ClinVar Miner

Submissions for variant NM_000211.5(ITGB2):c.106T>G (p.Cys36Gly)

dbSNP: rs2084111337
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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 RCV001216150 SCV001387928 uncertain significance Leukocyte adhesion deficiency 1 2019-05-31 criteria provided, single submitter clinical testing 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. 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. This variant has not been reported in the literature in individuals with ITGB2-related conditions. This sequence change replaces cysteine with glycine at codon 36 of the ITGB2 protein (p.Cys36Gly). The cysteine residue is highly conserved and there is a large physicochemical difference between cysteine and glycine. This variant is not present in population databases (ExAC no frequency).

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