List of variants in gene RAD51C reported as uncertain significance for Hereditary breast ovarian cancer syndrome

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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: 27

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HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.790G>A (p.Gly264Ser)	rs147241704	0.00207
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.1102C>T (p.Arg368Trp)	rs587780253	0.00003
NM_058216.3(RAD51C):c.7G>A (p.Gly3Arg)	rs376403182	0.00003
NM_058216.3(RAD51C):c.719T>C (p.Ile240Thr)	rs539341386	0.00002
NM_058216.3(RAD51C):c.1051G>A (p.Val351Ile)	rs1160208500	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.730A>G (p.Ile244Val)	rs199886026	0.00001
NM_058216.3(RAD51C):c.935G>A (p.Arg312Gln)	rs779834376	0.00001
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.20G>C (p.Arg7Pro)	rs892567748
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.386T>C (p.Val129Ala)	rs876660641
NM_058216.3(RAD51C):c.3G>C (p.Met1Ile)	rs769053886
NM_058216.3(RAD51C):c.493A>G (p.Met165Val)	rs1555594766
NM_058216.3(RAD51C):c.572-11del	rs587780258
NM_058216.3(RAD51C):c.68T>G (p.Val23Gly)	rs2047807604
NM_058216.3(RAD51C):c.724G>A (p.Asp242Asn)	rs876659188
NM_058216.3(RAD51C):c.760G>T (p.Asp254Tyr)	rs1567799662
NM_058216.3(RAD51C):c.904G>A (p.Gly302Arg)	rs1555602158

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