List of variants in gene RAD51C studied for carcinoma

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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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.431T>C (p.Ile144Thr)	rs28363307	0.00010
NM_058216.3(RAD51C):c.577C>T (p.Arg193Ter)	rs200293302	0.00004
NM_058216.3(RAD51C):c.709C>T (p.Arg237Ter)	rs770637624	0.00001
NM_058216.3(RAD51C):c.12G>A (p.Lys4=)	rs781166242
NM_058216.3(RAD51C):c.146-4_146-2del	rs1555593450
NM_058216.3(RAD51C):c.180T>C (p.Thr60=)	rs755092293
NM_058216.3(RAD51C):c.394A>C (p.Thr132Pro)	rs2047959481
NM_058216.3(RAD51C):c.502A>T (p.Arg168Ter)	rs587781490
NM_058216.3(RAD51C):c.907G>T (p.Glu303Ter)	rs2143961266

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