"PreventionGenetics, part of Exact Sciences"[submitter] AND "RAD51D"[g - ClinVar

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Items: 53

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 141343	NM_002878.4(RAD51D):c.983C>T (p.Thr328Ile)	RAD51D, RAD51L3-RFFL (T328I +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 187753	NM_002878.4(RAD51D):c.979C>T (p.Gln327Ter)	RAD51D, RAD51L3-RFFL (Q327* +2 more)	Single nucleotide variant (nonsense +1 more)	not provided +2 more	GUncertain significance
Select item 127898	NM_002878.4(RAD51D):c.973G>A (p.Gly325Ser)	RAD51D, RAD51L3-RFFL (G325S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 127895	NM_002878.4(RAD51D):c.919G>A (p.Glu307Lys)	RAD51D, RAD51L3-RFFL (E307K +2 more)	Single nucleotide variant (missense variant +1 more)	Breast and/or ovarian cancer +5 more	GConflicting classifications of pathogenicity
Select item 138877	NM_002878.4(RAD51D):c.904-3C>T	RAD51L3-RFFL, RAD51D	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 185315	NM_002878.4(RAD51D):c.900A>G (p.Arg300=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +4 more	GLikely benign
Select item 187161	NM_002878.4(RAD51D):c.878C>T (p.Ala293Val)	RAD51L3-RFFL, RAD51D (A293V +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +4 more	GConflicting classifications of pathogenicity
Select item 138876	NM_002878.4(RAD51D):c.873C>T (p.Arg291=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GBenign/Likely benign
Select item 182853	NM_002878.4(RAD51D):c.864C>T (p.Gly288=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +4 more	GConflicting classifications of pathogenicity
Select item 568973	NM_002878.4(RAD51D):c.833T>C (p.Leu278Pro)	RAD51D, RAD51L3-RFFL (L278P +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	RAD51D-related disorder +2 more	GUncertain significance
Select item 141519	NM_002878.4(RAD51D):c.796C>T (p.Arg266Cys)	RAD51L3-RFFL, RAD51D (R266C +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified +6 more	GConflicting classifications of pathogenicity
Select item 142125	NM_002878.4(RAD51D):c.793G>A (p.Gly265Arg)	RAD51D, RAD51L3-RFFL (G265R +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast and/or ovarian cancer +3 more	GUncertain significance
Select item 239403	NM_002878.4(RAD51D):c.765G>A (p.Arg255=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +4 more	GLikely benign
Select item 410568	NM_002878.4(RAD51D):c.758G>A (p.Arg253Gln)	RAD51D, RAD51L3-RFFL (R253Q +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +2 more	GUncertain significance
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)	Breast-ovarian cancer, familial, susceptibility to, 4 +3 more	GBenign/Likely benign
Select item 138872	NM_002878.4(RAD51D):c.695G>A (p.Arg232Gln)	RAD51L3-RFFL, RAD51D (R232Q +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +4 more	GBenign/Likely benign
Select item 472619	NM_002878.4(RAD51D):c.680T>C (p.Met227Thr)	RAD51D, RAD51L3-RFFL (M227T +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +2 more	GUncertain significance
Select item 380537	NM_002878.4(RAD51D):c.667+20C>T	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	not specified +3 more	GLikely benign
Select item 182852	NM_002878.4(RAD51D):c.666A>G (p.Glu222=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 185908	NM_002878.4(RAD51D):c.621G>T (p.Ser207=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GLikely benign
Select item 182860	NM_002878.4(RAD51D):c.607G>A (p.Val203Met)	RAD51D, RAD51L3-RFFL (V203M +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +4 more	GUncertain significance
Select item 578475	NM_002878.4(RAD51D):c.598G>A (p.Val200Met)	RAD51D, RAD51L3-RFFL (V200M +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +2 more	GUncertain significance
Select item 388072	NM_002878.4(RAD51D):c.576+19C>T	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GLikely benign
Select item 30285	NM_002878.4(RAD51D):c.556C>T (p.Arg186Ter)	RAD51D, RAD51L3-RFFL (R186* +2 more)	Single nucleotide variant (nonsense +1 more)	Hereditary cancer-predisposing syndrome +3 more	GPathogenic
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 239398	NM_002878.4(RAD51D):c.481-8C>T	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 4 +4 more	GConflicting classifications of pathogenicity
