| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126862183, SCAPER (P953L +4 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126862183, SCAPER (R1068Q +4 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126862183, SCAPER (G792E +4 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene