ClinVar Miner

Submissions for variant NM_000419.5(ITGA2B):c.2095-19T>A

dbSNP: rs2143447856
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ClinGen Platelet Disorders Variant Curation Expert Panel, ClinGen RCV002254790 SCV002525879 likely pathogenic Glanzmann thrombasthenia 2022-06-12 reviewed by expert panel curation The NM_000419.5(ITGA2B):c.2095-19T>A intronic variant is predicted to cause loss of the intron 20 canonical acceptor site by computational splicing predictor SpliceAI with a score of 0.98 for acceptor loss, it further predicts an acceptor site gain at c.2095-17, with a score of 1.00 (PP3). At least one patient (GT15 in PMID: 25728920) with this variant displayed mucocutaneous bleeding and impaired aggregation with all agonists except ristocetin, which is highly specific for Glanzmann thrombasthenia. Additionally, alphaIIb surface expression was absent, as measured by flow cytometry (PP4_strong). GT15 (PMID: 25728920) is compound heterozygous for Gln924Ter (classified Pathogenic by the PD-EP) and c.2095-19T>A (PM3_supporting). This variant is absent from gnomAD v2.1.1 (PM2_Supporting). In summary this variant meets criteria to be classified as Likely Pathogenic for autosomal recessive Glanzmann Thrombasthenia based on the ACMG/AMP criteria applied, as specified by the ClinGen PD VCEP: PP4_strong, PM2_supporting, PM3_supporting, PP3. (VCEP specifications version 2.1)

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