List of variants in gene PDGFRA reported as likely pathogenic for Gastrointestinal stromal tumor

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_006206.6(PDGFRA):c.1664A>G (p.Tyr555Cys)	rs121908589
NM_006206.6(PDGFRA):c.2522_2527del (p.Arg841_Asp842del)	rs121913269
NM_006206.6(PDGFRA):c.2524G>T (p.Asp842Tyr)	rs121913265
NM_006206.6(PDGFRA):c.2524_2525delinsAT (p.Asp842Ile)	rs121913264
NM_006206.6(PDGFRA):c.2524_2532del (p.Asp842_Met844del)	rs121913262
NM_006206.6(PDGFRA):c.2526_2537del (p.Ile843_Asp846del)	rs1553906053
NM_006206.6(PDGFRA):c.2527_2538del (p.Ile843_Asp846del)	rs121913267
NM_006206.6(PDGFRA):c.2536G>T (p.Asp846Tyr)	rs121908588
NM_006206.6(PDGFRA):c.451C>T (p.Arg151Cys)	rs1449637193

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