ClinVar Miner

Submissions for variant NM_001963.6(EGF):c.2693G>A (p.Arg898Gln)

dbSNP: rs757524102
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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 RCV001968861 SCV002257474 uncertain significance not provided 2022-08-31 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 output the following: SIFT: "Not Available"; PolyPhen-2: "Benign"; Align-GVGD: "Not Available". The glutamine amino acid residue is found in multiple mammalian species, which suggests that this missense change does not adversely affect protein function. ClinVar contains an entry for this variant (Variation ID: 1468180). This variant has not been reported in the literature in individuals affected with EGF-related conditions. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the gnomAD database. This sequence change replaces arginine with glutamine at codon 898 of the EGF protein (p.Arg898Gln). The arginine residue is weakly conserved and there is a small physicochemical difference between arginine and glutamine.

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