| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130001407, PPP1R16A (G306A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130001407, PPP1R16A (E308K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130001407, PPP1R16A (H319N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130001407, PPP1R16A (D322N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130001407, PPP1R16A (G343R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130001407, PPP1R16A (R351W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130001407, PPP1R16A (A369T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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