| | LOC127814297, POU4F3 (F293L) | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (L201fs) | Deletion (3 prime UTR variant +1 more) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (K275fs) | Deletion (3 prime UTR variant +1 more) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (H165fs) | Deletion (3 prime UTR variant +1 more) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (Q225H) | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (V167M) | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (F293L) | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (L248P) | Single nucleotide variant (3 prime UTR variant +1 more) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (A189fs) | Duplication (frameshift variant +1 more) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (G202R) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (W321fs) | Deletion (frameshift variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (G160fs) | Deletion (frameshift variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (H13fs) | Deletion (frameshift variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (S23fs) | Deletion (frameshift variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (Q249K) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | LOC127814297, POU4F3 (E232*) | Single nucleotide variant (nonsense) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (E18fs) | Deletion (frameshift variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (P125S) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (V318M) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (A257V) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (Q296*) | Single nucleotide variant (nonsense) | not provided | |
| | LOC127814297, POU4F3 (A62fs) | Deletion (frameshift variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (L212P) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (H109Y) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (E232D) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | | Single nucleotide variant (synonymous variant) | Autosomal dominant nonsyndromic hearing loss 15 +1 more | GConflicting classifications of pathogenicity |
| | LOC127814297, POU4F3 (G202A) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (L201P) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 +1 more | GConflicting classifications of pathogenicity |
| | LOC127814297, POU4F3 (H170Y) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | | Single nucleotide variant (synonymous variant) | Autosomal dominant nonsyndromic hearing loss 15 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Autosomal dominant nonsyndromic hearing loss 15 +1 more | GConflicting classifications of pathogenicity |
| | LOC127814297, POU4F3 (A61E) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (H109Q) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (H99Y) | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Autosomal dominant nonsyndromic hearing loss 15 +1 more | GConflicting classifications of pathogenicity |
| | LOC127814297, POU4F3 (H72D) | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | LOC127814297, POU4F3 (S171R) | Single nucleotide variant (missense variant) | not specified +3 more | |
| | LOC127814297, POU4F3 (R185C) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (A168fs) | Deletion (frameshift variant) | Autosomal dominant nonsyndromic hearing loss 15 +1 more | GPathogenic/Likely pathogenic |
| | LOC127814297, POU4F3 (N316K) | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Autosomal dominant nonsyndromic hearing loss 15 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (R193C) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (H148Y) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 +2 more | |
| | LOC127814297, POU4F3 (A38D) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | | Single nucleotide variant (5 prime UTR variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | | Single nucleotide variant (5 prime UTR variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | Autosomal dominant nonsyndromic hearing loss 15 +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | LOC127814297, POU4F3 (P135S) | Single nucleotide variant (missense variant) | not specified +2 more | |
| | LOC127814297, POU4F3 (G221fs) | Deletion (frameshift variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (R326K) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | LOC127814297, POU4F3 (L223P) | Single nucleotide variant (missense variant) | not provided | |
| | LOC127814297, POU4F3 (L289F) | Single nucleotide variant (missense variant) | Autosomal dominant nonsyndromic hearing loss 15 | |
| | LOC127814297, POU4F3 (I295fs) | Deletion (frameshift variant) | Autosomal dominant nonsyndromic hearing loss 15 | |