ClinVar Miner

Submissions for variant NM_001368809.2(AMPD2):c.1871G>T (p.Gly624Val)

gnomAD frequency: 0.00004  dbSNP: rs1349754803
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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 RCV001248441 SCV001421928 uncertain significance Hereditary spastic paraplegia 63; Pontocerebellar hypoplasia type 9 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 are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals with AMPD2-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces glycine with valine at codon 678 of the AMPD2 protein (p.Gly678Val). The glycine residue is highly conserved and there is a moderate physicochemical difference between glycine and valine.

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