| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | ACTG1, LOC130061940 (F31V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ACTG1, LOC130061940 (A29V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ACTG1, LOC130061940 (G23R) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ACTG1, LOC130061940 (C17Y) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene