ClinVar Miner

List of variants in gene PDGFRA reported as benign for not provided

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Gene type:
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Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_006206.6(PDGFRA):c.2674+213T>C rs7654385 0.99715
NM_006206.6(PDGFRA):c.3222T>C (p.Asp1074=) rs7685117 0.99715
NM_006206.6(PDGFRA):c.*78A>G rs7680422 0.99696
NM_006206.6(PDGFRA):c.1558+134T>G rs1492766 0.98984
NM_006206.6(PDGFRA):c.*2387T>G rs10034498 0.98684
NM_006206.6(PDGFRA):c.1701A>G (p.Pro567=) rs1873778 0.96449
NM_006206.6(PDGFRA):c.1558+81T>C rs1492765 0.96185
NM_006206.6(PDGFRA):c.2674+129A>G rs7695657 0.95550
NM_006206.6(PDGFRA):c.2880+217A>G rs4864873 0.95550
NM_006206.6(PDGFRA):c.2881-100G>A rs4864506 0.95547
NM_006206.6(PDGFRA):c.2003-82T>C rs1907820 0.95431
NM_006206.6(PDGFRA):c.2003-109A>G rs1907819 0.77535
NM_006206.6(PDGFRA):c.2562+154T>G rs4864872 0.75220
NM_006206.6(PDGFRA):c.2440-50_2440-49insA rs3830355 0.75180
NM_006206.6(PDGFRA):c.2881-80A>G rs2276948 0.74063
NM_006206.6(PDGFRA):c.3123-38C>T rs3733540 0.73955
NM_006206.6(PDGFRA):c.2323+277T>A rs1388997 0.72302
NM_006206.6(PDGFRA):c.1558+119T>C rs869978 0.67317
NM_006206.6(PDGFRA):c.2003-116A>C rs4493602 0.43888
NM_006206.6(PDGFRA):c.1787-269G>A rs1316926 0.42858
NM_006206.6(PDGFRA):c.2157-94C>T rs1547904 0.26388
NM_006206.6(PDGFRA):c.-12-333A>G rs9991165 0.23047
NM_006206.6(PDGFRA):c.49+74A>T rs2303430 0.21034
NM_006206.6(PDGFRA):c.2881-314A>G rs4864875 0.20384
NM_006206.6(PDGFRA):c.2675-75T>C rs55732997 0.20340
NM_006206.6(PDGFRA):c.2472C>T (p.Val824=) rs2228230 0.20293
NM_006206.6(PDGFRA):c.2881-180C>T rs4864876 0.19986
NM_006206.6(PDGFRA):c.628+60G>A rs2307049 0.17893
NM_006206.6(PDGFRA):c.612T>C (p.Asn204=) rs2229307 0.17867
NM_006206.6(PDGFRA):c.939T>G (p.Gly313=) rs4358459 0.17704
NM_006206.6(PDGFRA):c.1121+28C>T rs28489067 0.17553
NM_006206.6(PDGFRA):c.1809G>A (p.Ala603=) rs10028020 0.17498
NM_006206.6(PDGFRA):c.1121+51C>T rs28650939 0.17438
NM_006206.6(PDGFRA):c.1237+268T>C rs1565669 0.16904
NM_006206.6(PDGFRA):c.1432T>C (p.Ser478Pro) rs35597368 0.15258
NM_006206.6(PDGFRA):c.1786+153G>A rs2307050 0.15228
NM_006206.6(PDGFRA):c.1787-234C>T rs28374326 0.15105
NM_006206.6(PDGFRA):c.760-204T>C rs73252948 0.14601
NM_006206.6(PDGFRA):c.2323+105C>A rs1547905 0.11476
NM_006206.6(PDGFRA):c.629-292T>G rs58727676 0.10814
NM_006206.6(PDGFRA):c.368-3C>T rs55947416 0.04647
NM_006206.6(PDGFRA):c.2439+162C>T rs73820711 0.04144
NM_006206.6(PDGFRA):c.1121+275G>T rs73252949 0.03760
NM_006206.6(PDGFRA):c.3122+144C>T rs73820712 0.03545
NM_006206.6(PDGFRA):c.932-4A>G rs78405886 0.03447
NM_006206.6(PDGFRA):c.2323+279A>T rs10027698 0.03241
NM_006206.6(PDGFRA):c.-12-157A>G rs73151433 0.01934
NM_006206.6(PDGFRA):c.1019G>A (p.Arg340Gln) rs77524207 0.01633
NM_006206.6(PDGFRA):c.2324-26_2324-25insTTT rs760710479 0.01590
NM_006206.6(PDGFRA):c.2324-30_2324-26del rs386674477 0.01588
NM_006206.6(PDGFRA):c.*2504C>T rs149631103 0.00967
NM_006206.6(PDGFRA):c.236G>A (p.Gly79Asp) rs36035373 0.00897
NM_006206.5(PDGFRA):c.-284G>A rs145549583 0.00121
NM_006206.6(PDGFRA):c.599C>G (p.Thr200Ser) rs149951350 0.00086
NM_006206.6(PDGFRA):c.*2970G>T rs752208389 0.00035
NM_006206.6(PDGFRA):c.*1136C>T
NM_006206.6(PDGFRA):c.*374A>C rs3690
NM_006206.6(PDGFRA):c.-106AG[1] rs1799767
NM_006206.6(PDGFRA):c.-13+111dup rs565335773
NM_006206.6(PDGFRA):c.2003-111_2003-109del rs5858262
NM_006206.6(PDGFRA):c.2003-118_2003-109del rs5858262
NM_006206.6(PDGFRA):c.2003-119_2003-109del rs5858262
NM_006206.6(PDGFRA):c.2157-77_2157-76insTGTAGGTCCCCCAG rs6148442
NM_006206.6(PDGFRA):c.2323+278T>A rs58025349
NM_006206.6(PDGFRA):c.2323+278del rs368963999
NM_006206.6(PDGFRA):c.2439+58C>A rs2412559
NM_006206.6(PDGFRA):c.629-68del rs61317836
NM_006206.6(PDGFRA):c.629-69_629-68del rs61317836
NM_006206.6(PDGFRA):c.759+234C>A rs7688997

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