ClinVar Miner

Submissions for variant NM_003036.4(SKI):c.1354C>A (p.Pro452Thr)

dbSNP: rs1417738788
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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 RCV001346655 SCV001540877 uncertain significance Shprintzen-Goldberg syndrome 2020-09-02 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. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt SKI protein function. This variant has not been reported in the literature in individuals with SKI-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces proline with threonine at codon 452 of the SKI protein (p.Pro452Thr). The proline residue is highly conserved and there is a small physicochemical difference between proline and threonine.

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