"Sema4, Sema4"[submitter] AND "RAD51D"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 141343	NM_002878.4(RAD51D):c.983C>T (p.Thr328Ile)	RAD51L3-RFFL, RAD51D (T328I +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
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)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 184398	NM_002878.4(RAD51D):c.957G>A (p.Gln319=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GLikely benign
Select item 231010	NM_002878.4(RAD51D):c.945G>A (p.Gly315=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1017562	NM_002878.4(RAD51D):c.938C>G (p.Thr313Ser)	RAD51D, RAD51L3-RFFL (T201S +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GConflicting classifications of pathogenicity
Select item 127896	NM_002878.4(RAD51D):c.932T>A (p.Ile311Asn)	RAD51L3-RFFL, RAD51D (I311N +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +6 more	GConflicting classifications of pathogenicity
Select item 389259	NM_002878.4(RAD51D):c.921G>A (p.Glu307=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
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)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 138877	NM_002878.4(RAD51D):c.904-3C>T	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 182854	NM_002878.4(RAD51D):c.904-11T>A	RAD51L3-RFFL, RAD51D	Single nucleotide variant (intron variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1279943	NM_002878.4(RAD51D):c.904-13C>A	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 4 +2 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)	not specified +3 more	GLikely benign
Select item 1692735	NM_002878.4(RAD51D):c.899G>T (p.Arg300Leu)	RAD51D, RAD51L3-RFFL (R188L +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 239405	NM_002878.4(RAD51D):c.899G>A (p.Arg300Gln)	RAD51D, RAD51L3-RFFL (R300Q +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 185048	NM_002878.4(RAD51D):c.898C>T (p.Arg300Ter)	RAD51D, RAD51L3-RFFL (R300* +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GPathogenic/Likely pathogenic
Select item 410562	NM_002878.4(RAD51D):c.883C>G (p.Leu295Val)	RAD51D, RAD51L3-RFFL (L295V +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 472629	NM_002878.4(RAD51D):c.879G>C (p.Ala293=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 186175	NM_002878.4(RAD51D):c.879G>A (p.Ala293=)	RAD51L3-RFFL, RAD51D	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +3 more	GLikely benign
Select item 187161	NM_002878.4(RAD51D):c.878C>T (p.Ala293Val)	RAD51D, RAD51L3-RFFL (A293V +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +3 more	GConflicting classifications of pathogenicity
Select item 231338	NM_002878.4(RAD51D):c.869G>A (p.Arg290Gln)	RAD51D, RAD51L3-RFFL (R290Q +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 182853	NM_002878.4(RAD51D):c.864C>T (p.Gly288=)	RAD51L3-RFFL, RAD51D	Single nucleotide variant (non-coding transcript variant +1 more)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 245669	NM_002878.4(RAD51D):c.823C>T (p.Arg275Trp)	RAD51D, RAD51L3-RFFL (R275W +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 410552	NM_002878.4(RAD51D):c.803G>A (p.Trp268Ter)	RAD51D, RAD51L3-RFFL (W268* +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +3 more	GPathogenic
Select item 141519	NM_002878.4(RAD51D):c.796C>T (p.Arg266Cys)	RAD51D, RAD51L3-RFFL (R266C +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified +5 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-ovarian cancer, familial, susceptibility to, 4 +3 more	GUncertain significance
Select item 138875	NM_002878.4(RAD51D):c.771C>T (p.Ser257=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 239403	NM_002878.4(RAD51D):c.765G>A (p.Arg255=)	RAD51L3-RFFL, RAD51D	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GLikely benign
