| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130000102, PNOC (E110K +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130000102, PNOC (E112K +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130000102, PNOC (Q44K +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130000102, PNOC (Q125H +1 more) | Single nucleotide variant (missense variant) | not specified | |
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