| Disease Name | phenotype | Inheritance Mode | Chr Location | Mutation Type | Gene Name | mRNA Variant | Protein Variant | Effect | Reference |
| Hearing Impairment 73 (DFNB73, BSND) | severe to profound hearing loss | Autosomal Recessive | 1p32.3 | Missense | BSND | 35T>C | Ile12Thr | Amino Acid Substitution | 0/Riazuddin et al., 2009 |
| Hearing Impairment 73 (DFNB73, BSND) | severe to profound hearing loss | Autosomal Recessive | 1p32.3 | Nonsense | BSND | 10G>T | Glu4* | Premature Termination | 0/Riazuddin et al., 2009 |
| Hearing Impairment 73 (DFNB73, BSND) | severe to profound hearing loss | Autosomal Recessive | 1p32.3 | Missense | BSND | c.97G>C | Val33Leu | Amino acid substitution | 2014/Shafique et al. 2014 |
