| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC112042780, TRIM29 (D415N +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC112042780, TRIM29 (R161C +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC112042780, TRIM29 (G149D +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC112042780, TRIM29 (R173C +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC112042780, TRIM29 (A169V +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC112042780, TRIM29 (M166I +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC112042780, TRIM29 (R173P +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC112042780, TRIM29 (V424I +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
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