ClinVar Miner

Submissions for variant NM_033360.4(KRAS):c.57G>T (p.Leu19Phe)

dbSNP: rs121913538
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000433336 SCV000504835 likely pathogenic Angiosarcoma 2015-07-14 no assertion criteria provided literature only
Department of Pathology and Laboratory Medicine, Sinai Health System RCV001354208 SCV001548761 likely pathogenic not provided no assertion criteria provided clinical testing

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