| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Adrenocortical carcinoma, hereditary +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Adrenocortical carcinoma, hereditary +14 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Adrenocortical carcinoma, hereditary +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Li-Fraumeni syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Glioma susceptibility 1 +14 more | GConflicting classifications of pathogenicity |
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