| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | TBCEL-TECTA, TECTA (S599T) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 12 | |
| | LOC126861365, TBCEL-TECTA
+1 more (N886S +1 more) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 12 +3 more | GConflicting classifications of pathogenicity |
| | TBCEL-TECTA, TECTA (S1847P) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 12 | |
Click to view in NCBI Gene