ClinVar Miner

Submissions for variant NM_002160.4(TNC):c.3295_3297delinsAAT (p.Gln1099Asn)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Prof. Karen Avraham, Tel Aviv University RCV004819276 SCV005439849 uncertain significance Autosomal dominant nonsyndromic hearing loss 56 2024-12-29 criteria provided, single submitter research The TNC c.3297-3299delCAGinsAAT:p.(Gln1099Asn) heterozygous variant is very rare and predicted deleterious. It was detected in an individual with sloping mild-to-severe HL.

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