| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130009231, SFSWAP (G28D) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130009231, SFSWAP (G28C) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130009231, SFSWAP (E20A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130009231, SFSWAP (E12K) | Single nucleotide variant (missense variant) | not specified | |
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