ClinVar Miner

List of variants in gene RAD51C reported as uncertain significance by Baylor Genetics

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Gene type:
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Total variants: 94
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HGVS dbSNP gnomAD frequency
NM_058216.3(RAD51C):c.922G>T (p.Ala308Ser) rs185057307 0.00025
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.431T>C (p.Ile144Thr) rs28363307 0.00010
NM_058216.3(RAD51C):c.1108C>T (p.Arg370Ter) rs756744016 0.00006
NM_058216.3(RAD51C):c.14C>T (p.Thr5Met) rs201523760 0.00006
NM_058216.3(RAD51C):c.428A>G (p.Gln143Arg) rs587780255 0.00006
NM_058216.3(RAD51C):c.492T>G (p.Phe164Leu) rs573992101 0.00006
NM_058216.3(RAD51C):c.34C>T (p.Arg12Trp) rs28910276 0.00004
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.1090A>G (p.Ser364Gly) rs587782565 0.00003
NM_058216.3(RAD51C):c.451G>C (p.Val151Leu) rs753912045 0.00003
NM_058216.3(RAD51C):c.106G>A (p.Glu36Lys) rs773998134 0.00002
NM_058216.3(RAD51C):c.1117G>A (p.Glu373Lys) rs1433497291 0.00002
NM_058216.3(RAD51C):c.451G>A (p.Val151Met) rs753912045 0.00002
NM_058216.3(RAD51C):c.537C>A (p.His179Gln) rs372385738 0.00002
NM_058216.3(RAD51C):c.571+5G>A rs145779113 0.00002
NM_058216.3(RAD51C):c.719T>C (p.Ile240Thr) rs539341386 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.923C>G (p.Ala308Gly) rs786203498 0.00002
NM_058216.3(RAD51C):c.1097G>A (p.Arg366Gln) rs577852020 0.00001
NM_058216.3(RAD51C):c.1109G>A (p.Arg370Gln) rs373170458 0.00001
NM_058216.3(RAD51C):c.154A>C (p.Ile52Leu) rs730881927 0.00001
NM_058216.3(RAD51C):c.233C>T (p.Thr78Ile) rs112832782 0.00001
NM_058216.3(RAD51C):c.28A>T (p.Met10Leu) rs1452865935 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.487A>G (p.Ser163Gly) rs776904180 0.00001
NM_058216.3(RAD51C):c.523G>A (p.Ala175Thr) rs587780838 0.00001
NM_058216.3(RAD51C):c.548T>C (p.Ile183Thr) rs756727559 0.00001
NM_058216.3(RAD51C):c.563A>T (p.Lys188Met) rs587781680 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.748C>T (p.His250Tyr) rs531540031 0.00001
NM_058216.3(RAD51C):c.758A>G (p.Asp253Gly) rs1060502592 0.00001
NM_058216.3(RAD51C):c.772C>T (p.Arg258Cys) rs587782474 0.00001
NM_058216.3(RAD51C):c.779G>A (p.Arg260Gln) rs730881926 0.00001
NM_058216.3(RAD51C):c.935G>A (p.Arg312Gln) rs779834376 0.00001
NM_058216.3(RAD51C):c.1006A>G (p.Thr336Ala) rs772344354
NM_058216.3(RAD51C):c.101C>T (p.Thr34Ile) rs762230288
NM_058216.3(RAD51C):c.1026+6T>A rs2144046795
NM_058216.3(RAD51C):c.1027-3C>G rs587782459
NM_058216.3(RAD51C):c.1074_1110del (p.Glu360fs) rs1343626760
