ClinVar Miner

Submissions for variant NM_024589.3(ROGDI):c.113T>G (p.Leu38Arg)

dbSNP: rs1555491894
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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 RCV000636833 SCV000758274 uncertain significance Amelocerebrohypohidrotic syndrome 2020-01-27 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. 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. This variant has not been reported in the literature in individuals with ROGDI-related disease. While this variant is not present in population databases, the frequency information is unreliable, as metrics indicate poor data quality at this position in the ExAC database. This sequence change replaces leucine with arginine at codon 38 of the ROGDI protein (p.Leu38Arg). The leucine residue is highly conserved and there is a moderate physicochemical difference between leucine and arginine.

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