| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129389274, CPLANE1 (T1463I) | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | CPLANE1, LOC129389274 (I1426T) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
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