ClinVar Miner

List of variants in gene PDGFRA studied for not specified

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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_006206.6(PDGFRA):c.3222T>C (p.Asp1074=) rs7685117 0.99715
NM_006206.6(PDGFRA):c.1701A>G (p.Pro567=) rs1873778 0.96449
NM_006206.6(PDGFRA):c.3123-38C>T rs3733540 0.73955
NM_006206.6(PDGFRA):c.2472C>T (p.Val824=) rs2228230 0.20293
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.1432T>C (p.Ser478Pro) rs35597368 0.15258
NM_006206.6(PDGFRA):c.368-3C>T rs55947416 0.04647
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.672G>A (p.Val224=) rs151259376 0.00707
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.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.1731G>A (p.Pro577=) rs55830582 0.00105
NM_006206.6(PDGFRA):c.599C>G (p.Thr200Ser) rs149951350 0.00086
NM_006206.6(PDGFRA):c.*6G>A rs148697831 0.00068
NM_006206.6(PDGFRA):c.2871A>G (p.Gln957=) rs752373446 0.00036
NM_006206.6(PDGFRA):c.2306A>T (p.Lys769Met) rs373061721 0.00032
NM_006206.6(PDGFRA):c.1891+10C>T rs190242331 0.00024
NM_006206.6(PDGFRA):c.1135T>G (p.Leu379Val) rs199827643 0.00014
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.1296G>A (p.Thr432=) rs374217334 0.00007
NM_006206.6(PDGFRA):c.2935C>T (p.Arg979Cys) rs587778597 0.00006
NM_006206.6(PDGFRA):c.1057A>C (p.Asn353His) rs139103850 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.368-4A>G rs944515268 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.1700_1701inv (p.Pro567Leu)
NM_006206.6(PDGFRA):c.853A>G (p.Ser285Gly) rs541057765

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