ClinVar Miner

List of variants in gene RAD50, TH2LCRR studied for Hereditary cancer-predisposing syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 178
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_005732.4(RAD50):c.3846T>C (p.Tyr1282=) rs1804670 0.05209
NM_005732.4(RAD50):c.3879C>T (p.Ile1293=) rs28903094 0.00293
NM_005732.4(RAD50):c.3861C>T (p.Tyr1287=) rs368356436 0.00019
NM_005732.4(RAD50):c.3790C>T (p.Leu1264Phe) rs199579239 0.00009
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.3778C>T (p.Arg1260Cys) rs1381323366 0.00001
NM_005732.4(RAD50):c.3779G>A (p.Arg1260His) rs367683141 0.00001
NM_005732.4(RAD50):c.3807T>C (p.His1269=) rs755777007 0.00001
NM_005732.4(RAD50):c.3812A>G (p.Glu1271Gly) rs1237132499 0.00001
NM_005732.4(RAD50):c.3813A>G (p.Glu1271=) rs1302002047 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.3869A>C (p.Lys1290Thr) rs1156612738 0.00001
NM_005732.4(RAD50):c.3876C>T (p.Asn1292=) rs1300783013 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.3897T>A (p.Ile1299=) rs767384027 0.00001
NM_005732.4(RAD50):c.3902A>G (p.Lys1301Arg) rs201766077 0.00001
NM_005732.4(RAD50):c.3915C>T (p.Ser1305=) rs1183659259 0.00001
NM_005732.4(RAD50):c.3929A>G (p.Asn1310Ser) rs753468016 0.00001
NM_005732.4(RAD50):c.3930T>C (p.Asn1310=) rs878854803 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.3939A>T (p.Ter1313Tyr) rs121912629 0.00001
NM_005732.4(RAD50):c.3772C>G (p.Gln1258Glu) rs863224741
NM_005732.4(RAD50):c.3772C>T (p.Gln1258Ter) rs863224741
NM_005732.4(RAD50):c.3773A>G (p.Gln1258Arg) rs1751737904
NM_005732.4(RAD50):c.3774G>A (p.Gln1258=) rs1060504404
NM_005732.4(RAD50):c.3775_3788del (p.Gln1259fs) rs1581024929
NM_005732.4(RAD50):c.3776A>G (p.Gln1259Arg) rs1561661762
NM_005732.4(RAD50):c.3777G>A (p.Gln1259=) rs587780157
NM_005732.4(RAD50):c.3777G>T (p.Gln1259His) rs587780157
NM_005732.4(RAD50):c.3779G>C (p.Arg1260Pro) rs367683141
NM_005732.4(RAD50):c.3779G>T (p.Arg1260Leu) rs367683141
NM_005732.4(RAD50):c.3779_3791dup (p.Leu1264_Leu1265insTer) rs1561661777
NM_005732.4(RAD50):c.3779del (p.Arg1260fs) rs786202259
NM_005732.4(RAD50):c.3780dup (p.Asn1261Ter) rs1581024951
NM_005732.4(RAD50):c.3781A>G (p.Asn1261Asp)
NM_005732.4(RAD50):c.3781_3784dup (p.Phe1262Ter) rs1581024954
NM_005732.4(RAD50):c.3782A>G (p.Asn1261Ser)
NM_005732.4(RAD50):c.3783C>T (p.Asn1261=) rs1581024957
NM_005732.4(RAD50):c.3784T>G (p.Phe1262Val)
NM_005732.4(RAD50):c.3784_3786dup (p.Phe1262_Gln1263insPhe)
NM_005732.4(RAD50):c.3785T>G (p.Phe1262Cys) rs1751738874
NM_005732.4(RAD50):c.3786C>G (p.Phe1262Leu) rs267600344
NM_005732.4(RAD50):c.3786C>T (p.Phe1262=) rs267600344
NM_005732.4(RAD50):c.3786_3787delinsTT (p.Gln1263Ter) rs2149866877
NM_005732.4(RAD50):c.3787C>T (p.Gln1263Ter) rs876659654
NM_005732.4(RAD50):c.3789G>A (p.Gln1263=) rs115706334
NM_005732.4(RAD50):c.3791T>C (p.Leu1264Pro) rs1561661794
NM_005732.4(RAD50):c.3792T>A (p.Leu1264=) rs2149866888
NM_005732.4(RAD50):c.3793C>G (p.Leu1265Val)
NM_005732.4(RAD50):c.3794T>C (p.Leu1265Pro) rs2149866892
NM_005732.4(RAD50):c.3795_3815dup (p.Glu1271_Asp1272insGluValIleThrHisAspGlu) rs2149866895
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.3797T>G (p.Val1266Gly) rs1060501971
NM_005732.4(RAD50):c.3798A>G (p.Val1266=)
NM_005732.4(RAD50):c.3799A>C (p.Ile1267Leu)
NM_005732.4(RAD50):c.3799A>G (p.Ile1267Val) rs1751739783
NM_005732.4(RAD50):c.3799_3802dup (p.Thr1268fs) rs766326955
NM_005732.4(RAD50):c.3799dup (p.Ile1267fs) rs1554101324
NM_005732.4(RAD50):c.3800T>A (p.Ile1267Asn) rs1581025004
NM_005732.4(RAD50):c.3801C>T (p.Ile1267=) rs1554101325
NM_005732.4(RAD50):c.3805C>G (p.His1269Asp) rs876659730
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.3810T>C (p.Asp1270=) rs1486093198
NM_005732.4(RAD50):c.3810_3840dup (p.Glu1281Ter)
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.3814G>T (p.Asp1272Tyr) 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.3819dup (p.Val1274fs) rs1751740888
NM_005732.4(RAD50):c.3820G>A (p.Val1274Met) rs1060501978
NM_005732.4(RAD50):c.3826C>T (p.Leu1276Phe)
NM_005732.4(RAD50):c.3827T>G (p.Leu1276Arg)
NM_005732.4(RAD50):c.3830T>C (p.Leu1277Ser) rs1465553844
NM_005732.4(RAD50):c.3833G>A (p.Gly1278Glu)
NM_005732.4(RAD50):c.3834A>G (p.Gly1278=)
NM_005732.4(RAD50):c.3835C>G (p.Arg1279Gly) rs786201810
NM_005732.4(RAD50):c.3836G>T (p.Arg1279Leu) rs375710541
NM_005732.4(RAD50):c.3838T>C (p.Ser1280Pro) rs1751741883
NM_005732.4(RAD50):c.3839del (p.Ser1280fs)
NM_005732.4(RAD50):c.3840T>C (p.Ser1280=)
NM_005732.4(RAD50):c.3841G>T (p.Glu1281Ter) rs781413356
NM_005732.4(RAD50):c.3841_3857del (p.Glu1281fs)
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.3843A>G (p.Glu1281=) rs1581025084
NM_005732.4(RAD50):c.3844T>A (p.Tyr1282Asn) rs587782219
NM_005732.4(RAD50):c.3846del (p.Glu1281_Tyr1282insTer)
NM_005732.4(RAD50):c.3847G>A (p.Val1283Met) rs876659358
NM_005732.4(RAD50):c.3849G>A (p.Val1283=) rs1160803447
NM_005732.4(RAD50):c.3852_3855del (p.Glu1284fs) rs2149866975
NM_005732.4(RAD50):c.3855A>G (p.Lys1285=) rs1581025096
NM_005732.4(RAD50):c.3855dup (p.Phe1286fs)
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.3858C>T (p.Phe1286=) rs1581025102
NM_005732.4(RAD50):c.3860A>G (p.Tyr1287Cys) rs1751743134
NM_005732.4(RAD50):c.3862A>C (p.Arg1288=)
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.3864G>C (p.Arg1288Ser) rs775802277
NM_005732.4(RAD50):c.3864del (p.Ile1289fs) rs1581025119
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.3866T>C (p.Ile1289Thr) rs1554101330
NM_005732.4(RAD50):c.3868A>G (p.Lys1290Glu)
NM_005732.4(RAD50):c.3868A>T (p.Lys1290Ter) rs2149866998
