ClinVar Miner

Submissions for variant NM_004985.5(KRAS):c.221C>T (p.Thr74Ile)

dbSNP: rs1951405479
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Service de Génétique Moléculaire, Hôpital Robert Debré RCV001261057 SCV001438459 likely pathogenic Noonan syndrome no assertion criteria provided clinical testing

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