| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LAPTM5, LOC129929973 (R4G) | Single nucleotide variant (missense variant) | not specified | |
| | LAPTM5, LOC129929973 (R4H) | Single nucleotide variant (missense variant) | not specified | |
| | LAPTM5, LOC129929973 (R18C) | Single nucleotide variant (missense variant) | not specified | |
| | LAPTM5, LOC129929973 (R4C) | Single nucleotide variant (missense variant) | not specified | |
| | LAPTM5, LOC129929973 (R4P) | Single nucleotide variant (missense variant) | not specified | |
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