| | TBCEL-TECTA, TECTA (I1102M +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (G1104V +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TECTA, TBCEL-TECTA (C260F +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | TBCEL-TECTA, TECTA (G390R +1 more) | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 21 | |
| | | Single nucleotide variant (intron variant) | Autosomal dominant nonsyndromic hearing loss 12 +1 more | |
| | TBCEL-TECTA, TECTA (S2120T +1 more) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 12 +1 more | |
| | TBCEL-TECTA, TECTA (D505H +1 more) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 12 +1 more | |
| | TBCEL-TECTA, TECTA (T1976P +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (V415I +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (I1846S +1 more) | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 21 | |
| | TBCEL-TECTA, TECTA (M1811del +1 more) | Deletion | Nonsyndromic genetic hearing loss | |
| | TECTA, TBCEL-TECTA (K1726N +1 more) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 12 | |
| | TBCEL-TECTA, TECTA (D361E +1 more) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 12 | |
| | TBCEL-TECTA, TECTA (N455S +1 more) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 12 | |
| | TBCEL-TECTA, TECTA (N1538S +1 more) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 12 | |
| | TBCEL-TECTA, TECTA (V1182I +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (T280A +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (C1622R +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (C1427Y +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (splice donor variant) | Autosomal recessive nonsyndromic hearing loss 21 | |
| | TBCEL-TECTA, TECTA (C1408* +1 more) | Single nucleotide variant (nonsense) | Autosomal recessive nonsyndromic hearing loss 21 | |
| | | Single nucleotide variant (synonymous variant) | not specified | |
| | TECTA, TBCEL-TECTA (G1478F +1 more) | Indel (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (D511E +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (P1133R +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (C1704S +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (E1715G +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (G1492R +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (I1868F +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (E1148K +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126861365, TBCEL-TECTA +1 more (D1210G +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (E1901K +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (V1963F +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (C1464S +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (V2026D +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | LOC126861365, TBCEL-TECTA +1 more (R1278W +1 more) | Single nucleotide variant (missense variant) | TECTA-related disorder | |
| | | Single nucleotide variant (intron variant) | TECTA-related disorder | |
| | TBCEL-TECTA, TECTA (T261A +1 more) | Single nucleotide variant (missense variant) | TECTA-related disorder | |
| | TBCEL-TECTA, TECTA (D102N +1 more) | Single nucleotide variant (missense variant) | TECTA-related disorder | |
| | TBCEL-TECTA, TECTA (S158fs +1 more) | Duplication (frameshift variant) | TECTA-related disorder | |
| | TBCEL-TECTA, TECTA (W100R +1 more) | Single nucleotide variant (missense variant) | TECTA-related disorder | |
| | TBCEL-TECTA, TECTA (G2078R +1 more) | Single nucleotide variant (missense variant) | TECTA-related disorder | |
| | TBCEL-TECTA, TECTA (E1998G +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (E291D +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (Q442fs +1 more) | Deletion (frameshift variant) | not provided | |
| | TBCEL-TECTA, TECTA (A1982D +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | TBCEL-TECTA, TECTA (Y1900C +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Hearing impairment | |
| | TBCEL-TECTA, TECTA (V1384fs +1 more) | Deletion (frameshift variant) | not provided | |
| | TBCEL-TECTA, TECTA (A16T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (D553E +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (T1482S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (K1609M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (G1738W +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (V1618A +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (P646R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (T192M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861365, TBCEL-TECTA +1 more (E1195Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861365, TBCEL-TECTA +1 more (G1291E +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (T1446A +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (F2027V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (R1150Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (H1944R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (L409F +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (T546I +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (E2326K +1 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | LOC126861365, TBCEL-TECTA +1 more | Single nucleotide variant (synonymous variant) | not provided | |
| | TBCEL-TECTA, TECTA (T165I +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (C1619Y +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | TBCEL-TECTA, TECTA (E1015K +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126861365, TBCEL-TECTA +1 more (A1191S +1 more) | Single nucleotide variant (missense variant) | Autosomal recessive nonsyndromic hearing loss 21 | |
| | TBCEL-TECTA, TECTA (G434V +1 more) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 12 | |
| | TBCEL-TECTA, TECTA (F406C +1 more) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 12 | |
| | TBCEL-TECTA, TECTA (D1769Y +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | TBCEL-TECTA, TECTA (R1243C +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126861365, TBCEL-TECTA +1 more | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | TBCEL-TECTA, TECTA (R268Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (T536I +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (E2403K +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (V2391L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (E2383D +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (N2195D +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (E1776K +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (D173N +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (L1472M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (P1706L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (N1306I +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (N1245S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (S1551N +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TBCEL-TECTA, TECTA (V1218I +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |