| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ARPC5, LOC129932089 (T5fs) | Insertion (frameshift variant) | Immunodeficiency 113 with autoimmunity and autoinflammation | |
| | | Single nucleotide variant (nonsense) | Immunodeficiency 113 with autoimmunity and autoinflammation | |
| | ARPC5, LOC129932089 (D32E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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