| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126861116, TRIM21 (P319S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861116, TRIM21 (Q316K) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861116, TRIM21 (R306W) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861116, TRIM21 (W299R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861116, TRIM21 (D294N) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861116, TRIM21 (T284S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861116, TRIM21 (R283S) | Single nucleotide variant (missense variant) | not specified | |
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