ClinVar Miner

Submissions for variant NM_014053.4(FLVCR1):c.169C>G (p.Leu57Val)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001234443 SCV001407090 uncertain significance not provided 2020-08-25 criteria provided, single submitter clinical testing This sequence change replaces leucine with valine at codon 57 of the FLVCR1 protein (p.Leu57Val). The leucine residue is weakly conserved and there is a small physicochemical difference between leucine and valine. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate insufficient coverage at this position in the ExAC database. This variant has not been reported in the literature in individuals with FLVCR1-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 tolerated, 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.
Athena Diagnostics Inc RCV001234443 SCV001475857 uncertain significance not provided 2020-09-02 criteria provided, single submitter clinical testing

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