| Disease Name | phenotype | Inheritance Mode | Chr Location | Mutation Type | Gene Name | mRNA Variant | Protein Variant | Effect | Reference |
| Hearing Impairment 97 (DFNB97, MET) | severe sensorineural hearing loss | Autosomal Recessive | 7q31.2 | Missense | MET | 2521T>G | Phe841Val | Amino Acid Substitution | 0/Mujtaba et al., 2015 |
