| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126860242, RBM33 (S731L) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126860242, RBM33 (A702P) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126860242, RBM33 (A740V) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126860242, RBM33 (T729A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126860242, RBM33 (K771E) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126860242, RBM33 (A732T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126860242, RBM33 (T729M) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126860242, RBM33 (R745Q) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126860242, RBM33 (P715A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126860242, RBM33 (V690A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129999714, RBM33 (G1029V) | Single nucleotide variant (missense variant) | not specified | |
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