ClinVar Miner

Submissions for variant NM_003921.5(BCL10):c.433G>C (p.Glu145Gln)

dbSNP: rs2100743637
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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 RCV001995452 SCV002267212 uncertain significance Immunodeficiency 37 2021-09-19 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals affected with BCL10-related conditions. 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 tolerated. This variant is not present in population databases (ExAC no frequency). This sequence change replaces glutamic acid with glutamine at codon 145 of the BCL10 protein (p.Glu145Gln). The glutamic acid residue is moderately conserved and there is a small physicochemical difference between glutamic acid and glutamine.

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