ClinVar Miner

Submissions for variant NM_003921.5(BCL10):c.370C>G (p.Pro124Ala)

dbSNP: rs1250409831
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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 RCV000798118 SCV000937717 uncertain significance Immunodeficiency 37 2018-12-25 criteria provided, single submitter clinical testing This sequence change replaces proline with alanine at codon 124 of the BCL10 protein (p.Pro124Ala). The proline residue is moderately conserved and there is a small physicochemical difference between proline and alanine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with BCL10-related conditions. 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, 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.

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