| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130056344, RIN3 (S93L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC125078025, RIN3 (E813G +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130056351, RIN3 (M572I +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130056344, RIN3 (S109L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC125078025, RIN3 (C856Y +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130056351, RIN3 (Q567P +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC125078025, RIN3 (P865L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC125078025, RIN3 (R842W +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC125078025, RIN3 (G929R +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130056351, RIN3 (M572V +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC125078025, RIN3 (S950R +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number loss | not provided | |
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