NM_006206.6(PDGFRA):c.368-3C>T
|
rs55947416
|
0.04647
|
NM_006206.6(PDGFRA):c.*2504C>T
|
rs149631103
|
0.00967
|
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_006206.5(PDGFRA):c.-170C>T
|
rs183431225
|
0.00310
|
NM_006206.6(PDGFRA):c.661C>T (p.Leu221Phe)
|
rs139913632
|
0.00307
|
NM_006206.6(PDGFRA):c.996C>T (p.Val332=)
|
rs142498442
|
0.00204
|
NM_006206.6(PDGFRA):c.1122G>C (p.Arg374Ser)
|
rs61735622
|
0.00183
|
NM_006206.5(PDGFRA):c.-284G>A
|
rs145549583
|
0.00121
|
NM_006206.6(PDGFRA):c.*2538G>A
|
rs377126983
|
0.00095
|
NM_006206.6(PDGFRA):c.*2873C>T
|
rs147418921
|
0.00087
|
NM_006206.6(PDGFRA):c.599C>G (p.Thr200Ser)
|
rs149951350
|
0.00086
|
NM_006206.6(PDGFRA):c.*2100A>G
|
rs192159089
|
0.00083
|
NM_006206.6(PDGFRA):c.*2546A>G
|
rs112690644
|
0.00081
|
NM_006206.6(PDGFRA):c.3228C>T (p.Ile1076=)
|
rs148629782
|
0.00076
|
NM_006206.5(PDGFRA):c.*2973+14G>A
|
rs137930765
|
0.00074
|
NM_006206.6(PDGFRA):c.3156G>A (p.Thr1052=)
|
rs55996208
|
0.00064
|
NM_006206.6(PDGFRA):c.1285G>A (p.Gly429Arg)
|
rs150577828
|
0.00034
|
NM_006206.6(PDGFRA):c.*1561T>C
|
rs145328998
|
0.00025
|
NM_006206.6(PDGFRA):c.*1778C>A
|
rs182602738
|
0.00019
|
NM_006206.6(PDGFRA):c.1135T>G (p.Leu379Val)
|
rs199827643
|
0.00014
|
NM_006206.6(PDGFRA):c.2942G>A (p.Arg981His)
|
rs368266633
|
0.00010
|
NM_006206.6(PDGFRA):c.17C>T (p.Pro6Leu)
|
rs754092062
|
0.00009
|
NM_006206.6(PDGFRA):c.*2465A>G
|
rs78148538
|
0.00006
|
NM_006206.6(PDGFRA):c.896T>C (p.Val299Ala)
|
rs200033396
|
0.00006
|
NM_006206.6(PDGFRA):c.*2256G>T
|
rs544503522
|
0.00004
|
NM_006206.6(PDGFRA):c.2897A>G (p.His966Arg)
|
rs200042995
|
0.00004
|
NM_006206.6(PDGFRA):c.3039C>T (p.Ser1013=)
|
rs138150216
|
0.00004
|
NM_006206.6(PDGFRA):c.1891C>T (p.Pro631Ser)
|
rs199902153
|
0.00003
|
NM_006206.6(PDGFRA):c.*505A>G
|
rs373134586
|
0.00001
|
NM_006206.6(PDGFRA):c.*793C>T
|
rs557191329
|
0.00001
|
NM_006206.6(PDGFRA):c.1471G>A (p.Ala491Thr)
|
rs563016888
|
0.00001
|
NM_006206.6(PDGFRA):c.2266G>A (p.Asp756Asn)
|
rs555347387
|
0.00001
|
NM_006206.6(PDGFRA):c.3191A>G (p.Asp1064Gly)
|
rs375050626
|
0.00001
|
NM_006206.6(PDGFRA):c.3228C>G (p.Ile1076Met)
|
rs148629782
|
|
NM_006206.6(PDGFRA):c.853A>G (p.Ser285Gly)
|
rs541057765
|
|