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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PDGFRA
(A280S +2 more)
Single nucleotide variant
(missense variant)
Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal
+3 more
GUncertain significance
PDGFRA
(R293H +2 more)
Single nucleotide variant
(missense variant)
Gastrointestinal stromal tumor
+3 more
GUncertain significance
PDGFRA
(L379V +2 more)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
PDGFRA
(H425R +2 more)
Single nucleotide variant
(missense variant)
Gastrointestinal stromal tumor
+4 more
GUncertain significance
PDGFRA
(L442P +2 more)
Single nucleotide variant
(missense variant)
Gastrointestinal stromal tumor
+3 more
GConflicting classifications of pathogenicity
PDGFRA
(Q551K +2 more)
Single nucleotide variant
(missense variant)
Gastrointestinal stromal tumor
+2 more
GUncertain significance
PDGFRA
(P553L +2 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GUncertain significance
PDGFRA
(I657T +2 more)
Single nucleotide variant
(missense variant)
Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal
+3 more
GConflicting classifications of pathogenicity
PDGFRA
(I989V +2 more)
Single nucleotide variant
(missense variant)
Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal
+4 more
GConflicting classifications of pathogenicity
PDGFRA
(I1067T +2 more)
Single nucleotide variant
(missense variant)
Gastrointestinal stromal tumor
+2 more
GUncertain significance
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