| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +5 more | |
| | | Single nucleotide variant (nonsense +2 more) | Pheochromocytoma +6 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not provided +1 more | |
Click to view in NCBI Gene