| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130004634, TAF5 (R105Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130004634, TAF5 (G140S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130004634, TAF5 (P156S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130004634, TAF5 (A160V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130004634, TAF5 (P184S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene