ClinVar Miner

Submissions for variant NM_004522.3(KIF5C):c.2660A>G (p.Lys887Arg)

dbSNP: rs1210354255
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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 RCV001255797 SCV001432411 likely benign Complex cortical dysplasia with other brain malformations 2 no assertion criteria provided clinical testing

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