| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | TBCEL-TECTA, TECTA (T165S +1 more) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 12 | |
| | TBCEL-TECTA, TECTA (C671Y +1 more) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 12 | |
| | LOC126861365, TBCEL-TECTA
+1 more | Single nucleotide variant (synonymous variant) | Autosomal recessive nonsyndromic hearing loss 21 | |
| | TECTA, TBCEL-TECTA (G1257S +1 more) | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Microsatellite (splice donor variant) | Bilateral sensorineural hearing impairment +2 more | |
| | TBCEL-TECTA, TECTA (T1866M +1 more) | Single nucleotide variant (missense variant) | Rare genetic deafness +5 more | GConflicting classifications of pathogenicity |
| | TBCEL-TECTA, TECTA (P1914R +1 more) | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 21 | |
| | TBCEL-TECTA, TECTA (E2035* +1 more) | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 21 | |
Click to view in NCBI Gene