NM_005732.4(RAD50):c.3836G>A (p.Arg1279His)
|
rs375710541
|
0.00007
|
NM_005732.4(RAD50):c.3880G>A (p.Asp1294Asn)
|
rs587782339
|
0.00005
|
NM_005732.4(RAD50):c.3877A>G (p.Ile1293Val)
|
rs762702502
|
0.00003
|
NM_005732.4(RAD50):c.3789G>C (p.Gln1263His)
|
rs115706334
|
0.00002
|
NM_005732.4(RAD50):c.3779G>A (p.Arg1260His)
|
rs367683141
|
0.00001
|
NM_005732.4(RAD50):c.3824A>G (p.Glu1275Gly)
|
rs372924978
|
0.00001
|
NM_005732.4(RAD50):c.3835C>T (p.Arg1279Cys)
|
rs786201810
|
0.00001
|
NM_005732.4(RAD50):c.3839C>G (p.Ser1280Cys)
|
rs747522239
|
0.00001
|
NM_005732.4(RAD50):c.3882T>G (p.Asp1294Glu)
|
rs587781426
|
0.00001
|
NM_005732.4(RAD50):c.3884A>G (p.Gln1295Arg)
|
rs1045257429
|
0.00001
|
NM_005732.4(RAD50):c.3929A>G (p.Asn1310Ser)
|
rs753468016
|
0.00001
|
NM_005732.4(RAD50):c.3931G>A (p.Val1311Ile)
|
rs863224743
|
0.00001
|
NM_005732.4(RAD50):c.3935A>G (p.His1312Arg)
|
rs758732036
|
0.00001
|
NM_005732.4(RAD50):c.3772C>G (p.Gln1258Glu)
|
rs863224741
|
|
NM_005732.4(RAD50):c.3777G>T (p.Gln1259His)
|
rs587780157
|
|
NM_005732.4(RAD50):c.3782A>G (p.Asn1261Ser)
|
|
|
NM_005732.4(RAD50):c.3784_3786dup (p.Phe1262_Gln1263insPhe)
|
|
|
NM_005732.4(RAD50):c.3786C>G (p.Phe1262Leu)
|
rs267600344
|
|
NM_005732.4(RAD50):c.3791T>C (p.Leu1264Pro)
|
rs1561661794
|
|
NM_005732.4(RAD50):c.3793C>G (p.Leu1265Val)
|
|
|
NM_005732.4(RAD50):c.3796G>A (p.Val1266Ile)
|
rs750133404
|
|
NM_005732.4(RAD50):c.3796G>C (p.Val1266Leu)
|
|
|
NM_005732.4(RAD50):c.3796_3809dup (p.Asp1270delinsGluTer)
|
|
|
NM_005732.4(RAD50):c.3799A>C (p.Ile1267Leu)
|
|
|
NM_005732.4(RAD50):c.3799A>G (p.Ile1267Val)
|
rs1751739783
|
|
NM_005732.4(RAD50):c.3799dup (p.Ile1267fs)
|
rs1554101324
|
|
NM_005732.4(RAD50):c.3800T>A (p.Ile1267Asn)
|
rs1581025004
|
|
NM_005732.4(RAD50):c.3805C>T (p.His1269Tyr)
|
rs876659730
|
|
NM_005732.4(RAD50):c.3806A>C (p.His1269Pro)
|
|
|
NM_005732.4(RAD50):c.3806_3807del (p.His1269fs)
|
rs1085307088
|
|
NM_005732.4(RAD50):c.3807T>G (p.His1269Gln)
|
|
|
NM_005732.4(RAD50):c.3809A>T (p.Asp1270Val)
|
rs1581025025
|
|
NM_005732.4(RAD50):c.3810T>A (p.Asp1270Glu)
|
|
|
NM_005732.4(RAD50):c.3811G>A (p.Glu1271Lys)
|
rs1751740422
|
|
NM_005732.4(RAD50):c.3813A>T (p.Glu1271Asp)
|
|
|
NM_005732.4(RAD50):c.3813_3815del (p.Glu1271del)
|
rs776601293
|
|
NM_005732.4(RAD50):c.3814G>C (p.Asp1272His)
|
rs753091579
|
|
NM_005732.4(RAD50):c.3816T>G (p.Asp1272Glu)
|
rs1581025045
|
|
NM_005732.4(RAD50):c.3817T>G (p.Phe1273Val)
|
rs2149866931
|
|
NM_005732.4(RAD50):c.3818T>C (p.Phe1273Ser)
|
|
|
NM_005732.4(RAD50):c.3826C>T (p.Leu1276Phe)
|
|
|
NM_005732.4(RAD50):c.3827T>G (p.Leu1276Arg)
|
|
|
NM_005732.4(RAD50):c.3836G>T (p.Arg1279Leu)
|
rs375710541
|
|
NM_005732.4(RAD50):c.3839del (p.Ser1280fs)
|
|
|
NM_005732.4(RAD50):c.3841_3859del (p.Glu1281fs)
|
rs1561661862
|
|
NM_005732.4(RAD50):c.3842A>C (p.Glu1281Ala)
|
rs863224742
|
|
NM_005732.4(RAD50):c.3844T>A (p.Tyr1282Asn)
|
rs587782219
|
|
NM_005732.4(RAD50):c.3847G>A (p.Val1283Met)
|
rs876659358
|
|
NM_005732.4(RAD50):c.3857T>A (p.Phe1286Tyr)
|
rs587781369
|
|
NM_005732.4(RAD50):c.3857T>C (p.Phe1286Ser)
|
rs587781369
|
|
NM_005732.4(RAD50):c.3857T>G (p.Phe1286Cys)
|
rs587781369
|
|
NM_005732.4(RAD50):c.3858C>A (p.Phe1286Leu)
|
rs1581025102
|
|
NM_005732.4(RAD50):c.3863G>C (p.Arg1288Thr)
|
rs202098299
|
|
NM_005732.4(RAD50):c.3863G>T (p.Arg1288Met)
|
rs202098299
|
|
NM_005732.4(RAD50):c.3865A>T (p.Ile1289Phe)
|
rs1751743610
|
|
NM_005732.4(RAD50):c.3866T>A (p.Ile1289Asn)
|
rs1554101330
|
|
NM_005732.4(RAD50):c.3872_3893del (p.Lys1291fs)
|
rs759582800
|
|
NM_005732.4(RAD50):c.3874A>G (p.Asn1292Asp)
|
rs1554101333
|
|
NM_005732.4(RAD50):c.3877A>T (p.Ile1293Phe)
|
rs762702502
|
|
NM_005732.4(RAD50):c.3883C>T (p.Gln1295Ter)
|
rs1330031894
|
|
NM_005732.4(RAD50):c.3894G>T (p.Glu1298Asp)
|
rs1751745380
|
|
NM_005732.4(RAD50):c.3895A>G (p.Ile1299Val)
|
|
|
NM_005732.4(RAD50):c.3898G>A (p.Val1300Met)
|
rs1554101335
|
|
NM_005732.4(RAD50):c.3907A>G (p.Ser1303Gly)
|
rs876659120
|
|
NM_005732.4(RAD50):c.3908G>C (p.Ser1303Thr)
|
rs766044158
|
|
NM_005732.4(RAD50):c.3910G>A (p.Val1304Ile)
|
rs1581025217
|
|
NM_005732.4(RAD50):c.3922G>A (p.Gly1308Arg)
|
|
|
NM_005732.4(RAD50):c.3929A>C (p.Asn1310Thr)
|
rs753468016
|
|