ClinVar Miner

List of variants in gene RAD51C reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (891):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 78
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HGVS dbSNP
NM_058216.2(RAD51C):c.*25C>G rs28363336
NM_058216.2(RAD51C):c.-26C>T rs12946397
NM_058216.2(RAD51C):c.1008A>G (p.Thr336=) rs1057521598
NM_058216.2(RAD51C):c.1059T>C (p.Ser353=) rs1399862812
NM_058216.2(RAD51C):c.1062A>G (p.Ala354=) rs201000407
NM_058216.2(RAD51C):c.1089G>A (p.Leu363=) rs559647198
NM_058216.2(RAD51C):c.114C>T (p.Leu38=) rs786202265
NM_058216.2(RAD51C):c.129C>G (p.Pro43=) rs1555592066
NM_058216.2(RAD51C):c.141C>T (p.Ser47=) rs568912602
NM_058216.2(RAD51C):c.145+12T>G rs377297129
NM_058216.2(RAD51C):c.146-15T>C rs1036386535
NM_058216.2(RAD51C):c.186A>G (p.Gln62=) rs28363303
NM_058216.2(RAD51C):c.189T>C (p.Ile63=) rs730881923
NM_058216.2(RAD51C):c.195A>G (p.Arg65=) rs45511291
NM_058216.2(RAD51C):c.207C>T (p.Leu69=) rs1057523582
NM_058216.2(RAD51C):c.225T>C (p.Tyr75=) rs1555593553
NM_058216.2(RAD51C):c.234A>G (p.Thr78=) rs730881929
NM_058216.2(RAD51C):c.240G>A (p.Glu80=) rs779053608
NM_058216.2(RAD51C):c.252G>A (p.Lys84=) rs786202890
NM_058216.2(RAD51C):c.258A>T (p.Thr86=) rs149228565
NM_058216.2(RAD51C):c.262C>T (p.Leu88=) rs786201383
NM_058216.2(RAD51C):c.270T>C (p.Leu90=) rs1555593651
NM_058216.2(RAD51C):c.315A>G (p.Ser105=) rs876660032
NM_058216.2(RAD51C):c.318A>C (p.Ala106=) rs781371468
NM_058216.2(RAD51C):c.319C>T (p.Leu107=) rs752817595
NM_058216.2(RAD51C):c.336G>A (p.Gly112=) rs746122031
NM_058216.2(RAD51C):c.336G>C (p.Gly112=) rs746122031
NM_058216.2(RAD51C):c.342A>G (p.Gly114=) rs1555593777
NM_058216.2(RAD51C):c.351A>G (p.Leu117=) rs370986989
NM_058216.2(RAD51C):c.357A>G (p.Lys119=) rs863224434
NM_058216.2(RAD51C):c.363A>G (p.Thr121=) rs876659626
NM_058216.2(RAD51C):c.376G>A (p.Ala126Thr) rs61758784
NM_058216.2(RAD51C):c.396A>C (p.Thr132=) rs766221834
NM_058216.2(RAD51C):c.400T>C (p.Leu134=) rs863224435
NM_058216.2(RAD51C):c.405-8G>A rs1431351072
NM_058216.2(RAD51C):c.405T>C (p.Cys135=) rs537272666
NM_058216.2(RAD51C):c.417A>G (p.Ala139=) rs863224436
NM_058216.2(RAD51C):c.420A>G (p.Val140=) rs1060504672
NM_058216.2(RAD51C):c.435A>G (p.Pro145=) rs555235745
NM_058216.2(RAD51C):c.453G>A (p.Val151=) rs45553636
NM_058216.2(RAD51C):c.477T>C (p.Asp159=) rs760436864
NM_058216.2(RAD51C):c.480A>G (p.Thr160=) rs1060504670
NM_058216.2(RAD51C):c.513C>T (p.Asp171=) rs140279158
NM_058216.2(RAD51C):c.546T>G (p.Leu182=) rs1476282276
NM_058216.2(RAD51C):c.54G>T (p.Pro18=) rs1555591865
NM_058216.2(RAD51C):c.564G>A (p.Lys188=) rs876658264
NM_058216.2(RAD51C):c.570G>A (p.Glu190=) rs1555594937
NM_058216.2(RAD51C):c.571+16A>G rs141621051
NM_058216.2(RAD51C):c.651A>T (p.Thr217=) rs757915374
NM_058216.2(RAD51C):c.654G>A (p.Glu218=) rs1388636466
NM_058216.2(RAD51C):c.658C>T (p.Leu220=) rs1555597205
NM_058216.2(RAD51C):c.705+10A>G rs377586976
NM_058216.2(RAD51C):c.706-13C>G rs747406535
NM_058216.2(RAD51C):c.706-18T>C rs56401264
NM_058216.2(RAD51C):c.706-6A>G rs776931174
NM_058216.2(RAD51C):c.706-7T>C rs1555599087
NM_058216.2(RAD51C):c.706-9T>C rs1060504671
NM_058216.2(RAD51C):c.717G>C (p.Val239=) rs1555599108
NM_058216.2(RAD51C):c.744T>C (p.Phe248=) rs150142859
NM_058216.2(RAD51C):c.756A>G (p.Leu252=) rs863224437
NM_058216.2(RAD51C):c.783A>G (p.Leu261=) rs138643096
NM_058216.2(RAD51C):c.78G>A (p.Lys26=) rs864622460
NM_058216.2(RAD51C):c.790G>A (p.Gly264Ser) rs147241704
NM_058216.2(RAD51C):c.837+14A>G rs1057517644
NM_058216.2(RAD51C):c.837+7A>G rs1555599293
NM_058216.2(RAD51C):c.840A>G (p.Val280=) rs756503509
NM_058216.2(RAD51C):c.859A>G (p.Thr287Ala) rs28363317
NM_058216.2(RAD51C):c.870T>A (p.Ile290=) rs376402418
NM_058216.2(RAD51C):c.879T>C (p.Asn293=) rs1555602132
NM_058216.2(RAD51C):c.87T>C (p.Ser29=) rs786203249
NM_058216.2(RAD51C):c.904+7A>C rs1555602171
NM_058216.2(RAD51C):c.905-7C>T rs757624360
NM_058216.2(RAD51C):c.90G>A (p.Ala30=) rs115414895
NM_058216.2(RAD51C):c.945T>C (p.Phe315=) rs201235884
NM_058216.2(RAD51C):c.966-4G>C rs878855183
NM_058216.2(RAD51C):c.967T>C (p.Leu323=) rs747727600
NM_058216.2(RAD51C):c.9G>C (p.Gly3=) rs751117852
NM_058216.3(RAD51C):c.537C>T (p.His179=) rs372385738

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