ClinVar Miner

List of variants in gene RAD51C reported as likely pathogenic for breast-ovarian cancer, familial, susceptibility to, 3

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 120
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_058216.3(RAD51C):c.774del (p.Thr259fs) rs754367349 0.00004
NM_058216.3(RAD51C):c.571+5G>A rs145779113 0.00003
NM_058216.3(RAD51C):c.706-2A>G rs587780259 0.00002
NM_058216.3(RAD51C):c.773G>A (p.Arg258His) rs267606997 0.00002
NM_058216.3(RAD51C):c.837+1G>A rs760235677 0.00002
NM_058216.3(RAD51C):c.340G>A (p.Gly114Arg) rs786203690 0.00001
NM_058216.3(RAD51C):c.403T>C (p.Cys135Arg) rs878855178 0.00001
NM_058216.3(RAD51C):c.404+2T>C rs730881931 0.00001
NM_058216.3(RAD51C):c.414G>C (p.Leu138Phe) rs267606999 0.00001
NM_058216.3(RAD51C):c.458G>A (p.Gly153Asp) rs765730332 0.00001
NM_058216.3(RAD51C):c.572-2A>G rs145310733 0.00001
NM_058216.3(RAD51C):c.835G>C (p.Ala279Pro) rs587782507 0.00001
NM_058216.3(RAD51C):c.904+5G>T rs587782702 0.00001
NM_058216.3(RAD51C):c.905-2A>C rs779582317 0.00001
NM_058216.3(RAD51C):c.905-2_905-1del rs587781995 0.00001
NM_058216.3(RAD51C):c.905-2del rs876658652 0.00001
NM_058216.3(RAD51C):c.914G>A (p.Trp305Ter) rs876659874 0.00001
NM_058216.3(RAD51C):c.934C>T (p.Arg312Trp) rs730881932 0.00001
NM_058216.3(RAD51C):c.1018C>T (p.Gln340Ter) rs1555605103
NM_058216.3(RAD51C):c.1026+1G>C rs1567817516
NM_058216.3(RAD51C):c.1026+5_1026+7del rs587781410
NM_058216.3(RAD51C):c.145+1G>A rs757128712
NM_058216.3(RAD51C):c.145+1G>C rs757128712
NM_058216.3(RAD51C):c.145+1G>T rs757128712
NM_058216.3(RAD51C):c.146-2A>G rs1555593457
NM_058216.3(RAD51C):c.146-4_146-2del rs1555593450
NM_058216.3(RAD51C):c.168del (p.Ala57fs) rs2143717943
NM_058216.3(RAD51C):c.222A>G (p.Arg74=) rs2047945471
NM_058216.3(RAD51C):c.224_225dup (p.Ala76fs) rs1598455598
NM_058216.3(RAD51C):c.250A>T (p.Lys84Ter) rs1555593616
NM_058216.3(RAD51C):c.305C>T (p.Thr102Ile) rs755106004
NM_058216.3(RAD51C):c.323A>G (p.Asp108Gly) rs1555593745
NM_058216.3(RAD51C):c.341G>T (p.Gly114Val) rs1555593767
NM_058216.3(RAD51C):c.379_380insG (p.Pro127fs) rs2047958236
NM_058216.3(RAD51C):c.388G>A (p.Gly130Arg) rs773293999
NM_058216.3(RAD51C):c.388G>C (p.Gly130Arg) rs773293999
NM_058216.3(RAD51C):c.389G>A (p.Gly130Glu)
NM_058216.3(RAD51C):c.389G>C (p.Gly130Ala) rs2047958982
NM_058216.3(RAD51C):c.392A>T (p.Lys131Ile) rs762761380
NM_058216.3(RAD51C):c.394A>C (p.Thr132Pro) rs2047959481
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.399dup (p.Leu134fs) rs2509276440
NM_058216.3(RAD51C):c.404+1G>A rs1555593939
NM_058216.3(RAD51C):c.404+1G>C rs1555593939
NM_058216.3(RAD51C):c.404G>A (p.Cys135Tyr) rs767796996
NM_058216.3(RAD51C):c.404G>C (p.Cys135Ser) rs767796996
NM_058216.3(RAD51C):c.404G>T (p.Cys135Phe) rs767796996
NM_058216.3(RAD51C):c.405-1G>A rs587782036
NM_058216.3(RAD51C):c.405-1G>C rs587782036
NM_058216.3(RAD51C):c.405-1G>T rs587782036
NM_058216.3(RAD51C):c.405-6T>A rs1064793245
NM_058216.3(RAD51C):c.405T>G (p.Cys135Trp) rs537272666
NM_058216.3(RAD51C):c.409C>T (p.Gln137Ter) rs2048021234
NM_058216.3(RAD51C):c.446GAG[1] (p.Gly150del) rs2048024043
NM_058216.3(RAD51C):c.447_448delinsT (p.Gly150fs) rs1598460178
