| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | TBCEL-TECTA, TECTA (C1285S +1 more) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 12 +1 more | |
| | TBCEL-TECTA, TECTA (R1462C +1 more) | Single nucleotide variant (missense variant) | not specified | |
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