| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861365, TBCEL-TECTA
+1 more (E882K +1 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | TBCEL-TECTA, TECTA (S1963R +1 more) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 12 | |
| | TBCEL-TECTA, TECTA (T1866M +1 more) | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 21 +5 more | GConflicting classifications of pathogenicity |
| | TBCEL-TECTA, TECTA (R2021C +1 more) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 12 +1 more | GConflicting classifications of pathogenicity |
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