ClinVar Miner

Submissions for variant NM_001972.4(ELANE):c.676G>A (p.Gly226Arg)

dbSNP: rs780046041
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001937506 SCV002129193 uncertain significance Cyclical neutropenia; Neutropenia, severe congenital, 1, autosomal dominant 2020-12-13 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 been observed in individual(s) with severe congenital neutropenia (PMID: 25427142). This variant is present in population databases (rs780046041, ExAC 0.002%). This sequence change replaces glycine with arginine at codon 226 of the ELANE protein (p.Gly226Arg). The glycine residue is highly conserved and there is a moderate physicochemical difference between glycine and arginine.
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002264407 SCV002543429 uncertain significance Autoinflammatory syndrome 2018-12-01 criteria provided, single submitter clinical testing

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