| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC121099717, PRR7 (P117T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129995383, PRR7 (T244N) | Single nucleotide variant (missense variant) | not specified | |
| | LOC121099717, PRR7 (H104Q) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | LOC121099717, PRR7 (P123R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC121099717, PRR7 (H124Q) | Single nucleotide variant (missense variant) | not specified | |
| | LOC121099717, PRR7 (P127S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129995383, PRR7 (P220H) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129995383, PRR7 (S249N) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
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