ClinVar Miner

List of variants in gene RAD51C reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Gene type:
ClinVar version:
Total variants: 62
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HGVS dbSNP gnomAD frequency
NM_058216.3(RAD51C):c.890T>C (p.Leu297Pro) rs143026267 0.00017
NM_058216.3(RAD51C):c.784T>G (p.Leu262Val) rs149331537 0.00014
NM_058216.3(RAD51C):c.200A>G (p.Glu67Gly) rs375451955 0.00012
NM_058216.3(RAD51C):c.134A>G (p.Glu45Gly) rs587781383 0.00006
NM_058216.3(RAD51C):c.14C>T (p.Thr5Met) rs201523760 0.00006
NM_058216.3(RAD51C):c.492T>G (p.Phe164Leu) rs573992101 0.00006
NM_058216.3(RAD51C):c.721G>A (p.Val241Met) rs184033132 0.00004
NM_058216.3(RAD51C):c.956G>A (p.Arg319Gln) rs367846829 0.00004
NM_058216.3(RAD51C):c.1102C>T (p.Arg368Trp) rs587780253 0.00003
NM_058216.3(RAD51C):c.77A>T (p.Lys26Met) rs746026526 0.00003
NM_058216.3(RAD51C):c.397C>G (p.Gln133Glu) rs387907159 0.00002
NM_058216.3(RAD51C):c.746G>A (p.Arg249His) rs730881925 0.00002
NM_058216.3(RAD51C):c.778C>T (p.Arg260Trp) rs374196453 0.00002
NM_058216.3(RAD51C):c.1027-3C>T rs587782459 0.00001
NM_058216.3(RAD51C):c.1096C>T (p.Arg366Trp) rs587782449 0.00001
NM_058216.3(RAD51C):c.1109G>A (p.Arg370Gln) rs373170458 0.00001
NM_058216.3(RAD51C):c.121G>A (p.Val41Met) rs879254131 0.00001
NM_058216.3(RAD51C):c.128C>T (p.Pro43Leu) rs766958594 0.00001
NM_058216.3(RAD51C):c.252G>T (p.Lys84Asn) rs786202890 0.00001
NM_058216.3(RAD51C):c.28A>T (p.Met10Leu) rs1452865935 0.00001
NM_058216.3(RAD51C):c.340G>A (p.Gly114Arg) rs786203690 0.00001
NM_058216.3(RAD51C):c.370T>A (p.Cys124Ser) rs1273995533 0.00001
NM_058216.3(RAD51C):c.406A>T (p.Met136Leu) rs587780254 0.00001
NM_058216.3(RAD51C):c.458G>A (p.Gly153Asp) rs765730332 0.00001
NM_058216.3(RAD51C):c.523G>A (p.Ala175Thr) rs587780838 0.00001
NM_058216.3(RAD51C):c.571+4A>G rs587780257 0.00001
NM_058216.3(RAD51C):c.710G>A (p.Arg237Gln) rs370393672 0.00001
NM_058216.3(RAD51C):c.730A>G (p.Ile244Val) rs199886026 0.00001
NM_058216.3(RAD51C):c.73G>A (p.Val25Met) rs757116652 0.00001
NM_058216.3(RAD51C):c.779G>A (p.Arg260Gln) rs730881926 0.00001
NM_058216.3(RAD51C):c.892G>C (p.Val298Leu) rs1555602145 0.00001
NM_058216.3(RAD51C):c.-7G>T rs753249247
NM_058216.3(RAD51C):c.1000G>A (p.Glu334Lys) rs1567817431
NM_058216.3(RAD51C):c.1026+6T>A rs2144046795
NM_058216.3(RAD51C):c.1027-2A>G rs587780835
NM_058216.3(RAD51C):c.1103G>A (p.Arg368Gln) rs1378390389
NM_058216.3(RAD51C):c.249G>C (p.Lys83Asn) rs145387081
NM_058216.3(RAD51C):c.24T>A (p.Phe8Leu) rs587782698
NM_058216.3(RAD51C):c.265G>A (p.Glu89Lys) rs876658197
NM_058216.3(RAD51C):c.32A>G (p.Gln11Arg) rs730881937
NM_058216.3(RAD51C):c.335G>C (p.Gly112Ala) rs370212314
NM_058216.3(RAD51C):c.335G>T (p.Gly112Val) rs370212314
NM_058216.3(RAD51C):c.377C>T (p.Ala126Val) rs1555593858
NM_058216.3(RAD51C):c.389G>C (p.Gly130Ala) rs2047958982
NM_058216.3(RAD51C):c.3G>T (p.Met1Ile) rs769053886
NM_058216.3(RAD51C):c.405-5G>A rs1598459949
NM_058216.3(RAD51C):c.411G>T (p.Gln137His) rs1555594552
NM_058216.3(RAD51C):c.418G>A (p.Val140Ile) rs730881938
NM_058216.3(RAD51C):c.477T>G (p.Asp159Glu) rs760436864
NM_058216.3(RAD51C):c.482A>T (p.Glu161Val) rs1555594725
NM_058216.3(RAD51C):c.487A>T (p.Ser163Cys) rs776904180
NM_058216.3(RAD51C):c.489T>A (p.Ser163Arg) rs876659719
NM_058216.3(RAD51C):c.50T>C (p.Phe17Ser) rs1411454855
NM_058216.3(RAD51C):c.572-3C>G rs1567794089
NM_058216.3(RAD51C):c.71G>A (p.Arg24Gln) rs777554369
NM_058216.3(RAD51C):c.745C>T (p.Arg249Cys) rs28363311
NM_058216.3(RAD51C):c.86C>T (p.Ser29Phe) rs876659683
NM_058216.3(RAD51C):c.901T>G (p.Leu301Val) rs2143932190
NM_058216.3(RAD51C):c.959A>G (p.Lys320Arg) rs587780260
NM_058216.3(RAD51C):c.960G>C (p.Lys320Asn) rs864622395
NM_058216.3(RAD51C):c.966-1G>A rs876658272
NM_058216.3(RAD51C):c.989C>T (p.Pro330Leu) rs1567817392

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