ClinVar Miner

List of variants in gene combination RAD50, TH2LCRR reported as uncertain significance by Invitae

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Gene type:
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Total variants: 108
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HGVS dbSNP gnomAD frequency
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.3812A>G (p.Glu1271Gly) rs1237132499 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.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.3939A>T (p.Ter1313Tyr) rs121912629 0.00001
NM_005732.4(RAD50):c.3772C>G (p.Gln1258Glu) rs863224741
NM_005732.4(RAD50):c.3773A>G (p.Gln1258Arg) rs1751737904
NM_005732.4(RAD50):c.3776A>G (p.Gln1259Arg) rs1561661762
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.3781A>G (p.Asn1261Asp)
NM_005732.4(RAD50):c.3784T>G (p.Phe1262Val)
NM_005732.4(RAD50):c.3785T>G (p.Phe1262Cys) rs1751738874
NM_005732.4(RAD50):c.3791T>C (p.Leu1264Pro) rs1561661794
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.3797T>G (p.Val1266Gly) rs1060501971
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.3805C>G (p.His1269Asp) rs876659730
NM_005732.4(RAD50):c.3805C>T (p.His1269Tyr) rs876659730
NM_005732.4(RAD50):c.3807T>G (p.His1269Gln)
NM_005732.4(RAD50):c.3809A>T (p.Asp1270Val) rs1581025025
NM_005732.4(RAD50):c.3810_3840dup (p.Glu1281Ter)
NM_005732.4(RAD50):c.3811G>A (p.Glu1271Lys) rs1751740422
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.3830T>C (p.Leu1277Ser) rs1465553844
NM_005732.4(RAD50):c.3833G>A (p.Gly1278Glu)
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.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.3846del (p.Glu1281_Tyr1282insTer)
NM_005732.4(RAD50):c.3847G>A (p.Val1283Met) rs876659358
NM_005732.4(RAD50):c.3852_3855del (p.Glu1284fs) rs2149866975
NM_005732.4(RAD50):c.3855dup (p.Phe1286fs)
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.3860A>G (p.Tyr1287Cys) rs1751743134
NM_005732.4(RAD50):c.3863G>C (p.Arg1288Thr) 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.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.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.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.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>T (p.Glu1298Asp) rs1751745380
NM_005732.4(RAD50):c.3896T>C (p.Ile1299Thr) rs2149867058
NM_005732.4(RAD50):c.3898G>A (p.Val1300Met) rs1554101335
NM_005732.4(RAD50):c.3905G>A (p.Cys1302Tyr)
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.3909_3912dup (p.Ser1305delinsCysTer) rs1751745988
NM_005732.4(RAD50):c.3910G>A (p.Val1304Ile) rs1581025217
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.3919C>G (p.Leu1307Val)
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.3935A>C (p.His1312Pro) rs758732036

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