| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | PARD6G, PARD6G-AS1 (N327S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PARD6G, PARD6G-AS1 (F288V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PARD6G, PARD6G-AS1 (V256L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PARD6G, PARD6G-AS1 (I303V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130062804, PARD6G +1 more (V374F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PARD6G, PARD6G-AS1 (P309R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PARD6G, PARD6G-AS1 (R337W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PARD6G-AS1, PARD6G (D271E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PARD6G, PARD6G-AS1 (L360V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PARD6G, PARD6G-AS1 (R181C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PARD6G-AS1, PARD6G (G125V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PARD6G, PARD6G-AS1 (G272R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PARD6G, PARD6G-AS1 (L121R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Copy number loss | not provided | |
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