"Clinical Genetics Laboratory, Department of Pathology, Netherlands Ca - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 127896	NM_002878.4(RAD51D):c.932T>A (p.Ile311Asn)	RAD51D, RAD51L3-RFFL (I311N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +6 more	GConflicting classifications of pathogenicity
Select item 676537	NM_002878.4(RAD51D):c.903+53C>T	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 138873	NM_002878.4(RAD51D):c.698A>G (p.Glu233Gly)	RAD51D, RAD51L3-RFFL (E233G +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified +3 more	GBenign/Likely benign
Select item 138872	NM_002878.4(RAD51D):c.695G>A (p.Arg232Gln)	RAD51D, RAD51L3-RFFL (R232Q +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast and/or ovarian cancer +4 more	GBenign/Likely benign
Select item 142159	NM_002878.4(RAD51D):c.494G>A (p.Arg165Gln)	RAD51L3-RFFL, RAD51D (R165Q +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified +3 more	GBenign
Select item 183785	NM_002878.4(RAD51D):c.234C>T (p.Ser78=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GBenign

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