| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126807040, RBM47 (Q506H +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126807040, RBM47 (G469R +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126807040, RBM47 (V520F +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126807040, RBM47 (Y522H +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126807040, RBM47 (P509S +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126807040, RBM47 (A507T +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126807040, RBM47 (N520K +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126807040, RBM47 (N558K +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126807040, RBM47 (P549L +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126807040, RBM47 (Y499C +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126807040, RBM47 (I449V +2 more) | Single nucleotide variant (missense variant) | not specified | |
Click to view in NCBI Gene