV001389651 uncertain significance Congenital myopathy with internal nuclei and atypical cores 2019-06-05 criteria provided, single submitter clinical testing 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. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated, but these predictions have not been confirmed by published functional studies and their clinical significance is uncertain. This variant has not been reported in the literature in individuals with CCDC78-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces alanine with lysine at codon 319 of the CCDC78 protein (p.Ala319Lys). The alanine residue is moderately conserved and there is a moderate physicochemical difference between alanine and lysine.

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