ClinVar Miner

List of variants in gene combination RAD50, TH2-LCR, TH2LCRR reported as likely benign for Hereditary cancer-predisposing syndrome

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Gene type:
ClinVar version:
Total variants: 164
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HGVS dbSNP gnomAD frequency
NM_005732.4(RAD50):c.3455G>A (p.Arg1152Gln) rs144253015 0.00025
NM_005732.4(RAD50):c.3508G>A (p.Asp1170Asn) rs397507179 0.00010
NM_005732.4(RAD50):c.3769T>G (p.Ser1257Ala) rs786201205 0.00008
NM_005732.4(RAD50):c.3456A>T (p.Arg1152=) rs775075281 0.00006
NM_005732.4(RAD50):c.3752+7A>G rs375301575 0.00006
NM_005732.4(RAD50):c.3496C>T (p.Arg1166Trp) rs587782577 0.00005
NM_005732.4(RAD50):c.3753-9T>C rs769773414 0.00004
NM_005732.4(RAD50):c.3476-16C>A rs577900904 0.00003
NM_005732.4(RAD50):c.3507C>T (p.Ala1169=) rs144557787 0.00003
NM_005732.4(RAD50):c.3752+7_3752+9dup rs772887509 0.00003
NM_005732.4(RAD50):c.3486C>T (p.Tyr1162=) rs864622078 0.00002
NM_005732.4(RAD50):c.3609T>G (p.Ala1203=) rs766082130 0.00002
NM_005732.4(RAD50):c.3642C>T (p.Arg1214=) rs752662569 0.00002
NM_005732.4(RAD50):c.3687C>T (p.Ala1229=) rs139099583 0.00002
NM_005732.4(RAD50):c.3696G>A (p.Glu1232=) rs749673167 0.00002
NM_005732.4(RAD50):c.3753-10A>G rs759837235 0.00002
NM_005732.4(RAD50):c.3753-18C>T rs777036298 0.00002
NM_005732.4(RAD50):c.3390-17A>G rs779048090 0.00001
NM_005732.4(RAD50):c.3390-20C>T rs755149427 0.00001
NM_005732.4(RAD50):c.3390-9C>T rs974787431 0.00001
NM_005732.4(RAD50):c.3444T>C (p.Arg1148=) rs1159262705 0.00001
NM_005732.4(RAD50):c.3466C>T (p.Arg1156Cys) rs535261113 0.00001
NM_005732.4(RAD50):c.3475+10A>C rs754465293 0.00001
NM_005732.4(RAD50):c.3475+13G>A rs755497258 0.00001
NM_005732.4(RAD50):c.3475+14T>C rs201741621 0.00001
NM_005732.4(RAD50):c.3476-12T>C rs771483160 0.00001
NM_005732.4(RAD50):c.3476-18T>C rs774186415 0.00001
NM_005732.4(RAD50):c.3497G>T (p.Arg1166Leu) rs763145238 0.00001
NM_005732.4(RAD50):c.3516T>C (p.Asn1172=) rs876659574 0.00001
NM_005732.4(RAD50):c.3522A>T (p.Ser1174=) rs750262906 0.00001
NM_005732.4(RAD50):c.3543T>C (p.Asn1181=) rs749147171 0.00001
NM_005732.4(RAD50):c.3546T>C (p.Tyr1182=) rs786201818 0.00001
NM_005732.4(RAD50):c.3561G>A (p.Val1187=) rs772962371 0.00001
NM_005732.4(RAD50):c.3579A>G (p.Thr1193=) rs1158993684 0.00001
NM_005732.4(RAD50):c.3619-10T>C rs766565530 0.00001
NM_005732.4(RAD50):c.3619-11C>T rs974991715 0.00001
NM_005732.4(RAD50):c.3619-15G>A rs773550133 0.00001
NM_005732.4(RAD50):c.3619-17T>C rs767553753 0.00001
NM_005732.4(RAD50):c.3619-18A>G rs761928936 0.00001
NM_005732.4(RAD50):c.3621A>G (p.Val1207=) rs786201767 0.00001
NM_005732.4(RAD50):c.3648C>T (p.Ala1216=) rs1554101176 0.00001
NM_005732.4(RAD50):c.3660G>A (p.Thr1220=) rs758026288 0.00001
NM_005732.4(RAD50):c.3669C>G (p.Leu1223=) rs200496768 0.00001
NM_005732.4(RAD50):c.3752+17C>T rs1350488185 0.00001
NM_005732.4(RAD50):c.3752+20G>C rs992571236 0.00001
NM_005732.4(RAD50):c.3752+3A>G rs864622704 0.00001
NM_005732.4(RAD50):c.3752+9C>T rs765096225 0.00001
NM_005732.4(RAD50):c.3753-20T>G rs771024744 0.00001
NM_005732.4(RAD50):c.3753-4G>T rs775426160 0.00001
NM_005732.4(RAD50):c.3390-10C>T rs1751595393
NM_005732.4(RAD50):c.3390-20C>G rs755149427
NM_005732.4(RAD50):c.3390-4C>T rs1436912972
NM_005732.4(RAD50):c.3390-5T>C rs1561658734
NM_005732.4(RAD50):c.3402A>G (p.Lys1134=) rs876658778
NM_005732.4(RAD50):c.3405T>C (p.Phe1135=) rs1554100854
NM_005732.4(RAD50):c.3408C>T (p.His1136=) rs786201225
NM_005732.4(RAD50):c.3417A>G (p.Lys1139=)
NM_005732.4(RAD50):c.3426A>G (p.Glu1142=) rs1554100860
NM_005732.4(RAD50):c.3429C>A (p.Ile1143=) rs1581020189
NM_005732.4(RAD50):c.3438T>A (p.Ile1146=)
NM_005732.4(RAD50):c.3438T>C (p.Ile1146=) rs777795463
NM_005732.4(RAD50):c.3447C>T (p.Asp1149=) rs876658882
NM_005732.4(RAD50):c.3448C>T (p.Leu1150=) rs2149862762
NM_005732.4(RAD50):c.3450G>C (p.Leu1150=)
NM_005732.4(RAD50):c.3459T>C (p.Ser1153=)
NM_005732.4(RAD50):c.3462C>A (p.Thr1154=) rs958083506
NM_005732.4(RAD50):c.3462C>T (p.Thr1154=) rs958083506
NM_005732.4(RAD50):c.3468T>G (p.Arg1156=) rs1056543818
NM_005732.4(RAD50):c.3475+10A>G rs754465293
NM_005732.4(RAD50):c.3475+11T>C
NM_005732.4(RAD50):c.3475+12G>A rs2149862838
NM_005732.4(RAD50):c.3475+12G>C
NM_005732.4(RAD50):c.3475+13G>T rs755497258
NM_005732.4(RAD50):c.3475+15G>A rs2149862844
NM_005732.4(RAD50):c.3475+5G>C rs1288724170
NM_005732.4(RAD50):c.3475+7A>T rs1308559313
NM_005732.4(RAD50):c.3475+8C>T rs766820555
NM_005732.4(RAD50):c.3475+9dup rs2149862832
NM_005732.4(RAD50):c.3476-10C>A rs2149863417
NM_005732.4(RAD50):c.3476-10C>T
NM_005732.4(RAD50):c.3476-12T>G
NM_005732.4(RAD50):c.3476-15T>C rs2149863410
NM_005732.4(RAD50):c.3476-17T>C
NM_005732.4(RAD50):c.3476-18T>G
NM_005732.4(RAD50):c.3476-18TTC[2] rs730881922
NM_005732.4(RAD50):c.3476-7G>A rs1283810116
NM_005732.4(RAD50):c.3476-8T>G rs2149863419
NM_005732.4(RAD50):c.3476-9C>A
NM_005732.4(RAD50):c.3476-9C>T rs1448951364
NM_005732.4(RAD50):c.3483A>G (p.Glu1161=) rs777148895
NM_005732.4(RAD50):c.3498G>T (p.Arg1166=)
NM_005732.4(RAD50):c.3510T>C (p.Asp1170=)
NM_005732.4(RAD50):c.3519A>G (p.Val1173=) rs781320722
NM_005732.4(RAD50):c.3522A>G (p.Ser1174=) rs750262906
NM_005732.4(RAD50):c.3528T>C (p.Ser1176=)
NM_005732.4(RAD50):c.3528T>G (p.Ser1176=)
NM_005732.4(RAD50):c.3531T>C (p.Asp1177=) rs1415093880
NM_005732.4(RAD50):c.3537G>A (p.Arg1179=) rs2149863555
NM_005732.4(RAD50):c.3538C>A (p.Arg1180=)
NM_005732.4(RAD50):c.3558G>A (p.Val1186=)
NM_005732.4(RAD50):c.3558G>C (p.Val1186=) rs2149863600
NM_005732.4(RAD50):c.3567G>A (p.Leu1189=) rs759971562
NM_005732.4(RAD50):c.3582C>T (p.Ala1194=)
NM_005732.4(RAD50):c.3583T>C (p.Leu1195=)
NM_005732.4(RAD50):c.3585G>A (p.Leu1195=) rs786201774