NM_058216.3(RAD51C):c.1103G>A (p.Arg368Gln) rs1378390389
NM_058216.3(RAD51C):c.118G>A (p.Glu40Lys) rs786204086
NM_058216.3(RAD51C):c.133G>A (p.Glu45Lys)
NM_058216.3(RAD51C):c.146-4_146-2del rs1555593450
NM_058216.3(RAD51C):c.14C>G (p.Thr5Arg) rs201523760
NM_058216.3(RAD51C):c.158C>G (p.Ser53Cys) rs876659265
NM_058216.3(RAD51C):c.199G>C (p.Glu67Gln) rs1567785872
NM_058216.3(RAD51C):c.212A>C (p.Asn71Thr) rs1598455555
NM_058216.3(RAD51C):c.212A>G (p.Asn71Ser) rs1598455555
NM_058216.3(RAD51C):c.217C>T (p.Pro73Ser) rs1555593541
NM_058216.3(RAD51C):c.245A>G (p.His82Arg) rs1555593600
NM_058216.3(RAD51C):c.254G>A (p.Cys85Tyr) rs1555593627
NM_058216.3(RAD51C):c.274G>A (p.Glu92Lys) rs765304898
NM_058216.3(RAD51C):c.283C>T (p.His95Tyr) rs1317173760
NM_058216.3(RAD51C):c.293G>C (p.Gly98Ala) rs1060502586
NM_058216.3(RAD51C):c.293G>T (p.Gly98Val) rs1060502586
NM_058216.3(RAD51C):c.29T>C (p.Met10Thr) rs730881936
NM_058216.3(RAD51C):c.335G>A (p.Gly112Glu) rs370212314
NM_058216.3(RAD51C):c.335G>C (p.Gly112Ala) rs370212314
NM_058216.3(RAD51C):c.344T>C (p.Val115Ala) rs779104845
NM_058216.3(RAD51C):c.373G>A (p.Gly125Ser) rs142058115
NM_058216.3(RAD51C):c.395C>G (p.Thr132Arg) rs730881930
NM_058216.3(RAD51C):c.397C>A (p.Gln133Lys) rs387907159
NM_058216.3(RAD51C):c.407T>G (p.Met136Arg) rs2048021034
NM_058216.3(RAD51C):c.416C>T (p.Ala139Val) rs1567788274
NM_058216.3(RAD51C):c.422A>T (p.Asp141Val)
NM_058216.3(RAD51C):c.475G>C (p.Asp159His)
NM_058216.3(RAD51C):c.535C>A (p.His179Asn)
NM_058216.3(RAD51C):c.571+3_571+6del
NM_058216.3(RAD51C):c.598A>G (p.Thr200Ala) rs1369125082
NM_058216.3(RAD51C):c.718A>T (p.Ile240Leu) rs863224806
NM_058216.3(RAD51C):c.71G>A (p.Arg24Gln) rs777554369
NM_058216.3(RAD51C):c.724G>A (p.Asp242Asn) rs876659188
NM_058216.3(RAD51C):c.742T>C (p.Phe248Leu) rs876659496
NM_058216.3(RAD51C):c.779G>C (p.Arg260Pro) rs730881926
NM_058216.3(RAD51C):c.826C>A (p.His276Asn) rs1567799906
NM_058216.3(RAD51C):c.835G>C (p.Ala279Pro) rs587782507
NM_058216.3(RAD51C):c.86C>T (p.Ser29Phe) rs876659683
NM_058216.3(RAD51C):c.875G>A (p.Arg292Lys)
NM_058216.3(RAD51C):c.884C>G (p.Ala295Gly) rs1555602136
NM_058216.3(RAD51C):c.89C>T (p.Ala30Val) rs1000113630
NM_058216.3(RAD51C):c.905-7C>G
NM_058216.3(RAD51C):c.920A>G (p.His307Arg) rs2049021589
NM_058216.3(RAD51C):c.960G>C (p.Lys320Asn) rs864622395
NM_058216.3(RAD51C):c.965G>C (p.Arg322Thr) rs1555603059
NM_058216.3(RAD51C):c.973A>G (p.Thr325Ala) rs1555605054
NM_058216.3(RAD51C):c.978G>C (p.Leu326Phe) rs770652503
NM_058216.3(RAD51C):c.980A>G (p.Tyr327Cys) rs1598534951
NM_058216.3(RAD51C):c.989C>G (p.Pro330Arg) rs1567817392

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