ClinVar Miner

List of variants in gene RAD50 reported as likely benign for not provided

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 100
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HGVS dbSNP
NM_005732.4(RAD50):c.1005A>G (p.Glu335=) rs747098394
NM_005732.4(RAD50):c.1017C>T (p.Leu339=) rs1580992305
NM_005732.4(RAD50):c.1032A>G (p.Ser344=) rs1060504400
NM_005732.4(RAD50):c.1041T>C (p.Leu347=) rs1580992351
NM_005732.4(RAD50):c.1051+9A>T rs1580992371
NM_005732.4(RAD50):c.1131G>A (p.Gln377=) rs786202849
NM_005732.4(RAD50):c.1179T>A (p.Ile393=) rs1580992858
NM_005732.4(RAD50):c.1207A>C (p.Arg403=) rs201461054
NM_005732.4(RAD50):c.1242G>A (p.Leu414=) rs1554098273
NM_005732.4(RAD50):c.1246-8G>T rs776650264
NM_005732.4(RAD50):c.1269T>G (p.Thr423=) rs745374544
NM_005732.4(RAD50):c.126G>A (p.Lys42=) rs754823399
NM_005732.4(RAD50):c.1275A>G (p.Lys425=) rs769385714
NM_005732.4(RAD50):c.1278A>G (p.Gln426=) rs1580993375
NM_005732.4(RAD50):c.129+10C>T rs570876192
NM_005732.4(RAD50):c.130-8T>G rs1580976151
NM_005732.4(RAD50):c.1308A>G (p.Lys436=) rs1580993423
NM_005732.4(RAD50):c.1314A>T (p.Gly438=) rs755193751
NM_005732.4(RAD50):c.1356G>A (p.Lys452=) rs752912370
NM_005732.4(RAD50):c.135C>T (p.Ile45=) rs745566783
NM_005732.4(RAD50):c.1365T>C (p.Asn455=) rs1580993494
NM_005732.4(RAD50):c.1417A>C (p.Arg473=) rs1217523555
NM_005732.4(RAD50):c.141A>G (p.Glu47=) rs1257141008
NM_005732.4(RAD50):c.1428A>G (p.Glu476=) rs766691332
NM_005732.4(RAD50):c.1453-6G>A rs1580994303
NM_005732.4(RAD50):c.1482C>T (p.Asn494=) rs1360925930
NM_005732.4(RAD50):c.1488T>C (p.Asn496=) rs760093523
NM_005732.4(RAD50):c.1497C>G (p.Thr499=) rs1023524138
NM_005732.4(RAD50):c.1497C>T (p.Thr499=) rs1023524138
NM_005732.4(RAD50):c.1527T>C (p.Asn509=) rs863224408
NM_005732.4(RAD50):c.1530A>G (p.Glu510=) rs1060504396
NM_005732.4(RAD50):c.1536A>G (p.Ala512=) rs1580994374
NM_005732.4(RAD50):c.1552C>T (p.Leu518=) rs755918415
NM_005732.4(RAD50):c.1692C>A (p.Thr564=) rs876660850
NM_005732.4(RAD50):c.1773G>A (p.Arg591=) rs1561641146
NM_005732.4(RAD50):c.1777A>C (p.Arg593=) rs762842543
NM_005732.4(RAD50):c.1794-8del rs1060504394
NM_005732.4(RAD50):c.1794-9T>C rs1060504397
NM_005732.4(RAD50):c.1824A>G (p.Lys608=) rs1580996406
NM_005732.4(RAD50):c.1839T>C (p.Asn613=) rs1316773244
NM_005732.4(RAD50):c.1989A>G (p.Thr663=) rs863224409
NM_005732.4(RAD50):c.2043C>T (p.Cys681=) rs1580997003
NM_005732.4(RAD50):c.2106G>A (p.Gln702=) rs745384449
NM_005732.4(RAD50):c.213+7G>A rs1256911472
NM_005732.4(RAD50):c.2157A>G (p.Leu719=) rs876660158
NM_005732.4(RAD50):c.2208-9_2208-7del rs1465205983
NM_005732.4(RAD50):c.2244A>G (p.Pro748=) rs1424119975
NM_005732.4(RAD50):c.2248T>C (p.Leu750=) rs1554099085
