ClinVar Miner

List of variants in gene RAD51C reported by Hereditary Cancer Group, L’Institut d'Investigació Biomèdica de Bellvitge

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Total variants: 40
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HGVS dbSNP gnomAD frequency
GRCh37/hg19 17q22(chr17:56809845-56811583)
NM_058216.3(RAD51C):c.-13_14del (p.Met1_Thr5del) rs2143670048
NM_058216.3(RAD51C):c.1009G>T (p.Val337Leu) rs2049473367
NM_058216.3(RAD51C):c.13A>T (p.Thr5Ser) rs1314517659
NM_058216.3(RAD51C):c.308T>A (p.Phe103Tyr) rs2143723981
NM_058216.3(RAD51C):c.310T>C (p.Cys104Arg) rs2047952776
NM_058216.3(RAD51C):c.348C>G (p.Pro116=) rs2047955792
NM_058216.3(RAD51C):c.388G>A (p.Gly130Arg) rs773293999
NM_058216.3(RAD51C):c.398A>G (p.Gln133Arg) rs2143727988
NM_058216.3(RAD51C):c.404+1G>C rs1555593939
NM_058216.3(RAD51C):c.405_571del rs2143742992
NM_058216.3(RAD51C):c.425T>C (p.Val142Ala) rs2143744027
NM_058216.3(RAD51C):c.467T>G (p.Val156Gly) rs1435180142
NM_058216.3(RAD51C):c.472A>T (p.Ile158Phe) rs771888635
NM_058216.3(RAD51C):c.472dup (p.Ile158fs) rs2143746162
NM_058216.3(RAD51C):c.489T>G (p.Ser163Arg) rs876659719
NM_058216.3(RAD51C):c.522_523insC (p.Ala175fs) rs2143748292
NM_058216.3(RAD51C):c.572-1G>T rs1413872299
NM_058216.3(RAD51C):c.586T>C (p.Leu196=) rs2143796827
NM_058216.3(RAD51C):c.65C>T (p.Ala22Val) rs2143676047
NM_058216.3(RAD51C):c.706-1G>A rs1555599090
NM_058216.3(RAD51C):c.706_837+2del rs2143849978
NM_058216.3(RAD51C):c.708_837+2del
NM_058216.3(RAD51C):c.752A>G (p.Asp251Gly) rs2048496443
NM_058216.3(RAD51C):c.801G>A (p.Gln267=) rs2048499866
NM_058216.3(RAD51C):c.801del (p.Gln267fs) rs2143853790
NM_058216.3(RAD51C):c.837+5G>T rs1567799952
NM_058216.3(RAD51C):c.862del (p.Thr288fs) rs2143930413
NM_058216.3(RAD51C):c.871G>A (p.Asp291Asn) rs2143930779
NM_058216.3(RAD51C):c.882G>C (p.Gln294His) rs2143931255
NM_058216.3(RAD51C):c.89C>A (p.Ala30Glu) rs1000113630
NM_058216.3(RAD51C):c.945dup (p.His316fs) rs2143962519
NM_058216.3(RAD51C):c.947A>G (p.His316Arg) rs2143962686
NM_058216.3(RAD51C):c.966delG rs2144044105
NM_058216.3:c.1_571del
NM_058216.3:c.1_705del
NM_058216.3:c.838_965dup
NM_058216.3:c.905_966del
NM_058216.3:c.966_1027del
c.706-4423_1131+7851del;p.(Val236_Leu376delins11)

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