| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126861119, TRIM5 (V134I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861119, TRIM5 (C95S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861119, TRIM5 (R71Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126861119, TRIM5 (R71W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene