ClinVar Miner

Submissions for variant NM_005422.4(TECTA):c.3854G>C (p.Cys1285Ser)

dbSNP: rs1060499597
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Division of Human Genetics, Children's Hospital of Philadelphia RCV000477960 SCV000536848 uncertain significance Autosomal dominant nonsyndromic hearing loss 12; Autosomal recessive nonsyndromic hearing loss 21 2015-11-13 no assertion criteria provided research

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