Select item 184337	NM_002878.4(RAD51D):c.757C>A (p.Arg253=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (non-coding transcript variant +1 more)	Breast and/or ovarian cancer +3 more	GBenign/Likely benign
Select item 418446	NM_002878.4(RAD51D):c.752T>A (p.Ile251Lys)	RAD51D, RAD51L3-RFFL (I251K +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +2 more	GUncertain significance
Select item 410547	NM_002878.4(RAD51D):c.739G>C (p.Val247Leu)	RAD51D, RAD51L3-RFFL (V247L +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 772503	NM_002878.4(RAD51D):c.739-5T>C	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GConflicting classifications of pathogenicity
Select item 371977	NM_002878.4(RAD51D):c.739-10T>C	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 4 +2 more	GBenign/Likely benign
Select item 187225	NM_002878.4(RAD51D):c.715C>T (p.Arg239Trp)	RAD51D, RAD51L3-RFFL (R239W +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer +3 more	GConflicting classifications of pathogenicity
Select item 127893	NM_002878.4(RAD51D):c.694C>T (p.Arg232Ter)	RAD51D, RAD51L3-RFFL (R232* +2 more)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +5 more	GPathogenic/Likely pathogenic
Select item 1538232	NM_002878.4(RAD51D):c.668-8T>C	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 182852	NM_002878.4(RAD51D):c.666A>G (p.Glu222=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (non-coding transcript variant +1 more)	not specified +3 more	GBenign/Likely benign
Select item 1692734	NM_002878.4(RAD51D):c.652G>A (p.Gly218Ser)	RAD51D, RAD51L3-RFFL (G106S +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 410563	NM_002878.4(RAD51D):c.629C>A (p.Ala210Glu)	RAD51D, RAD51L3-RFFL (A210E +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 141969	NM_002878.4(RAD51D):c.629C>T (p.Ala210Val)	RAD51D, RAD51L3-RFFL (A210V +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary breast ovarian cancer syndrome +4 more	GUncertain significance
Select item 230158	NM_002878.4(RAD51D):c.627T>C (p.Thr209=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely 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 +2 more	GLikely benign
Select item 142102	NM_002878.4(RAD51D):c.620C>T (p.Ser207Leu)	RAD51D, RAD51L3-RFFL (S207L +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary breast ovarian cancer syndrome +4 more	GConflicting classifications of pathogenicity
Select item 1692733	NM_002878.4(RAD51D):c.582T>A (p.Thr194=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 492433	NM_002878.4(RAD51D):c.582T>C (p.Thr194=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GLikely benign
Select item 1692732	NM_002878.4(RAD51D):c.576+5del	RAD51D, RAD51L3-RFFL	Deletion (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1692731	NM_002878.4(RAD51D):c.576+3G>C	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1692730	NM_002878.4(RAD51D):c.576+1_576+2insC	RAD51D, RAD51L3-RFFL	Insertion (splice donor variant)	Hereditary cancer-predisposing syndrome	GLikely pathogenic
Select item 127892	NM_002878.4(RAD51D):c.568G>A (p.Ala190Thr)	RAD51D, RAD51L3-RFFL (A190T +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 30285	NM_002878.4(RAD51D):c.556C>T (p.Arg186Ter)	RAD51D, RAD51L3-RFFL (R186* +2 more)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +3 more	GPathogenic
Select item 142754	NM_002878.4(RAD51D):c.547C>T (p.Gln183Ter)	RAD51D, RAD51L3-RFFL (Q183* +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic/Likely pathogenic
Select item 127891	NM_002878.4(RAD51D):c.493C>T (p.Arg165Trp)	RAD51D, RAD51L3-RFFL (R165W +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +4 more	GUncertain significance
Select item 1692729	NM_002878.4(RAD51D):c.481-2A>G	RAD51D, RAD51L3-RFFL	Single nucleotide variant (splice acceptor variant)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GLikely pathogenic
Select item 231752	NM_002878.4(RAD51D):c.481-4T>G	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 138871	NM_002878.4(RAD51D):c.481-7G>A	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +4 more	GBenign/Likely benign
Select item 379333	NM_002878.4(RAD51D):c.481-11C>T	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 4 +2 more	GLikely benign
Select item 231972	NM_002878.4(RAD51D):c.442C>T (p.Gln148Ter)	RAD51L3-RFFL, RAD51D (Q148* +1 more)	Single nucleotide variant (nonsense +2 more)	Hereditary cancer-predisposing syndrome +3 more	GPathogenic/Likely pathogenic
Select item 187149	NM_002878.4(RAD51D):c.434G>A (p.Arg145His)	RAD51L3-RFFL, RAD51D (R145H +1 more)	Single nucleotide variant (missense variant +2 more)	not provided +2 more	GUncertain significance
Select item 141609	NM_002878.4(RAD51D):c.431C>T (p.Ser144Phe)	RAD51D, RAD51L3-RFFL (S144F +1 more)	Single nucleotide variant (missense variant +2 more)	not provided +4 more	GUncertain significance
Select item 182858	NM_002878.4(RAD51D):c.412A>G (p.Asn138Asp)	RAD51L3-RFFL, RAD51D (N138D +1 more)	Single nucleotide variant (missense variant +2 more)	not specified +3 more	GUncertain significance
Select item 185178	NM_002878.4(RAD51D):c.394G>A (p.Val132Ile)	RAD51D, RAD51L3-RFFL (V132I +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 410554	NM_002878.4(RAD51D):c.392A>G (p.Asn131Ser)	RAD51D, RAD51L3-RFFL (N131S +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1063705	NM_002878.4(RAD51D):c.365C>A (p.Ala122Glu)	RAD51D, RAD51L3-RFFL (A122E +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 182840	NM_002878.4(RAD51D):c.363del (p.Ala122fs)	RAD51D, RAD51L3-RFFL (A122fs +1 more)	Deletion (frameshift variant +2 more)	Hereditary breast ovarian cancer syndrome +3 more	GPathogenic/Likely pathogenic
Select item 234195	NM_002878.4(RAD51D):c.356G>A (p.Cys119Tyr)	RAD51L3-RFFL, RAD51D (C119Y +1 more)	Single nucleotide variant (missense variant +2 more)	not specified +3 more	GUncertain significance
Select item 182856	NM_002878.4(RAD51D):c.355T>C (p.Cys119Arg)	RAD51D, RAD51L3-RFFL (C119R +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary breast ovarian cancer syndrome +5 more	GConflicting classifications of pathogenicity
Select item 184247	NM_002878.4(RAD51D):c.349T>A (p.Cys117Ser)	RAD51D, RAD51L3-RFFL (C117S +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 492427	NM_002878.4(RAD51D):c.346-4C>G	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GConflicting classifications of pathogenicity
Select item 416203	NM_002878.4(RAD51D):c.346-10C>T	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1692728	NM_002878.4(RAD51D):c.346-12C>T	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 492425	NM_002878.4(RAD51D):c.345+6T>C	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GConflicting classifications of pathogenicity
Select item 472599	NM_002878.4(RAD51D):c.343C>T (p.Gln115Ter)	RAD51D, RAD51L3-RFFL (Q115* +1 more)	Single nucleotide variant (nonsense +2 more)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic
Select item 185853	NM_002878.4(RAD51D):c.339A>C (p.Lys113Asn)	RAD51D, RAD51L3-RFFL (K113N +1 more)	Single nucleotide variant (missense variant +2 more)	not provided +2 more	GUncertain significance
Select item 472598	NM_002878.4(RAD51D):c.333C>T (p.Ser111=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +2 more)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 187017	NM_002878.4(RAD51D):c.332G>A (p.Ser111Asn)	RAD51D, RAD51L3-RFFL (S111N +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1692727	NM_002878.4(RAD51D):c.308C>G (p.Thr103Ser)	RAD51D, RAD51L3-RFFL (T103S +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 239394	NM_002878.4(RAD51D):c.270_271dup (p.Lys91fs)	RAD51D, RAD51L3-RFFL (K111fs +1 more)	Duplication (frameshift variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GPathogenic/Likely pathogenic
