| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CCT8, LOC130066508 (T181A +3 more) | Single nucleotide variant (missense variant) | not specified | |
| | CCT8, LOC130066508 (V144L +3 more) | Single nucleotide variant (missense variant) | not specified | |
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