NM_005732.4(RAD50):c.3598C>A (p.Arg1200=) rs750586158
NM_005732.4(RAD50):c.3600A>T (p.Arg1200=) rs1241453759
NM_005732.4(RAD50):c.3603C>T (p.Cys1201=) rs925410997
NM_005732.4(RAD50):c.3618+10T>G
NM_005732.4(RAD50):c.3618+10_3618+11del rs2149863712
NM_005732.4(RAD50):c.3618+11C>G
NM_005732.4(RAD50):c.3618+12_3618+17del
NM_005732.4(RAD50):c.3618+17C>G rs1233183992
NM_005732.4(RAD50):c.3618+17C>T rs1233183992
NM_005732.4(RAD50):c.3618+19_3618+32delinsAGTT rs2149863726
NM_005732.4(RAD50):c.3618+20G>A
NM_005732.4(RAD50):c.3618+7A>G rs1060504399
NM_005732.4(RAD50):c.3618+9C>T rs2149863713
NM_005732.4(RAD50):c.3619-10T>G rs766565530
NM_005732.4(RAD50):c.3619-12G>A rs760795345
NM_005732.4(RAD50):c.3619-13G>A rs2149865487
NM_005732.4(RAD50):c.3619-15G>C
NM_005732.4(RAD50):c.3619-16_3619-15del
NM_005732.4(RAD50):c.3619-5dup rs1411469588
NM_005732.4(RAD50):c.3627C>T (p.Ala1209=) rs2149865539
NM_005732.4(RAD50):c.3630A>G (p.Ser1210=) rs1301826986
NM_005732.4(RAD50):c.3633C>A (p.Leu1211=)
NM_005732.4(RAD50):c.3633C>G (p.Leu1211=) rs876660945
NM_005732.4(RAD50):c.3633C>T (p.Leu1211=) rs876660945
NM_005732.4(RAD50):c.3645G>A (p.Leu1215=)
NM_005732.4(RAD50):c.3648C>A (p.Ala1216=) rs1554101176
NM_005732.4(RAD50):c.3648C>G (p.Ala1216=)
NM_005732.4(RAD50):c.3651G>C (p.Leu1217=) rs1554101178
NM_005732.4(RAD50):c.3654T>A (p.Ala1218=)
NM_005732.4(RAD50):c.3654T>C (p.Ala1218=) rs2149865610
NM_005732.4(RAD50):c.3660G>C (p.Thr1220=)
NM_005732.4(RAD50):c.3660G>T (p.Thr1220=) rs758026288
NM_005732.4(RAD50):c.3663C>T (p.Phe1221=)
NM_005732.4(RAD50):c.3672C>T (p.Asn1224=) rs1220065101
NM_005732.4(RAD50):c.3675T>C (p.Cys1225=)
NM_005732.4(RAD50):c.3687C>G (p.Ala1229=) rs139099583
NM_005732.4(RAD50):c.3690G>A (p.Leu1230=) rs1561660969
NM_005732.4(RAD50):c.3726T>C (p.Ile1242=)
NM_005732.4(RAD50):c.3732T>C (p.Ser1244=) rs2149865829
NM_005732.4(RAD50):c.3735T>A (p.Leu1245=) rs531780578
NM_005732.4(RAD50):c.3738A>C (p.Ala1246=) rs1581023849
NM_005732.4(RAD50):c.3741T>C (p.His1247=) rs2149865854
NM_005732.4(RAD50):c.3744T>C (p.Ala1248=) rs1554101204
NM_005732.4(RAD50):c.3745C>T (p.Leu1249=) rs1230753352
NM_005732.4(RAD50):c.3752+12_3752+41del
NM_005732.4(RAD50):c.3752+14_3752+43del
NM_005732.4(RAD50):c.3752+18A>C
NM_005732.4(RAD50):c.3752+8T>C rs367888587
NM_005732.4(RAD50):c.3752+8T>G rs367888587
NM_005732.4(RAD50):c.3752+9C>G rs765096225
NM_005732.4(RAD50):c.3753-16G>T
NM_005732.4(RAD50):c.3753-17del rs2149866781
NM_005732.4(RAD50):c.3753-18C>G rs777036298
NM_005732.4(RAD50):c.3753-19T>G rs1217569216
NM_005732.4(RAD50):c.3753-6_3753-4del rs2149866791
NM_005732.4(RAD50):c.3753-7G>T rs2149866795
NM_005732.4(RAD50):c.3753G>A (p.Glu1251=) rs762792547
NM_005732.4(RAD50):c.3756A>C (p.Ile1252=) rs763958218
NM_005732.4(RAD50):c.3765T>C (p.Ser1255=) rs1554101316

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