ClinVar Miner

Submissions for variant NM_147127.5(EVC2):c.431C>T (p.Ser144Phe)

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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 RCV003801853 SCV004597184 uncertain significance Ellis-van Creveld syndrome; Curry-Hall syndrome 2023-06-21 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals affected with EVC2-related conditions. 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. An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant is likely to be disruptive. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces serine, which is neutral and polar, with phenylalanine, which is neutral and non-polar, at codon 144 of the EVC2 protein (p.Ser144Phe).

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