List of variants in gene PDGFRA reported as likely benign for 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: 42

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HGVS	dbSNP	gnomAD frequency
NM_006206.6(PDGFRA):c.2674+147T>C	rs111854300	0.01428
NM_006206.6(PDGFRA):c.2157-250T>A	rs28595114	0.01420
NM_006206.6(PDGFRA):c.2323+287del	rs532763191	0.01347
NM_006206.6(PDGFRA):c.*2504C>T	rs149631103	0.00967
NM_006206.6(PDGFRA):c.2675-105G>C	rs142125556	0.00863
NM_006206.6(PDGFRA):c.1121+35T>A	rs530577459	0.00832
NM_006206.6(PDGFRA):c.2157-135A>G	rs73252951	0.00802
NM_006206.6(PDGFRA):c.-13+132T>G	rs74962312	0.00731
NM_006206.6(PDGFRA):c.672G>A (p.Val224=)	rs151259376	0.00707
NM_006206.6(PDGFRA):c.2674+336G>A	rs149020631	0.00628
NM_006206.6(PDGFRA):c.1122-66C>T	rs114447107	0.00524
NM_006206.6(PDGFRA):c.201C>T (p.Ser67=)	rs35805947	0.00429
NM_006206.6(PDGFRA):c.2778C>T (p.Tyr926=)	rs138519829	0.00372
NM_006206.6(PDGFRA):c.629-169C>T	rs78684235	0.00334
NM_006206.6(PDGFRA):c.661C>T (p.Leu221Phe)	rs139913632	0.00307
NM_006206.6(PDGFRA):c.3123-112C>G	rs180872904	0.00284
NM_006206.6(PDGFRA):c.996C>T (p.Val332=)	rs142498442	0.00204
NM_006206.6(PDGFRA):c.2282T>G (p.Leu761Arg)	rs148654387	0.00126
NM_006206.6(PDGFRA):c.1731G>A (p.Pro577=)	rs55830582	0.00105
NM_006206.6(PDGFRA):c.3156G>A (p.Thr1052=)	rs55996208	0.00064
NM_006206.6(PDGFRA):c.2871A>G (p.Gln957=)	rs752373446	0.00036
NM_006206.6(PDGFRA):c.276G>A (p.Ala92=)	rs140725151	0.00030
NM_006206.6(PDGFRA):c.801A>G (p.Pro267=)	rs55966236	0.00024
NM_006206.6(PDGFRA):c.1135T>G (p.Leu379Val)	rs199827643	0.00014
NM_006206.6(PDGFRA):c.2205G>A (p.Lys735=)	rs758609201	0.00009
NM_006206.6(PDGFRA):c.738A>G (p.Gln246=)	rs377699966	0.00008
NM_006206.6(PDGFRA):c.2742G>C (p.Arg914=)	rs56384252	0.00006
NM_006206.6(PDGFRA):c.3003G>A (p.Lys1001=)	rs373642812	0.00005
NM_006206.6(PDGFRA):c.1471G>A (p.Ala491Thr)	rs563016888	0.00001
NM_006206.6(PDGFRA):c.2049C>G (p.Val683=)	rs200719395	0.00001
NM_006206.6(PDGFRA):c.46A>T (p.Thr16Ser)	rs587778596	0.00001
NM_006206.6(PDGFRA):c.-13+156dup	rs920838716
NM_006206.6(PDGFRA):c.1296G>C (p.Thr432=)	rs374217334
NM_006206.6(PDGFRA):c.1542G>A (p.Leu514=)	rs1577724676
NM_006206.6(PDGFRA):c.1787-232C>A	rs111624835
NM_006206.6(PDGFRA):c.1892-158A>G	rs116215839
NM_006206.6(PDGFRA):c.2003-117_2003-109del	rs5858262
NM_006206.6(PDGFRA):c.2323+277_2323+278del	rs368963999
NM_006206.6(PDGFRA):c.2323+291del	rs533682086
NM_006206.6(PDGFRA):c.2563-46A>G	rs144143098
NM_006206.6(PDGFRA):c.628+82dup
NM_006206.6(PDGFRA):c.629-68dup	rs61317836

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