| Disease Name | phenotype | Inheritance Mode | Chr Location | Mutation Type | Gene Name | mRNA Variant | Protein Variant | Effect | Reference |
| Hearing Impairment 86 (DFNB86, TBC1D24) | Profound hearing impairment | Autosomal Recessive | 16p13.3 | Missense | TBC1D24 | 208G>T | Asp70Tyr | Amino Acid Substitution | 0/Rehman et al., 2014 |
| Hearing Impairment 86 (DFNB86, TBC1D24) | Profound hearing impairment | Autosomal Recessive | 16p13.3 | Missense | TBC1D24 | 878G>C | Arg293Pro | Amino Acid Substitution | 0/Rehman et al., 2014 |
