List of variants in gene RAD51C reported as uncertain significance by Counsyl

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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.146-8A>G	rs201079501	0.00074
NM_058216.3(RAD51C):c.922G>T (p.Ala308Ser)	rs185057307	0.00025
NM_058216.3(RAD51C):c.890T>C (p.Leu297Pro)	rs143026267	0.00017
NM_058216.3(RAD51C):c.784T>G (p.Leu262Val)	rs149331537	0.00014
NM_058216.3(RAD51C):c.431T>C (p.Ile144Thr)	rs28363307	0.00010
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.14C>T (p.Thr5Met)	rs201523760	0.00006
NM_058216.3(RAD51C):c.428A>G (p.Gln143Arg)	rs587780255	0.00006
NM_058216.3(RAD51C):c.492T>G (p.Phe164Leu)	rs573992101	0.00006
NM_058216.3(RAD51C):c.1102C>T (p.Arg368Trp)	rs587780253	0.00003
NM_058216.3(RAD51C):c.77A>T (p.Lys26Met)	rs746026526	0.00003
NM_058216.3(RAD51C):c.537C>A (p.His179Gln)	rs372385738	0.00002
NM_058216.3(RAD51C):c.719T>C (p.Ile240Thr)	rs539341386	0.00002
NM_058216.3(RAD51C):c.746G>A (p.Arg249His)	rs730881925	0.00002
NM_058216.3(RAD51C):c.1109G>A (p.Arg370Gln)	rs373170458	0.00001
NM_058216.3(RAD51C):c.379C>A (p.Pro127Thr)	rs587782222	0.00001
NM_058216.3(RAD51C):c.497T>C (p.Val166Ala)	rs765300465	0.00001
NM_058216.3(RAD51C):c.571+4A>G	rs587780257	0.00001
NM_058216.3(RAD51C):c.772C>T (p.Arg258Cys)	rs587782474	0.00001
NM_058216.3(RAD51C):c.115C>G (p.Leu39Val)	rs759149207
NM_058216.3(RAD51C):c.271C>T (p.Leu91Phe)	rs1555593653
NM_058216.3(RAD51C):c.317C>T (p.Ala106Val)	rs1060502594
NM_058216.3(RAD51C):c.4C>G (p.Arg2Gly)	rs758029117
NM_058216.3(RAD51C):c.520A>G (p.Thr174Ala)	rs864622278
NM_058216.3(RAD51C):c.724G>A (p.Asp242Asn)	rs876659188
NM_058216.3(RAD51C):c.862A>G (p.Thr288Ala)	rs587781574

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