NM_005732.4(RAD50):c.3872_3893del (p.Lys1291fs) rs759582800
NM_005732.4(RAD50):c.3872del (p.Lys1291fs)
NM_005732.4(RAD50):c.3872dup (p.Asn1292fs) rs1581025123
NM_005732.4(RAD50):c.3873G>A (p.Lys1291=) rs2149867004
NM_005732.4(RAD50):c.3873_3875del (p.Lys1291del)
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.3877_3879dup (p.Ile1293dup) rs765370709
NM_005732.4(RAD50):c.3880G>C (p.Asp1294His)
NM_005732.4(RAD50):c.3880_3881insT (p.Asp1294fs)
NM_005732.4(RAD50):c.3883C>T (p.Gln1295Ter) rs1330031894
NM_005732.4(RAD50):c.3885G>T (p.Gln1295His) rs1561661938
NM_005732.4(RAD50):c.3886T>A (p.Cys1296Ser) rs1223441991
NM_005732.4(RAD50):c.3886T>C (p.Cys1296Arg)
NM_005732.4(RAD50):c.3888C>T (p.Cys1296=) rs1581025172
NM_005732.4(RAD50):c.3889T>C (p.Ser1297Pro) rs905344109
NM_005732.4(RAD50):c.3890C>A (p.Ser1297Ter) rs2149867051
NM_005732.4(RAD50):c.3890C>G (p.Ser1297Ter)
NM_005732.4(RAD50):c.3891A>C (p.Ser1297=) rs2149867053
NM_005732.4(RAD50):c.3891A>G (p.Ser1297=) rs2149867053
NM_005732.4(RAD50):c.3892G>A (p.Glu1298Lys) rs1422137796
NM_005732.4(RAD50):c.3892G>C (p.Glu1298Gln) rs1422137796
NM_005732.4(RAD50):c.3893A>G (p.Glu1298Gly) rs1581025186
NM_005732.4(RAD50):c.3894G>A (p.Glu1298=) rs1751745380
NM_005732.4(RAD50):c.3894G>T (p.Glu1298Asp) rs1751745380
NM_005732.4(RAD50):c.3896T>C (p.Ile1299Thr) rs2149867058
NM_005732.4(RAD50):c.3897T>C (p.Ile1299=) rs767384027
NM_005732.4(RAD50):c.3898G>A (p.Val1300Met) rs1554101335
NM_005732.4(RAD50):c.3900G>A (p.Val1300=) rs2149867065
NM_005732.4(RAD50):c.3905G>A (p.Cys1302Tyr)
NM_005732.4(RAD50):c.3906C>T (p.Cys1302=) rs2149867072
NM_005732.4(RAD50):c.3907A>G (p.Ser1303Gly) rs876659120
NM_005732.4(RAD50):c.3908G>A (p.Ser1303Asn) rs766044158
NM_005732.4(RAD50):c.3908G>C (p.Ser1303Thr) rs766044158
NM_005732.4(RAD50):c.3908G>T (p.Ser1303Ile) rs766044158
NM_005732.4(RAD50):c.3909T>C (p.Ser1303=) rs2149867080
NM_005732.4(RAD50):c.3909_3912dup (p.Ser1305delinsCysTer) rs1751745988
NM_005732.4(RAD50):c.3910G>A (p.Val1304Ile) rs1581025217
NM_005732.4(RAD50):c.3912T>C (p.Val1304=)
NM_005732.4(RAD50):c.3914G>C (p.Ser1305Thr)
NM_005732.4(RAD50):c.3916T>C (p.Ser1306Pro) rs1751746223
NM_005732.4(RAD50):c.3916del (p.Ser1306fs) rs1561661957
NM_005732.4(RAD50):c.3918C>G (p.Ser1306=) rs1554101337
NM_005732.4(RAD50):c.3919C>G (p.Leu1307Val)
NM_005732.4(RAD50):c.3921G>C (p.Leu1307=) rs1554101338
NM_005732.4(RAD50):c.3922G>A (p.Gly1308Arg)
NM_005732.4(RAD50):c.3928A>G (p.Asn1310Asp) rs1581025242
NM_005732.4(RAD50):c.3929A>C (p.Asn1310Thr) rs753468016
NM_005732.4(RAD50):c.3930T>A (p.Asn1310Lys)
NM_005732.4(RAD50):c.3933T>C (p.Val1311=) rs876660513
NM_005732.4(RAD50):c.3935A>C (p.His1312Pro) rs758732036
NM_005732.4(RAD50):c.3938_*30dup (p.Ter1313=) rs2149867108

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.