NM_004239.4(TRIP11):c.5479G>A (p.Gly1827Ser)
|
rs1051340
|
0.29281
|
NM_004239.4(TRIP11):c.115A>T (p.Met39Leu)
|
rs17127898
|
0.06056
|
NM_004239.4(TRIP11):c.4812T>C (p.Asp1604=)
|
rs17127837
|
0.02457
|
NM_004239.4(TRIP11):c.405T>C (p.Ala135=)
|
rs77981249
|
0.01569
|
NM_004239.4(TRIP11):c.5781G>A (p.Ser1927=)
|
rs3742719
|
0.01567
|
NM_004239.4(TRIP11):c.4727G>A (p.Arg1576His)
|
rs35007347
|
0.01467
|
NM_004239.4(TRIP11):c.2651A>G (p.Asp884Gly)
|
rs34967261
|
0.01405
|
NM_004239.4(TRIP11):c.3306T>C (p.Phe1102=)
|
rs34151071
|
0.01402
|
NM_004239.4(TRIP11):c.1527+6A>G
|
rs17127844
|
0.01376
|
NM_004239.4(TRIP11):c.2931C>T (p.Thr977=)
|
rs7152887
|
0.01366
|
NM_004239.4(TRIP11):c.2383G>C (p.Val795Leu)
|
rs34699762
|
0.01322
|
NM_004239.4(TRIP11):c.202-7T>A
|
rs56034853
|
0.01303
|
NM_004239.4(TRIP11):c.3118A>G (p.Ile1040Val)
|
rs34805848
|
0.01111
|
NM_004239.4(TRIP11):c.3714G>A (p.Glu1238=)
|
rs34919898
|
0.01101
|
NM_004239.4(TRIP11):c.5160+59A>G
|
rs117502191
|
0.00901
|
NM_004239.4(TRIP11):c.5651A>G (p.His1884Arg)
|
rs74071672
|
0.00895
|
NM_004239.4(TRIP11):c.2134G>A (p.Glu712Lys)
|
rs143524436
|
0.00835
|
NM_004239.4(TRIP11):c.1517A>C (p.Glu506Ala)
|
rs2273186
|
0.00816
|
NM_004239.4(TRIP11):c.3147G>A (p.Leu1049=)
|
rs17127842
|
0.00729
|
NM_004239.4(TRIP11):c.4164C>T (p.His1388=)
|
rs140130380
|
0.00687
|
NM_004239.4(TRIP11):c.4507A>G (p.Met1503Val)
|
rs34839498
|
0.00686
|
NM_004239.4(TRIP11):c.2217T>C (p.Tyr739=)
|
rs35009380
|
0.00682
|
NM_004239.4(TRIP11):c.3858G>A (p.Gln1286=)
|
rs35798420
|
0.00558
|
NM_004239.4(TRIP11):c.1904C>G (p.Ser635Cys)
|
rs59635749
|
0.00410
|
NM_004239.4(TRIP11):c.5086G>A (p.Glu1696Lys)
|
rs80200454
|
0.00410
|
NM_004239.4(TRIP11):c.3604A>C (p.Asn1202His)
|
rs41301481
|
0.00236
|
NM_004239.4(TRIP11):c.5137G>C (p.Glu1713Gln)
|
rs137974620
|
0.00232
|
NM_004239.4(TRIP11):c.2102A>G (p.Asn701Ser)
|
rs139539448
|
0.00217
|
NM_004239.4(TRIP11):c.5629C>A (p.Pro1877Thr)
|
rs148261539
|
0.00204
|
NM_004239.4(TRIP11):c.4413A>C (p.Thr1471=)
|
rs144780536
|
0.00202
|
NM_004239.4(TRIP11):c.5246A>C (p.Glu1749Ala)
|
rs2273183
|
0.00188
|
NM_004239.4(TRIP11):c.5298G>T (p.Lys1766Asn)
|
rs145868557
|
0.00148
|
NM_004239.4(TRIP11):c.-61C>T
|
rs78222479
|
0.00145
|
NM_004239.4(TRIP11):c.382G>T (p.Ala128Ser)
|
rs141553918
|
0.00133
|
NM_004239.4(TRIP11):c.5010T>C (p.Ala1670=)
|
rs149334552
|
0.00103
|
NM_004239.4(TRIP11):c.4069C>A (p.Gln1357Lys)
|
rs144829001
|
0.00101
|
NM_004239.4(TRIP11):c.1589G>A (p.Ser530Asn)
|
rs138304419
|
0.00093
|
NM_004239.4(TRIP11):c.5887G>A (p.Ala1963Thr)
|
rs61742059
|
0.00058
|
NM_004239.4(TRIP11):c.4620T>C (p.Val1540=)
|
rs72705400
|
0.00049
|
NM_004239.4(TRIP11):c.4139C>T (p.Thr1380Ile)
|
rs117748213
|
0.00042
|
NM_004239.4(TRIP11):c.5124C>T (p.Asn1708=)
|
rs143872244
|
0.00031
|
NM_004239.4(TRIP11):c.5657T>C (p.Met1886Thr)
|
rs143392370
|
0.00029
|
NM_004239.4(TRIP11):c.5900A>G (p.Asn1967Ser)
|
rs113605039
|
0.00024
|
NM_004239.4(TRIP11):c.950A>T (p.Asp317Val)
|
rs140416653
|
0.00023
|
NM_004239.4(TRIP11):c.1375G>A (p.Ala459Thr)
|
rs372171033
|
0.00021
|
NM_004239.4(TRIP11):c.3380C>T (p.Ala1127Val)
|
rs191280213
|
0.00019
|
NM_004239.4(TRIP11):c.5719+2T>C
|
rs199736345
|
0.00014
|
NM_004239.4(TRIP11):c.4159G>A (p.Glu1387Lys)
|
rs201607866
|
0.00004
|
NM_004239.4(TRIP11):c.1587C>T (p.Ile529=)
|
rs762961289
|
0.00003
|
NM_004239.4(TRIP11):c.3871G>A (p.Val1291Ile)
|
rs142078341
|
0.00003
|
NM_004239.4(TRIP11):c.460C>T (p.Pro154Ser)
|
rs201247031
|
0.00003
|
NM_004239.4(TRIP11):c.5446G>A (p.Glu1816Lys)
|
rs1456373630
|
0.00002
|
NM_004239.4(TRIP11):c.111G>A (p.Met37Ile)
|
rs902936427
|
0.00001
|
NM_004239.4(TRIP11):c.1240G>T (p.Ala414Ser)
|
rs761670358
|
0.00001
|
NM_004239.4(TRIP11):c.203A>T (p.Asn68Ile)
|
rs773364224
|
0.00001
|
NM_004239.4(TRIP11):c.332A>C (p.Lys111Thr)
|
rs770534000
|
0.00001
|
NM_004239.4(TRIP11):c.5645C>A (p.Ser1882Tyr)
|
rs371689436
|
0.00001
|
NM_004239.4(TRIP11):c.969T>G (p.Ser323=)
|
rs768358054
|
0.00001
|
NM_004239.4(TRIP11):c.2125A>G (p.Thr709Ala)
|
|
|
NM_004239.4(TRIP11):c.3817A>C (p.Ser1273Arg)
|
rs2140116644
|
|
NM_004239.4(TRIP11):c.4558-18A>C
|
rs201561387
|
|
NM_004239.4(TRIP11):c.4842A>G (p.Thr1614=)
|
|
|
NM_004239.4(TRIP11):c.5068A>G (p.Met1690Val)
|
rs542557164
|
|