ClinVar Miner

Submissions for variant NM_018718.3(CEP41):c.383A>G (p.Asn128Ser)

dbSNP: rs782436531
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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 RCV000809209 SCV000949352 uncertain significance Joubert syndrome 15 2018-08-09 criteria provided, single submitter clinical testing This sequence change replaces asparagine with serine at codon 128 of the CEP41 protein (p.Asn128Ser). The asparagine residue is moderately conserved and there is a small physicochemical difference between asparagine and serine. This variant is present in population databases (rs782436531, ExAC 0.006%). This variant has not been reported in the literature in individuals with CEP41-related disease. Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Tolerated"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0". The serine amino acid residue is found in multiple mammalian species, suggesting that this missense change does not adversely affect protein function. These predictions have not been confirmed by published functional studies and their clinical significance is uncertain. 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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