ClinVar Miner

Submissions for variant NM_001029883.3(PCARE):c.2822G>A (p.Trp941Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
INSERM U1051, Institut des Neurosciences de Montpellier RCV001249866 SCV001424141 likely pathogenic Retinitis pigmentosa 2020-06-24 criteria provided, single submitter research

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