| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130058894, PRSS36 (A492E) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058894, PRSS36 (G469S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058894, PRSS36 (G441R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058894, PRSS36 (P484S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058894, PRSS36 (G468D) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058894, PRSS36 (L475Q) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058894, PRSS36 (A424G) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130058894, PRSS36 (C506G) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC130058894, PRSS36 (E502D) | Single nucleotide variant (missense variant) | not specified | |
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