ClinVar Miner

Submissions for variant NM_001005361.3(DNM2):c.695T>G (p.Ile232Ser)

dbSNP: rs749672066
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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 RCV001369344 SCV001565780 uncertain significance Charcot-Marie-Tooth disease dominant intermediate B 2020-03-15 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals with DNM2-related conditions. 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 disruptive, but 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. This variant is not present in population databases (ExAC no frequency). This sequence change replaces isoleucine with serine at codon 232 of the DNM2 protein (p.Ile232Ser). The isoleucine residue is highly conserved and there is a large physicochemical difference between isoleucine and serine.

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