ClinVar Miner

Submissions for variant NM_024577.3(SH3TC2):c.4G>A (p.Gly2Ser) (rs1554124107)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000654087 SCV000775977 uncertain significance Charcot-Marie-Tooth disease type 4 2017-09-06 criteria provided, single submitter clinical testing This sequence change replaces glycine with serine at codon 2 of the SH3TC2 protein (p.Gly2Ser). The glycine residue is moderately conserved and there is a small physicochemical difference between glycine and serine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with SH3TC2-related disease. Algorithms developed to predict the effect of missense changes on protein structure and function do not agree on the potential impact of this missense change (SIFT: "Tolerated"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). 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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