| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | TBCEL-TECTA, TECTA (S373fs +1 more) | Duplication (frameshift variant) | Autosomal dominant nonsyndromic hearing loss 12 | |
| | TBCEL-TECTA, TECTA (V541M +1 more) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 12 +4 more | GConflicting classifications of pathogenicity |
| | TBCEL-TECTA, TECTA (P1248L +1 more) | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 21 +4 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene