| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CCSAP, LOC129932727 (A113T) | Single nucleotide variant (missense variant) | not specified | |
| | CCSAP, LOC129932727 (P101L) | Single nucleotide variant (missense variant) | not specified | |
| | CCSAP, LOC129932727 (S66A) | Single nucleotide variant (missense variant) | not specified | |
| | CCSAP, LOC129932727 (G71D) | Single nucleotide variant (missense variant) | not specified | |
| | CCSAP, LOC129932727 (G109R) | Single nucleotide variant (missense variant) | not specified | |
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