List of variants in gene RAD51C reported as pathogenic for cancer

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.577C>T (p.Arg193Ter)	rs200293302	0.00004
NM_058216.3(RAD51C):c.224dup (p.Tyr75Ter)	rs730881939	0.00002
NM_058216.3(RAD51C):c.837+1G>A	rs760235677	0.00002
NM_058216.3(RAD51C):c.1A>G (p.Met1Val)	rs921435798	0.00001
NM_058216.3(RAD51C):c.709C>T (p.Arg237Ter)	rs770637624	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_058216.2(RAD51C):c.(705+1_706-1)_(837+1_838-1)del
NM_058216.3(RAD51C):c.1026+5_1026+7del	rs587781410
NM_058216.3(RAD51C):c.1027-2A>G	rs587780835
NM_058216.3(RAD51C):c.1129T>C (p.Ter377Gln)
NM_058216.3(RAD51C):c.114_117dup (p.Glu40fs)
NM_058216.3(RAD51C):c.146-1G>C
NM_058216.3(RAD51C):c.199G>T (p.Glu67Ter)	rs1567785872
NM_058216.3(RAD51C):c.230del (p.Gly77fs)	rs1057519355
NM_058216.3(RAD51C):c.394dup (p.Thr132fs)	rs730881940
NM_058216.3(RAD51C):c.502A>T (p.Arg168Ter)	rs587781490
NM_058216.3(RAD51C):c.525dup (p.Cys176fs)	rs768793789
NM_058216.3(RAD51C):c.68_72dup (p.Val25fs)	rs2047807048
NM_058216.3(RAD51C):c.799C>T (p.Gln267Ter)
NM_058216.3(RAD51C):c.837+1G>C	rs760235677
NM_058216.3(RAD51C):c.907G>T (p.Glu303Ter)	rs2143961266
NM_058216.3(RAD51C):c.93del (p.Phe32fs)	rs730881942
NM_058216.3(RAD51C):c.965+1del
NM_058216.3(RAD51C):c.966-1G>T	rs876658272
NM_058216.3(RAD51C):c.966-2_1026+1del	rs2144044038

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