Select item 548740	NM_002878.4(RAD51D):c.263+1612del	RAD51D, RAD51L3-RFFL (D98fs)	Deletion (frameshift variant +1 more)	RAD51D-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 138879	NM_002878.4(RAD51D):c.263+1588A>G	RAD51D, RAD51L3-RFFL (D90G)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GBenign/Likely benign
Select item 384514	NM_002878.4(RAD51D):c.263+7G>A	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	not provided +3 more	GLikely benign
Select item 138874	NM_002878.4(RAD51D):c.216C>T (p.Tyr72=)	RAD51L3-RFFL, RAD51D	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GBenign/Likely benign
Select item 127885	NM_002878.4(RAD51D):c.208G>A (p.Asp70Asn)	RAD51D, RAD51L3-RFFL (D70N)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +3 more	GConflicting classifications of pathogenicity
Select item 410548	NM_002878.4(RAD51D):c.202G>A (p.Gly68Ser)	RAD51D, RAD51L3-RFFL (G68S)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GUncertain significance
Select item 184496	NM_002878.4(RAD51D):c.198G>T (p.Val66=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +3 more	GBenign/Likely benign
Select item 141578	NM_002878.4(RAD51D):c.196G>A (p.Val66Met)	RAD51D, RAD51L3-RFFL (V66M)	Single nucleotide variant (missense variant +1 more)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 230698	NM_002878.4(RAD51D):c.195C>T (p.Pro65=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GLikely benign
Select item 185036	NM_002878.4(RAD51D):c.185C>T (p.Ser62Leu)	RAD51D, RAD51L3-RFFL (S62L)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GUncertain significance
Select item 186357	NM_002878.4(RAD51D):c.171G>A (p.Leu57=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 230266	NM_002878.4(RAD51D):c.164G>A (p.Arg55Gln)	RAD51D, RAD51L3-RFFL (R55Q)	Single nucleotide variant (missense variant +1 more)	not specified +4 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)	Breast-ovarian cancer, familial, susceptibility to, 4 +4 more	GConflicting classifications of pathogenicity
Select item 141453	NM_002878.4(RAD51D):c.145-4G>A	RAD51L3-RFFL, RAD51D	Single nucleotide variant (intron variant)	Breast and/or ovarian cancer +4 more	GConflicting classifications of pathogenicity
Select item 380544	NM_002878.4(RAD51D):c.145-13G>T	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 4 +3 more	GConflicting classifications of pathogenicity
Select item 127882	NM_002878.4(RAD51D):c.137C>G (p.Ser46Cys)	RAD51D, RAD51L3-RFFL (S46C)	Single nucleotide variant (missense variant +1 more)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 826759	NM_002878.4(RAD51D):c.69C>T (p.His23=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GLikely benign
Select item 482186	NM_002878.4(RAD51D):c.56T>C (p.Leu19Pro)	RAD51D, RAD51L3-RFFL (L19P)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 232535	NM_002878.4(RAD51D):c.53A>G (p.Gln18Arg)	RAD51D, RAD51L3-RFFL (Q18R)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +3 more	GConflicting classifications of pathogenicity
Select item 184815	NM_002878.4(RAD51D):c.39C>G (p.Thr13=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +2 more	GLikely benign
Select item 422517	NM_002878.4(RAD51D):c.38C>T (p.Thr13Ile)	RAD51D, RAD51L3-RFFL (T13I)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GUncertain significance
Select item 231681	NM_002878.4(RAD51D):c.33C>T (p.Gly11=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GLikely benign
Select item 185973	NM_002878.4(RAD51D):c.27C>T (p.Cys9=)	RAD51D, RAD51L3-RFFL	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +2 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-predisposing syndrome +5 more	GConflicting classifications of pathogenicity

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