| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | KLHL31, LOC129996651 (R566C) | Single nucleotide variant (missense variant) | not specified | |
| | KLHL31, LOC129996652 (E528G) | Single nucleotide variant (missense variant) | not specified | |
| | KLHL31, LOC129996652 (D487V) | Single nucleotide variant (missense variant) | not specified | |
| | KLHL31, LOC129996652 (A478S) | Single nucleotide variant (missense variant) | not specified | |
| | KLHL31, LOC129996652 (Y474H) | Single nucleotide variant (missense variant) | not specified | |
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