ClinVar Miner

List of variants in gene PDGFRA reported as not provided

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Total variants: 27
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HGVS dbSNP
NM_001347827.1(PDGFRA):c.2345C>T (p.Thr782Met) rs2291591
NM_006206.5(PDGFRA):c.1019G>A (p.Arg340Gln) rs77524207
NM_006206.5(PDGFRA):c.1057A>C (p.Asn353His) rs139103850
NM_006206.5(PDGFRA):c.1122G>C (p.Arg374Ser) rs61735622
NM_006206.5(PDGFRA):c.1307C>T (p.Thr436Ile) rs139920579
NM_006206.5(PDGFRA):c.1357A>T (p.Ile453Phe) rs587778603
NM_006206.5(PDGFRA):c.1417A>G (p.Ile473Val) rs587778594
NM_006206.5(PDGFRA):c.1432T>C (p.Ser478Pro) rs35597368
NM_006206.5(PDGFRA):c.1631T>C (p.Val544Ala) rs181854060
NM_006206.5(PDGFRA):c.167G>C (p.Ser56Thr) rs587778601
NM_006206.5(PDGFRA):c.1682T>C (p.Val561Ala) rs121908586
NM_006206.5(PDGFRA):c.1700_1701invCA (p.Pro567Leu)
NM_006206.5(PDGFRA):c.2230C>T (p.Pro744Ser) rs61735626
NM_006206.5(PDGFRA):c.2282T>G (p.Leu761Arg) rs148654387
NM_006206.5(PDGFRA):c.2306A>T (p.Lys769Met) rs373061721
NM_006206.5(PDGFRA):c.236G>A (p.Gly79Asp) rs36035373
NM_006206.5(PDGFRA):c.2899C>G (p.Leu967Val) rs140943817
NM_006206.5(PDGFRA):c.2935C>T (p.Arg979Cys) rs587778597
NM_006206.5(PDGFRA):c.2936G>A (p.Arg979His) rs587778598
NM_006206.5(PDGFRA):c.2966T>C (p.Ile989Thr) rs587778599
NM_006206.5(PDGFRA):c.46A>T (p.Thr16Ser) rs587778596
NM_006206.5(PDGFRA):c.499G>A (p.Val167Met) rs587778602
NM_006206.5(PDGFRA):c.599C>G (p.Thr200Ser) rs149951350
NM_006206.5(PDGFRA):c.661C>T (p.Leu221Phe) rs139913632
NM_006206.5(PDGFRA):c.853A>G (p.Ser285Gly) rs541057765
NM_006206.5(PDGFRA):c.86C>T (p.Ser29Phe) rs587778600
NM_006206.5(PDGFRA):c.97A>T (p.Asn33Tyr) rs200979664

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