List of variants in gene PDGFRA reported as not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_006206.6(PDGFRA):c.1432T>C (p.Ser478Pro)	rs35597368	0.15258
NM_006206.6(PDGFRA):c.1019G>A (p.Arg340Gln)	rs77524207	0.01633
NM_006206.6(PDGFRA):c.236G>A (p.Gly79Asp)	rs36035373	0.00897
NM_006206.6(PDGFRA):c.661C>T (p.Leu221Phe)	rs139913632	0.00307
NM_006206.6(PDGFRA):c.2230C>T (p.Pro744Ser)	rs61735626	0.00206
NM_006206.6(PDGFRA):c.1122G>C (p.Arg374Ser)	rs61735622	0.00183
NM_006206.6(PDGFRA):c.2899C>G (p.Leu967Val)	rs140943817	0.00150
NM_006206.6(PDGFRA):c.2282T>G (p.Leu761Arg)	rs148654387	0.00126
NM_006206.6(PDGFRA):c.599C>G (p.Thr200Ser)	rs149951350	0.00086
NM_006206.6(PDGFRA):c.3155C>T (p.Thr1052Met)	rs397514550	0.00034
NM_006206.6(PDGFRA):c.2306A>T (p.Lys769Met)	rs373061721	0.00032
NM_006206.6(PDGFRA):c.1631T>C (p.Val544Ala)	rs181854060	0.00012
NM_006206.6(PDGFRA):c.499G>A (p.Val167Met)	rs587778602	0.00008
NM_006206.6(PDGFRA):c.2935C>T (p.Arg979Cys)	rs587778597	0.00006
NM_006206.6(PDGFRA):c.3179T>A (p.Ile1060Asn)	rs774522904	0.00005
NM_006206.6(PDGFRA):c.1057A>C (p.Asn353His)	rs139103850	0.00003
NM_006206.6(PDGFRA):c.899A>C (p.Lys300Thr)	rs368648130	0.00003
NM_006206.6(PDGFRA):c.97A>T (p.Asn33Tyr)	rs200979664	0.00003
NM_006206.6(PDGFRA):c.2936G>A (p.Arg979His)	rs587778598	0.00002
NM_006206.6(PDGFRA):c.1307C>T (p.Thr436Ile)	rs139920579	0.00001
NM_006206.6(PDGFRA):c.2966T>C (p.Ile989Thr)	rs587778599	0.00001
NM_006206.6(PDGFRA):c.46A>T (p.Thr16Ser)	rs587778596	0.00001
NM_006206.6(PDGFRA):c.86C>T (p.Ser29Phe)	rs587778600	0.00001
NM_006206.6(PDGFRA):c.1357A>T (p.Ile453Phe)	rs587778603
NM_006206.6(PDGFRA):c.1417A>G (p.Ile473Val)	rs587778594
NM_006206.6(PDGFRA):c.167G>C (p.Ser56Thr)	rs587778601
NM_006206.6(PDGFRA):c.1682T>C (p.Val561Ala)	rs121908586
NM_006206.6(PDGFRA):c.1700_1701inv (p.Pro567Leu)
NM_006206.6(PDGFRA):c.853A>G (p.Ser285Gly)	rs541057765

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