| | LOC129932799, TARBP1 (W263R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TARBP1, LOC129932799 (R261P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (P244L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (A235G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (V226G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (G222R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (G193R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (A188V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (G182R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (G174R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (A169T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (R162L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TARBP1, LOC129932799 (R162G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (A145P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (P114L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (R105H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (R93S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (R91C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (L88M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (R77S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (S75R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (A28V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (Q25E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (R17Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (R14W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129932799, TARBP1 (Q12H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |