ClinVar Miner

Submissions for variant NM_181882.2(PRX):c.1837G>A (p.Val613Met) (rs773222045)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000200247 SCV000255224 uncertain significance Charcot-Marie-Tooth disease type 4 2015-01-07 criteria provided, single submitter clinical testing This sequence change replaces valine with methionine at codon 613 of the PRX protein (p.Val613Met). The valine residue is weakly conserved and there is a small physicochemical difference between valine and methionine. This sequence change has not been published in the literature and is not present in population databases. 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: "Deleterious"; PolyPhen-2: "possibly_damaging"; Align-GVGD: "Class C0"). In summary, this is a novel missense change with uncertain impact on protein function. It has been classified as a Variant of Uncertain Significance.

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