| Disease Name | phenotype | Inheritance Mode | Chr Location | Mutation Type | Gene Name | mRNA Variant | Protein Variant | Effect | Reference |
| Hearing Impairment 79 (DFNB79, TPRN) | severe to profound hearing loss | Autosomal Recessive | 9q34.3 | Duplication | TPRN | 44_54Dup | Leu19Glyfs*374 | Frame shift mutation & PTC | 0/Rehman et al., 2010 |
| Hearing Impairment 79 (DFNB79, TPRN) | severe to profound hearing loss | Autosomal Recessive | 9q34.3 | Deletion | TPRN | 42_52del | Gly15Alafs*150 | Frame shift mutation & PTC | 0/Rehman et al., 2010 |
| Hearing Impairment 79 (DFNB79, TPRN) | severe to profound hearing loss | Autosomal Recessive | 9q34.3 | Deletion | TPRN | 1244delC | Pro415Argfs*67 | Frame shift mutation & PTC | 0/Rehman et al., 2010 |
| Hearing Impairment 79 (DFNB79, TPRN) | severe to profound hearing loss | Autosomal Recessive | 9q34.3 | Nonsense | TPRN | 1056G>A | Trp352* | Premature Termination | 0/Rehman et al., 2010 |
| Hearing Impairment 79 (DFNB79, TPRN) | severe to profound hearing loss | Autosomal Recessive | 9q34.3 | Deletion | TPRN | 42_52del11 | Gly15Alafs*150 | Frame shift mutation & PTC | 0/Bashir et al., 2013 |
