ClinVar Miner

Submissions for variant NM_021008.4(DEAF1):c.1544G>A (p.Cys515Tyr)

dbSNP: rs1057520182
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000426775 SCV000511649 uncertain significance not provided 2016-11-10 criteria provided, single submitter clinical testing Converted during submission to Uncertain significance.

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