Select item 187149	NM_002878.4(RAD51D):c.434G>A (p.Arg145His)	RAD51D, RAD51L3-RFFL (R145H +1 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +3 more	GUncertain significance
Select item 1586965	NM_002878.4(RAD51D):c.348A>T (p.Val116=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +2 more	GLikely benign
Select item 416203	NM_002878.4(RAD51D):c.346-10C>T	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 2779136	NM_002878.4(RAD51D):c.342T>C (p.Thr114=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +2 more)	RAD51D-related disorder +1 more	GLikely benign
Select item 2630681	NM_002878.4(RAD51D):c.340dup (p.Thr114fs)	RAD51D, RAD51L3-RFFL (T114fs +1 more)	Duplication (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GPathogenic
Select item 472597	NM_002878.4(RAD51D):c.307A>G (p.Thr103Ala)	RAD51L3-RFFL, RAD51D (T103A +1 more)	Single nucleotide variant (missense variant +2 more)	RAD51D-related disorder +3 more	GUncertain significance
Select item 3052341	NM_002878.4(RAD51D):c.263+1628G>A	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	RAD51D-related disorder	GLikely benign
Select item 548740	NM_002878.4(RAD51D):c.263+1612del	RAD51D, RAD51L3-RFFL (D98fs)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +2 more	GConflicting classifications of pathogenicity
Select item 138880	NM_002878.4(RAD51D):c.263+1605G>A	RAD51L3-RFFL, RAD51D (A96T)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +3 more	GBenign/Likely benign
Select item 138879	NM_002878.4(RAD51D):c.263+1588A>G	RAD51D, RAD51L3-RFFL (D90G)	Single nucleotide variant (missense variant +1 more)	RAD51D-related disorder +4 more	GBenign/Likely benign
Select item 138878	NM_002878.4(RAD51D):c.263+1570T>A	RAD51D, RAD51L3-RFFL (L84H)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +2 more	GBenign/Likely benign
Select item 2635399	NM_002878.4(RAD51D):c.263+1558A>G	RAD51D, RAD51L3-RFFL (K80R)	Single nucleotide variant (missense variant +1 more)	RAD51D-related disorder	GUncertain significance
Select item 371900	NM_002878.4(RAD51D):c.263+1509C>T	RAD51D, RAD51L3-RFFL (P64S)	Single nucleotide variant (missense variant +1 more)	RAD51D-related disorder +1 more	GLikely benign
Select item 3034391	NM_002878.4(RAD51D):c.263+1475G>A	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	RAD51D-related disorder	GLikely benign
Select item 492414	NM_002878.4(RAD51D):c.263+1474C>T	RAD51D, RAD51L3-RFFL (A52V)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GBenign/Likely benign
Select item 480542	NM_002878.4(RAD51D):c.263+1G>A	RAD51D, RAD51L3-RFFL	Single nucleotide variant (splice donor variant +1 more)	RAD51D-related disorder +3 more	GConflicting classifications of pathogenicity
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
Select item 141578	NM_002878.4(RAD51D):c.196G>A (p.Val66Met)	RAD51D, RAD51L3-RFFL (V66M)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +6 more	GConflicting classifications of pathogenicity
Select item 1057566	NM_002878.4(RAD51D):c.190T>C (p.Phe64Leu)	RAD51D, RAD51L3-RFFL (F64L)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +2 more	GUncertain significance
Select item 127883	NM_002878.4(RAD51D):c.146C>T (p.Ala49Val)	RAD51D, RAD51L3-RFFL (A49V)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 141453	NM_002878.4(RAD51D):c.145-4G>A	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	Breast and/or ovarian cancer +5 more	GConflicting classifications of pathogenicity
Select item 480525	NM_002878.4(RAD51D):c.136T>C (p.Ser46Pro)	RAD51D, RAD51L3-RFFL (S46P)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 185380	NM_002878.4(RAD51D):c.108G>A (p.Leu36=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +2 more	GLikely benign
Select item 184815	NM_002878.4(RAD51D):c.39C>G (p.Thr13=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GLikely benign
Select item 127886	NM_002878.4(RAD51D):c.26G>C (p.Cys9Ser)	RAD51L3-RFFL, RAD51D (C9S)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer +6 more	GConflicting classifications of pathogenicity
Select item 186752	NM_002878.4(RAD51D):c.12C>G (p.Leu4=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GLikely benign
Select item 492404	NM_002878.4(RAD51D):c.-7G>A	RAD51L3-RFFL, RAD51D	Single nucleotide variant (5 prime UTR variant +1 more)	not specified +2 more	GConflicting classifications of pathogenicity

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Items: 53