ClinVar Miner

Submissions for variant NM_005267.5(GJA8):c.566C>T (p.Pro189Leu)

dbSNP: rs397515627
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dept. Genetics and Cancer, Menzies Institute for Medical Research, University of Tasmania RCV000059334 SCV005081757 uncertain significance Cataract 1 multiple types 2023-01-21 criteria provided, single submitter curation Variant identified and curated during a GJA8 specific review of the literature in relation to pediatric or congenital cataract. ACMG-AMP criteria applied: PM2(Supporting), PP3. Original variant report: PMID:17724170. Gene review and curation guidelines are outlined in: https://doi.org/10.1080/17469899.2023.2160320
OMIM RCV000059334 SCV000105912 pathogenic Cataract 1 multiple types 2007-09-01 no assertion criteria provided literature only

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