| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CAGE1, LOC129389436 (S156R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CAGE1, LOC129389436 (P151S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CAGE1, LOC129389436 (R145W +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CAGE1, LOC129389436 (V254I +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene