"Baylor Genetics"[submitter] AND "RAD51D"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 472632	NM_002878.4(RAD51D):c.955_959dup (p.Ala321fs)	RAD51L3-RFFL, RAD51D (A209fs +2 more)	Microsatellite (frameshift variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 480539	NM_002878.4(RAD51D):c.959G>T (p.Ser320Ile)	RAD51D, RAD51L3-RFFL (S320I +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 193645	NM_002878.4(RAD51D):c.955C>T (p.Gln319Ter)	RAD51L3-RFFL, RAD51D (Q319* +2 more)	Single nucleotide variant (nonsense +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 230736	NM_002878.4(RAD51D):c.952G>A (p.Glu318Lys)	RAD51D, RAD51L3-RFFL (E318K +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 231621	NM_002878.4(RAD51D):c.944G>T (p.Gly315Val)	RAD51D, RAD51L3-RFFL (G315V +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 185649	NM_002878.4(RAD51D):c.943G>C (p.Gly315Arg)	RAD51D, RAD51L3-RFFL (G315R +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2678188	NM_002878.4(RAD51D):c.934G>T (p.Gly312Trp)	RAD51D, RAD51L3-RFFL (G200W +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 141707	NM_002878.4(RAD51D):c.911G>A (p.Gly304Asp)	RAD51D, RAD51L3-RFFL (G304D +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +3 more	GUncertain significance
Select item 232482	NM_002878.4(RAD51D):c.910G>T (p.Gly304Cys)	RAD51D, RAD51L3-RFFL (G304C +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 823000	NM_002878.4(RAD51D):c.908C>T (p.Thr303Ile)	RAD51D, RAD51L3-RFFL (T323I +2 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GUncertain significance
Select item 472631	NM_002878.4(RAD51D):c.904-2A>T	RAD51D, RAD51L3-RFFL	Single nucleotide variant (splice acceptor variant)	Hereditary breast ovarian cancer syndrome +2 more	GConflicting classifications of pathogenicity
Select item 410561	NM_002878.4(RAD51D):c.901C>T (p.Gln301Ter)	RAD51L3-RFFL, RAD51D (Q301* +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GLikely pathogenic
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 185528	NM_002878.4(RAD51D):c.898del (p.Arg300fs)	RAD51L3-RFFL, RAD51D (R320fs +1 more)	Deletion (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic/Likely pathogenic
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 182865	NM_002878.4(RAD51D):c.872G>A (p.Arg291His)	RAD51D, RAD51L3-RFFL (R291H +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 231161	NM_002878.4(RAD51D):c.871C>T (p.Arg291Cys)	RAD51D, RAD51L3-RFFL (R291C +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 187277	NM_002878.4(RAD51D):c.868C>T (p.Arg290Trp)	RAD51D, RAD51L3-RFFL (R290W +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 2574360	NM_002878.4(RAD51D):c.836A>G (p.Asp279Gly)	RAD51D, RAD51L3-RFFL (D167G +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GUncertain significance
Select item 568973	NM_002878.4(RAD51D):c.833T>C (p.Leu278Pro)	RAD51L3-RFFL, RAD51D (L278P +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 185774	NM_002878.4(RAD51D):c.824G>A (p.Arg275Gln)	RAD51D, RAD51L3-RFFL (R275Q +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
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 234037	NM_002878.4(RAD51D):c.802T>A (p.Trp268Arg)	RAD51D, RAD51L3-RFFL (W268R +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +3 more	GUncertain significance
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 492444	NM_002878.4(RAD51D):c.784C>A (p.Pro262Thr)	RAD51D, RAD51L3-RFFL (P262T +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +2 more	GUncertain significance
Select item 421303	NM_002878.4(RAD51D):c.772_778del (p.Gly258fs)	RAD51D, RAD51L3-RFFL (G146fs +2 more)	Deletion (non-coding transcript variant +1 more)	not provided +2 more	GPathogenic/Likely pathogenic
Select item 186803	NM_002878.4(RAD51D):c.772G>A (p.Gly258Arg)	RAD51L3-RFFL, RAD51D (G258R +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +2 more	GConflicting classifications of pathogenicity
Select item 628572	NM_002878.4(RAD51D):c.769A>G (p.Ser257Gly)	RAD51D, RAD51L3-RFFL (S257G +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 482193	NM_002878.4(RAD51D):c.764G>A (p.Arg255Lys)	RAD51D, RAD51L3-RFFL (R255K +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 30288	NM_002878.4(RAD51D):c.757C>T (p.Arg253Ter)	RAD51D, RAD51L3-RFFL (R253* +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 949331	NM_002878.4(RAD51D):c.754A>C (p.Thr252Pro)	RAD51D, RAD51L3-RFFL (T272P +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
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 127894	NM_002878.4(RAD51D):c.748del (p.His250fs)	RAD51D, RAD51L3-RFFL (H138fs +2 more)	Deletion (non-coding transcript variant +1 more)	Breast and/or ovarian cancer +4 more	GPathogenic/Likely pathogenic
Select item 182862	NM_002878.4(RAD51D):c.745A>G (p.Asn249Asp)	RAD51L3-RFFL, RAD51D (N249D +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +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 480532	NM_002878.4(RAD51D):c.739-1G>A	RAD51D, RAD51L3-RFFL	Single nucleotide variant (splice acceptor variant)	not provided +2 more	GLikely pathogenic
Select item 2678193	NM_002878.4(RAD51D):c.739-18A>G	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 492442	NM_002878.4(RAD51D):c.738+14C>T	RAD51L3-RFFL, RAD51D	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 480880	NM_002878.4(RAD51D):c.738+4A>G	RAD51D, RAD51L3-RFFL	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2018478	NM_002878.4(RAD51D):c.738+1G>T	RAD51D, RAD51L3-RFFL	Single nucleotide variant (splice donor variant)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GLikely pathogenic
Select item 480527	NM_002878.4(RAD51D):c.726C>T (p.Gly242=)	RAD51L3-RFFL, RAD51D	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 230770	NM_002878.4(RAD51D):c.725G>T (p.Gly242Val)	RAD51D, RAD51L3-RFFL (G242V +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GUncertain significance
Select item 229883	NM_002878.4(RAD51D):c.716G>A (p.Arg239Gln)	RAD51D, RAD51L3-RFFL (R239Q +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +4 more	GUncertain significance
Select item 472620	NM_002878.4(RAD51D):c.715C>G (p.Arg239Gly)	RAD51L3-RFFL, RAD51D (R239G +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 141910	NM_002878.4(RAD51D):c.712G>A (p.Ala238Thr)	RAD51D, RAD51L3-RFFL (A238T +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +2 more	GUncertain significance
Select item 1506962	NM_002878.4(RAD51D):c.694_697dup (p.Glu233fs)	RAD51D, RAD51L3-RFFL (E121fs +2 more)	Duplication (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic/Likely pathogenic
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 480531	NM_002878.4(RAD51D):c.691G>T (p.Ala231Ser)	RAD51D, RAD51L3-RFFL (A231S +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
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 629951	NM_002878.4(RAD51D):c.671T>A (p.Leu224Ter)	RAD51D, RAD51L3-RFFL (L224* +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GPathogenic/Likely pathogenic
Select item 568391	NM_002878.4(RAD51D):c.668-2A>C	RAD51D, RAD51L3-RFFL	Single nucleotide variant (splice acceptor variant)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GLikely pathogenic
Select item 3240257	NM_002878.4(RAD51D):c.661A>T (p.Arg221Trp)	RAD51L3-RFFL, RAD51D (R109W +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 3240255	NM_002878.4(RAD51D):c.661A>G (p.Arg221Gly)	RAD51D, RAD51L3-RFFL (R109G +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 141143	NM_002878.4(RAD51D):c.649_655delinsTGAGGTT (p.Gly217_Gln219delinsTer)	RAD51D, RAD51L3-RFFL	Indel (non-coding transcript variant +1 more)	Hereditary breast ovarian cancer syndrome +2 more	GPathogenic
Select item 492434	NM_002878.4(RAD51D):c.641dup (p.Leu215fs)	RAD51D, RAD51L3-RFFL (L235fs +2 more)	Duplication (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GLikely pathogenic
Select item 574602	NM_002878.4(RAD51D):c.641C>T (p.Pro214Leu)	RAD51D, RAD51L3-RFFL (P214L +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 182861	NM_002878.4(RAD51D):c.634G>A (p.Val212Ile)	RAD51L3-RFFL, RAD51D (V212I +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +2 more	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 484765	NM_002878.4(RAD51D):c.625A>C (p.Thr209Pro)	RAD51D, RAD51L3-RFFL (T209P +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GUncertain significance
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 229719	NM_002878.4(RAD51D):c.619T>C (p.Ser207Pro)	RAD51L3-RFFL, RAD51D (S207P +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 182850	NM_002878.4(RAD51D):c.603GGT[2] (p.Val205del)	RAD51L3-RFFL, RAD51D (V205del +2 more)	Microsatellite (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
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)	Hereditary breast ovarian cancer syndrome +3 more	GUncertain significance
Select item 848749	NM_002878.4(RAD51D):c.584G>A (p.Gly195Asp)	RAD51D, RAD51L3-RFFL (G195D +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GUncertain significance
Select item 482184	NM_002878.4(RAD51D):c.577-2A>G	RAD51D, RAD51L3-RFFL	Single nucleotide variant (splice acceptor variant)	Hereditary cancer-predisposing syndrome +3 more	GPathogenic/Likely pathogenic
Select item 641144	NM_002878.4(RAD51D):c.576+1G>T	RAD51D, RAD51L3-RFFL	Single nucleotide variant (splice donor variant)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 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 1443477	NM_002878.4(RAD51D):c.553C>T (p.Leu185Phe)	RAD51D, RAD51L3-RFFL (L205F +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 187314	NM_002878.4(RAD51D):c.550G>A (p.Glu184Lys)	RAD51L3-RFFL, RAD51D (E184K +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +3 more	GUncertain significance
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 230636	NM_002878.4(RAD51D):c.541G>A (p.Val181Met)	RAD51D, RAD51L3-RFFL (V181M +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +2 more	GUncertain significance
Select item 2575698	NM_002878.4(RAD51D):c.533T>C (p.Met178Thr)	RAD51D, RAD51L3-RFFL (M178T +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GUncertain significance
Select item 185143	NM_002878.4(RAD51D):c.530A>T (p.Gln177Leu)	RAD51D, RAD51L3-RFFL (Q177L +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GUncertain significance
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 1743291	NM_002878.4(RAD51D):c.481-1G>T	RAD51D, RAD51L3-RFFL	Single nucleotide variant (splice acceptor variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 186269	NM_002878.4(RAD51D):c.473_480+1del	RAD51D, RAD51L3-RFFL	Deletion (splice donor variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 384322	NM_002878.4(RAD51D):c.478C>T (p.Gln160Ter)	RAD51D, RAD51L3-RFFL (Q160* +1 more)	Single nucleotide variant (nonsense +2 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +2 more	GPathogenic
Select item 484775	NM_002878.4(RAD51D):c.463C>T (p.Gln155Ter)	RAD51L3-RFFL, RAD51D (Q155* +1 more)	Single nucleotide variant (nonsense +2 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GPathogenic/Likely pathogenic
Select item 232172	NM_002878.4(RAD51D):c.455C>A (p.Ala152Asp)	RAD51D, RAD51L3-RFFL (A152D +1 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GUncertain significance
Select item 141452	NM_002878.4(RAD51D):c.451C>T (p.Gln151Ter)	RAD51D, RAD51L3-RFFL (Q151* +1 more)	Single nucleotide variant (nonsense +2 more)	Hereditary breast ovarian cancer syndrome +3 more	GPathogenic/Likely pathogenic
Select item 574981	NM_002878.4(RAD51D):c.439C>T (p.Leu147Phe)	RAD51D, RAD51L3-RFFL (L147F +1 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GUncertain significance
Select item 410559	NM_002878.4(RAD51D):c.436C>T (p.Leu146Phe)	RAD51L3-RFFL, RAD51D (L146F +1 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +2 more	GUncertain significance
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 2678191	NM_002878.4(RAD51D):c.432_433del (p.Arg145fs)	RAD51L3-RFFL, RAD51D (R145fs +1 more)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 4	GLikely pathogenic
Select item 231938	NM_002878.4(RAD51D):c.433C>T (p.Arg145Cys)	RAD51D, RAD51L3-RFFL (R145C +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +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 186683	NM_002878.4(RAD51D):c.422T>C (p.Leu141Pro)	RAD51D, RAD51L3-RFFL (L141P +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 182851	NM_002878.4(RAD51D):c.419G>A (p.Gly140Glu)	RAD51D, RAD51L3-RFFL (G140E +1 more)	Single nucleotide variant (missense variant +2 more)	not specified +3 more	GUncertain significance
Select item 490140	NM_002878.4(RAD51D):c.415G>A (p.Gly139Arg)	RAD51L3-RFFL, RAD51D (G139R +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +1 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 127888	NM_002878.4(RAD51D):c.412A>C (p.Asn138His)	RAD51L3-RFFL, RAD51D (N138H +1 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +3 more	GConflicting classifications of pathogenicity
Select item 2678185	NM_002878.4(RAD51D):c.410C>A (p.Ser137Tyr)	RAD51D, RAD51L3-RFFL (S137Y +1 more)	Single nucleotide variant (intron variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 4 +1 more	GUncertain significance
Select item 232305	NM_002878.4(RAD51D):c.407A>G (p.Asp136Gly)	RAD51D, RAD51L3-RFFL (D136G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified +2 more	GUncertain significance
Select item 2678180	NM_002878.4(RAD51D):c.400T>C (p.Tyr134His)	RAD51D, RAD51L3-RFFL (Y134H +1 more)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 4	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

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