List of variants in gene PDGFRA studied for cancer

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_006206.6(PDGFRA):c.1701A>G (p.Pro567=)	rs1873778	0.96449
NM_006206.6(PDGFRA):c.2440-50_2440-49insA	rs3830355	0.75180
NM_006206.6(PDGFRA):c.1432T>C (p.Ser478Pro)	rs35597368	0.15258
NM_006206.6(PDGFRA):c.661C>T (p.Leu221Phe)	rs139913632	0.00307
NM_006206.6(PDGFRA):c.1631T>C (p.Val544Ala)	rs181854060	0.00012
NM_006206.6(PDGFRA):c.1202C>A (p.Ala401Asp)	rs397514549	0.00010
NM_006206.6(PDGFRA):c.2942G>A (p.Arg981His)	rs368266633	0.00010
NM_006206.6(PDGFRA):c.1319C>T (p.Thr440Met)	rs143344944	0.00009
NM_006206.6(PDGFRA):c.17C>T (p.Pro6Leu)	rs754092062	0.00009
NM_006206.6(PDGFRA):c.248C>T (p.Thr83Met)	rs779332376	0.00009
NM_006206.6(PDGFRA):c.516C>T (p.Tyr172=)	rs1046079554	0.00002
NM_006206.6(PDGFRA):c.2119A>G (p.Ile707Val)	rs1318827602	0.00001
NM_006206.6(PDGFRA):c.3098A>T (p.Asp1033Val)	rs201874958	0.00001
NM_006206.6(PDGFRA):c.167G>C (p.Ser56Thr)	rs587778601
NM_006206.6(PDGFRA):c.2315C>A (p.Ser772Tyr)	rs1577735147
NM_006206.6(PDGFRA):c.334C>T (p.Leu112Phe)	rs1722706795
NM_006206.6(PDGFRA):c.35G>C (p.Gly12Ala)	rs1440200916

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