| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC111946221, TUBGCP2
+2 more (L7M) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC111946221, TUBGCP2
+2 more (R10C) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC111946221, TUBGCP2
+2 more (Q62P) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC111946221, TUBGCP2
+2 more (Q62H) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC111946221, TUBGCP2
+2 more (M66V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
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