| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CENPP, OGN (G161S +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CENPP, OGN (D157E +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CENPP, OGN (P241S +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CENPP, OGN (R264W +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CENPP, OGN (K133Q +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CENPP, OGN (P176A +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CENPP, OGN (A136V +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CENPP, OGN (N125K +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CENPP, OGN (H222R +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CENPP, OGN (P139L +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CENPP, OGN (A180T +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
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