U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PDGFRA
(A280S +2 more)
Single nucleotide variant
(missense variant)
Gastrointestinal stromal tumor
+3 more
GUncertain significance
PDGFRA
(R293H +2 more)
Single nucleotide variant
(missense variant)
Idiopathic hypereosinophilic syndrome
+3 more
GUncertain significance
PDGFRA
(L379V +2 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
PDGFRA
(H425R +2 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+5 more
GUncertain significance
PDGFRA
(L442P +2 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
PDGFRA
(Q551K +2 more)
Single nucleotide variant
(missense variant)
Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal
+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)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
PDGFRA
(I989V +2 more)
Single nucleotide variant
(missense variant)
Gastrointestinal stromal tumor
+4 more
GConflicting classifications of pathogenicity
PDGFRA
(I1067T +2 more)
Single nucleotide variant
(missense variant)
Idiopathic hypereosinophilic syndrome
+2 more
GUncertain significance
Format
Items per page
Sort by
Choose Destination