| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Nephrotic syndrome, type 6 | |
| | LOC126861467, PTPRO (P695A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Nephrotic syndrome, type 6 | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | LOC126861467, PTPRO (G710R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Nephrotic syndrome, type 6 +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Duplication (frameshift variant) | not provided | |
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