List of variants in gene RAD51C studied for breast disorder

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: 22

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HGVS	dbSNP	gnomAD frequency
NM_058216.3(RAD51C):c.859A>G (p.Thr287Ala)	rs28363317	0.00653
NM_058216.3(RAD51C):c.376G>A (p.Ala126Thr)	rs61758784	0.00349
NM_058216.3(RAD51C):c.186A>G (p.Gln62=)	rs28363303	0.00322
NM_058216.3(RAD51C):c.790G>A (p.Gly264Ser)	rs147241704	0.00207
NM_058216.3(RAD51C):c.195A>G (p.Arg65=)	rs45511291	0.00105
NM_058216.3(RAD51C):c.784T>G (p.Leu262Val)	rs149331537	0.00014
NM_058216.3(RAD51C):c.506T>C (p.Val169Ala)	rs587780256	0.00009
NM_058216.3(RAD51C):c.870T>A (p.Ile290=)	rs376402418	0.00006
NM_058216.3(RAD51C):c.1062A>G (p.Ala354=)	rs201000407	0.00004
NM_058216.3(RAD51C):c.577C>T (p.Arg193Ter)	rs200293302	0.00004
NM_058216.3(RAD51C):c.1008A>G (p.Thr336=)	rs1057521598	0.00001
NM_058216.3(RAD51C):c.233C>T (p.Thr78Ile)	rs112832782	0.00001
NM_058216.3(RAD51C):c.709C>T (p.Arg237Ter)	rs770637624	0.00001
NM_058216.3(RAD51C):c.772C>T (p.Arg258Cys)	rs587782474	0.00001
NM_058216.3(RAD51C):c.12G>A (p.Lys4=)	rs781166242
NM_058216.3(RAD51C):c.180T>C (p.Thr60=)	rs755092293
NM_058216.3(RAD51C):c.323A>G (p.Asp108Gly)	rs1555593745
NM_058216.3(RAD51C):c.394dup (p.Thr132fs)	rs730881940
NM_058216.3(RAD51C):c.475G>A (p.Asp159Asn)	rs775213492
NM_058216.3(RAD51C):c.81G>A (p.Leu27=)	rs1311969744
NM_058216.3(RAD51C):c.907G>T (p.Glu303Ter)	rs2143961266
NM_058216.3(RAD51C):c.966-2_1026+1del	rs2144044038

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