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

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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: 17

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HGVS	dbSNP	gnomAD frequency
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.388G>A (p.Gly130Arg)	rs773293999
NM_058216.3(RAD51C):c.398A>G (p.Gln133Arg)	rs2143727988
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.489T>G (p.Ser163Arg)	rs876659719
NM_058216.3(RAD51C):c.65C>T (p.Ala22Val)	rs2143676047
NM_058216.3(RAD51C):c.752A>G (p.Asp251Gly)	rs2048496443
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.947A>G (p.His316Arg)	rs2143962686
NM_058216.3:c.838_965dup

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