List of variants in gene RAD51C reported as uncertain significance for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 76

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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.431T>C (p.Ile144Thr)	rs28363307	0.00010
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.428A>G (p.Gln143Arg)	rs587780255	0.00006
NM_058216.3(RAD51C):c.492T>G (p.Phe164Leu)	rs573992101	0.00006
NM_058216.3(RAD51C):c.870T>A (p.Ile290=)	rs376402418	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.1118A>C (p.Glu373Ala)	rs758223998	0.00003
NM_058216.3(RAD51C):c.77A>T (p.Lys26Met)	rs746026526	0.00003
NM_058216.3(RAD51C):c.451G>A (p.Val151Met)	rs753912045	0.00002
NM_058216.3(RAD51C):c.746G>A (p.Arg249His)	rs730881925	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.1097G>A (p.Arg366Gln)	rs577852020	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.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.497T>C (p.Val166Ala)	rs765300465	0.00001
NM_058216.3(RAD51C):c.523G>A (p.Ala175Thr)	rs587780838	0.00001
NM_058216.3(RAD51C):c.563A>T (p.Lys188Met)	rs587781680	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.772C>T (p.Arg258Cys)	rs587782474	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.1016T>A (p.Phe339Tyr)
NM_058216.3(RAD51C):c.1026+6T>A	rs2144046795
NM_058216.3(RAD51C):c.1027-2A>G	rs587780835
NM_058216.3(RAD51C):c.1042G>A (p.Asp348Asn)	rs1555605533
NM_058216.3(RAD51C):c.1103G>A (p.Arg368Gln)	rs1378390389
NM_058216.3(RAD51C):c.1128A>G (p.Leu376=)	rs545024029
NM_058216.3(RAD51C):c.127C>T (p.Pro43Ser)	rs1442559963
NM_058216.3(RAD51C):c.141C>G (p.Ser47Arg)	rs568912602
NM_058216.3(RAD51C):c.186A>C (p.Gln62His)	rs28363303
NM_058216.3(RAD51C):c.249G>C (p.Lys83Asn)	rs145387081
NM_058216.3(RAD51C):c.265G>A (p.Glu89Lys)	rs876658197
NM_058216.3(RAD51C):c.276G>C (p.Glu92Asp)
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.337G>C (p.Gly113Arg)	rs2047954842
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.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.433C>T (p.Pro145Ser)	rs1555594594
NM_058216.3(RAD51C):c.463G>A (p.Ala155Thr)	rs755879664
NM_058216.3(RAD51C):c.477T>G (p.Asp159Glu)	rs760436864
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.718A>T (p.Ile240Leu)	rs863224806
NM_058216.3(RAD51C):c.745C>T (p.Arg249Cys)	rs28363311
NM_058216.3(RAD51C):c.757G>A (p.Asp253Asn)
NM_058216.3(RAD51C):c.797C>T (p.Ala266Val)	rs1555599239
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.919C>T (p.His307Tyr)	rs2049021432
NM_058216.3(RAD51C):c.952G>A (p.Asp318Asn)	rs876659875
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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