NM_005732.4(RAD50):c.2289C>G (p.Arg763=) rs757669763
NM_005732.4(RAD50):c.2319A>G (p.Thr773=) rs1581001094
NM_005732.4(RAD50):c.2322C>G (p.Leu774=) rs1581001098
NM_005732.4(RAD50):c.2379A>G (p.Thr793=) rs1060504395
NM_005732.4(RAD50):c.2439A>G (p.Ala813=) rs1581001464
NM_005732.4(RAD50):c.2505A>G (p.Lys835=) rs996373843
NM_005732.4(RAD50):c.252G>A (p.Leu84=) rs1580985000
NM_005732.4(RAD50):c.2535G>A (p.Lys845=) rs1581002006
NM_005732.4(RAD50):c.2592A>G (p.Lys864=) rs1554099191
NM_005732.4(RAD50):c.2607G>A (p.Glu869=) rs876660389
NM_005732.4(RAD50):c.270T>C (p.Asn90=) rs1580985045
NM_005732.4(RAD50):c.2712G>A (p.Glu904=) rs1060504386
NM_005732.4(RAD50):c.2718+7A>C rs1581002263
NM_005732.4(RAD50):c.2719-4T>A rs1474922117
NM_005732.4(RAD50):c.2745G>A (p.Leu915=) rs876658662
NM_005732.4(RAD50):c.2811C>T (p.Asn937=) rs1554099325
NM_005732.4(RAD50):c.2814A>G (p.Lys938=) rs1581004311
NM_005732.4(RAD50):c.2838T>C (p.Asp946=) rs1581004591
NM_005732.4(RAD50):c.2892T>C (p.Tyr964=) rs780942620
NM_005732.4(RAD50):c.2949A>G (p.Val983=) rs371257256
NM_005732.4(RAD50):c.2976A>G (p.Lys992=) rs1581004895
NM_005732.4(RAD50):c.2979C>T (p.His993=) rs1060504403
NM_005732.4(RAD50):c.3030A>G (p.Thr1010=) rs771112938
NM_005732.4(RAD50):c.3046A>C (p.Arg1016=) rs1220686754
NM_005732.4(RAD50):c.3177G>A (p.Lys1059=) rs786202762
NM_005732.4(RAD50):c.3198T>C (p.Asn1066=) rs1581009384
NM_005732.4(RAD50):c.3294G>A (p.Arg1098=) rs1349921805
NM_005732.4(RAD50):c.3381T>C (p.Thr1127=) rs1372921882
NM_005732.4(RAD50):c.3381T>G (p.Thr1127=) rs1372921882
NM_005732.4(RAD50):c.3384T>A (p.Leu1128=) rs1060504387
NM_005732.4(RAD50):c.3389+8T>C rs1581009628
NM_005732.4(RAD50):c.351C>T (p.Val117=) rs878854800
NM_005732.4(RAD50):c.365+7G>A rs1554097580
NM_005732.4(RAD50):c.36G>A (p.Val12=) rs1580974379
NM_005732.4(RAD50):c.414A>C (p.Arg138=) rs1060504388
NM_005732.4(RAD50):c.528T>C (p.Phe176=) rs1379723744
NM_005732.4(RAD50):c.54G>A (p.Glu18=) rs1554096636
NM_005732.4(RAD50):c.555C>T (p.Tyr185=) rs1285412752
NM_005732.4(RAD50):c.567A>G (p.Leu189=) rs1554097800
NM_005732.4(RAD50):c.570A>G (p.Glu190=) rs1580987582
NM_005732.4(RAD50):c.572C>T (p.Thr191Ile) rs2230017
NM_005732.4(RAD50):c.756+8G>T rs751656699
NM_005732.4(RAD50):c.757-4T>C rs1554098154
NM_005732.4(RAD50):c.757-7T>A rs1580991770
NM_005732.4(RAD50):c.757-8A>G rs775804620
NM_005732.4(RAD50):c.81C>T (p.Phe27=) rs868228536
NM_005732.4(RAD50):c.885+10G>C rs1438201235
NM_005732.4(RAD50):c.885+8G>A rs1580991950
NM_005732.4(RAD50):c.933C>T (p.His311=) rs1580992154
NM_005732.4(RAD50):c.964T>C (p.Leu322=) rs1580992200
NM_005732.4(RAD50):c.975T>C (p.Cys325=) rs1296078035
NM_005732.4(RAD50):c.978T>C (p.His326=) rs878854804

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