ClinVar Miner

List of variants in gene RAD51C studied for Hereditary breast ovarian cancer syndrome

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Total variants: 73
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HGVS dbSNP gnomAD frequency
NM_058216.3(RAD51C):c.404+63_404+71dup rs142735413 0.00694
NM_058216.3(RAD51C):c.859A>G (p.Thr287Ala) rs28363317 0.00653
NM_058216.3(RAD51C):c.790G>A (p.Gly264Ser) rs147241704 0.00207
NM_058216.3(RAD51C):c.146-8A>G rs201079501 0.00074
NM_058216.3(RAD51C):c.258A>T (p.Thr86=) rs149228565 0.00017
NM_058216.3(RAD51C):c.404+71G>A rs376780225 0.00009
NM_058216.3(RAD51C):c.506T>C (p.Val169Ala) rs587780256 0.00009
NM_058216.3(RAD51C):c.134A>G (p.Glu45Gly) rs587781383 0.00006
NM_058216.3(RAD51C):c.428A>G (p.Gln143Arg) rs587780255 0.00006
NM_058216.3(RAD51C):c.870T>A (p.Ile290=) rs376402418 0.00006
NM_058216.3(RAD51C):c.577C>T (p.Arg193Ter) rs200293302 0.00004
NM_058216.3(RAD51C):c.1102C>T (p.Arg368Trp) rs587780253 0.00003
NM_058216.3(RAD51C):c.783A>G (p.Leu261=) rs138643096 0.00003
NM_058216.3(RAD51C):c.7G>A (p.Gly3Arg) rs376403182 0.00003
NM_058216.3(RAD51C):c.224dup (p.Tyr75Ter) rs730881939 0.00002
NM_058216.3(RAD51C):c.706-2A>G rs587780259 0.00002
NM_058216.3(RAD51C):c.719T>C (p.Ile240Thr) rs539341386 0.00002
NM_058216.3(RAD51C):c.773G>A (p.Arg258His) rs267606997 0.00002
NM_058216.3(RAD51C):c.1051G>A (p.Val351Ile) rs1160208500 0.00001
NM_058216.3(RAD51C):c.141C>T (p.Ser47=) rs568912602 0.00001
NM_058216.3(RAD51C):c.404+2T>C rs730881931 0.00001
NM_058216.3(RAD51C):c.406A>T (p.Met136Leu) rs587780254 0.00001
NM_058216.3(RAD51C):c.523G>A (p.Ala175Thr) rs587780838 0.00001
NM_058216.3(RAD51C):c.547A>G (p.Ile183Val) rs753475114 0.00001
NM_058216.3(RAD51C):c.571+4A>G rs587780257 0.00001
NM_058216.3(RAD51C):c.709C>T (p.Arg237Ter) rs770637624 0.00001
NM_058216.3(RAD51C):c.730A>G (p.Ile244Val) rs199886026 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.934C>T (p.Arg312Trp) rs730881932 0.00001
NM_058216.3(RAD51C):c.935G>A (p.Arg312Gln) rs779834376 0.00001
NM_058216.3(RAD51C):c.97C>T (p.Gln33Ter) rs587782528 0.00001
NM_058216.3(RAD51C):c.9G>C (p.Gly3=) rs751117852 0.00001
NC_000017.10:g.(56774221_56780556)_(56811704_?)del
NC_000017.10:g.(56780691_56787219)_(56801462_56809844)dup
NC_000017.10:g.(56780691_56787219)_(56812973_?)del
NC_000017.10:g.(56787352_56798106)_(56812973_?)del
NC_000017.10:g.(56801462_56809844)_(56809906_56811478)del
NC_000017.10:g.(?_56780557)_(56780690_?)del
NM_058216.3(RAD51C):c.1026+5_1026+7del rs587781410
NM_058216.3(RAD51C):c.1033G>C (p.Gly345Arg)
NM_058216.3(RAD51C):c.1034G>T (p.Gly345Val)
NM_058216.3(RAD51C):c.104C>G (p.Ala35Gly) rs1555592011
NM_058216.3(RAD51C):c.133G>T (p.Glu45Ter) rs1598449660
NM_058216.3(RAD51C):c.186_187del (p.Gln62fs) rs587782170
NM_058216.3(RAD51C):c.20G>C (p.Arg7Pro) rs892567748
NM_058216.3(RAD51C):c.224_225dup (p.Ala76fs) rs1598455598
NM_058216.3(RAD51C):c.307T>G (p.Phe103Val) rs1114167446
NM_058216.3(RAD51C):c.32A>G (p.Gln11Arg) rs730881937
NM_058216.3(RAD51C):c.374G>T (p.Gly125Val) rs267606998
NM_058216.3(RAD51C):c.386T>C (p.Val129Ala) rs876660641
NM_058216.3(RAD51C):c.394A>C (p.Thr132Pro) rs2047959481
NM_058216.3(RAD51C):c.397C>T (p.Gln133Ter) rs387907159
NM_058216.3(RAD51C):c.3G>C (p.Met1Ile) rs769053886
NM_058216.3(RAD51C):c.404+44A>G
NM_058216.3(RAD51C):c.404+44_404+45del rs746082340
NM_058216.3(RAD51C):c.404+91A>G
NM_058216.3(RAD51C):c.404+92T>C
NM_058216.3(RAD51C):c.404G>A (p.Cys135Tyr) rs767796996
NM_058216.3(RAD51C):c.493A>G (p.Met165Val) rs1555594766
NM_058216.3(RAD51C):c.532C>T (p.Gln178Ter) rs1555594861
NM_058216.3(RAD51C):c.571+1del rs1327086366
NM_058216.3(RAD51C):c.572-11del rs587780258
NM_058216.3(RAD51C):c.68T>G (p.Val23Gly) rs2047807604
NM_058216.3(RAD51C):c.706-1G>A rs1555599090
NM_058216.3(RAD51C):c.724G>A (p.Asp242Asn) rs876659188
NM_058216.3(RAD51C):c.732del (p.Ile244fs) rs1060502601
NM_058216.3(RAD51C):c.760G>T (p.Asp254Tyr) rs1567799662
NM_058216.3(RAD51C):c.837+1G>C rs760235677
NM_058216.3(RAD51C):c.837+1G>T rs760235677
NM_058216.3(RAD51C):c.890_899del (p.Leu297fs) rs1555602141
NM_058216.3(RAD51C):c.904G>A (p.Gly302Arg) rs1555602158
NM_058216.3(RAD51C):c.93del (p.Phe32fs) rs730881942

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