| | | Single nucleotide variant (missense variant) | Gastrointestinal stromal tumor +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Gastrointestinal stromal tumor +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Myeloproliferative neoplasm, unclassifiable +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Idiopathic hypereosinophilic syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Gastrointestinal stromal tumor +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic hypereosinophilic syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Gastrointestinal stromal tumor +4 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Gastrointestinal stromal tumor | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Gastrointestinal stromal tumor +3 more | GConflicting classifications of pathogenicity |
| | | Inversion (missense variant) | Gastrointestinal stromal tumor +1 more | |
| | | Single nucleotide variant (missense variant) | Gastrointestinal stromal tumor +1 more | |
| | | Single nucleotide variant (missense variant) | Gastrointestinal stromal tumor +2 more | |
| | | Single nucleotide variant (missense variant) | Gastrointestinal stromal tumor +2 more | GConflicting classifications of pathogenicity |
| | LOC126807054, PDGFRA (T782M) | Single nucleotide variant (missense variant +1 more) | Myeloproliferative neoplasm, unclassifiable +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Gastrointestinal stromal tumor +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | PDGFRA-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Gastrointestinal stromal tumor +1 more | |