| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CCT6A, LOC121175344 (M487T +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CCT6A, LOC129998497 (A14V) | Single nucleotide variant (missense variant) | not specified | |
| | CCT6A, LOC121175344 (M487V +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CCT6A, LOC121175344 (P486T +1 more) | Single nucleotide variant (missense variant) | not specified | |
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