NM_058216.3(RAD51C):c.448G>A (p.Gly150Arg) rs553112850
NM_058216.3(RAD51C):c.449G>A (p.Gly150Glu) rs730881934
NM_058216.3(RAD51C):c.449G>T (p.Gly150Val)
NM_058216.3(RAD51C):c.467T>A (p.Val156Asp) rs1435180142
NM_058216.3(RAD51C):c.472dup (p.Ile158fs) rs2143746162
NM_058216.3(RAD51C):c.485G>A (p.Gly162Glu) rs35151472
NM_058216.3(RAD51C):c.491T>C (p.Phe164Ser) rs1060502589
NM_058216.3(RAD51C):c.502A>G (p.Arg168Gly) rs587781490
NM_058216.3(RAD51C):c.504A>C (p.Arg168Ser)
NM_058216.3(RAD51C):c.519dup (p.Thr174fs) rs1598460710
NM_058216.3(RAD51C):c.532C>T (p.Gln178Ter) rs1555594861
NM_058216.3(RAD51C):c.535del (p.His179fs) rs1555594864
NM_058216.3(RAD51C):c.561dup (p.Lys188fs) rs2509283581
NM_058216.3(RAD51C):c.570_571+16del rs2509283705
NM_058216.3(RAD51C):c.571+1G>T rs746870368
NM_058216.3(RAD51C):c.571+1del rs1327086366
NM_058216.3(RAD51C):c.571G>T (p.Glu191Ter) rs1598460983
NM_058216.3(RAD51C):c.572-1G>C rs1413872299
NM_058216.3(RAD51C):c.572-1G>T rs1413872299
NM_058216.3(RAD51C):c.589G>T (p.Glu197Ter) rs1555597094
NM_058216.3(RAD51C):c.706-1G>A rs1555599090
NM_058216.3(RAD51C):c.706-1G>C rs1555599090
NM_058216.3(RAD51C):c.706-1G>T rs1555599090
NM_058216.3(RAD51C):c.706-2A>C rs587780259
NM_058216.3(RAD51C):c.708_837+2del rs2509312694
NM_058216.3(RAD51C):c.710G>C (p.Arg237Pro) rs370393672
NM_058216.3(RAD51C):c.724G>A (p.Asp242Asn) rs876659188
NM_058216.3(RAD51C):c.801del (p.Gln267fs) rs2143853790
NM_058216.3(RAD51C):c.80T>C (p.Leu27Pro) rs587781309
NM_058216.3(RAD51C):c.829A>T (p.Arg277Ter) rs2143854758
NM_058216.3(RAD51C):c.82dup (p.Val28fs) rs2143677258
NM_058216.3(RAD51C):c.837+1G>C rs760235677
NM_058216.3(RAD51C):c.837+1G>T rs760235677
NM_058216.3(RAD51C):c.837+1_837+13del rs2048502560
NM_058216.3(RAD51C):c.837+1del rs1555599288
NM_058216.3(RAD51C):c.837+4_837+7del rs727503760
NM_058216.3(RAD51C):c.837+5G>T rs1567799952
NM_058216.3(RAD51C):c.838-1G>C rs2143929613
NM_058216.3(RAD51C):c.838-2A>G rs748589398
NM_058216.3(RAD51C):c.838-2A>T rs748589398
NM_058216.3(RAD51C):c.851_854dup (p.Met286fs) rs1060502605
NM_058216.3(RAD51C):c.860del (p.Thr287fs) rs2143930383
NM_058216.3(RAD51C):c.904+1G>A rs1555602159
NM_058216.3(RAD51C):c.904+1G>T rs1555602159
NM_058216.3(RAD51C):c.904G>A (p.Gly302Arg) rs1555602158
NM_058216.3(RAD51C):c.905-2A>G rs779582317
NM_058216.3(RAD51C):c.905-3_906del rs730881941
NM_058216.3(RAD51C):c.905_908dup (p.Ser304fs) rs2509343956
NM_058216.3(RAD51C):c.929_939del (p.Thr310fs) rs2509344172
NM_058216.3(RAD51C):c.934C>G (p.Arg312Gly) rs730881932
NM_058216.3(RAD51C):c.942_948del (p.Phe315fs) rs1479360028
NM_058216.3(RAD51C):c.952del (p.Asp318fs) rs2509344483
NM_058216.3(RAD51C):c.959del (p.Lys320fs) rs2509344581
NM_058216.3(RAD51C):c.964del (p.Arg322fs) rs1555603056
NM_058216.3(RAD51C):c.965+1G>A rs730881933
NM_058216.3(RAD51C):c.965+1del rs2509344663
NM_058216.3(RAD51C):c.965+5G>A rs774586107
NM_058216.3(RAD51C):c.965+5G>C
NM_058216.3(RAD51C):c.966delG rs2144044105
NM_058216.3(RAD51C):c.974delinsAA (p.Thr325fs) rs2509363942
NM_058216.3:c.(705+1_706-1)_(1131+1_?)del
NM_058216.3:c.-20_705+5del
NM_058216.3:c.1_571del
NM_058216.3:c.905_966del

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.