C3150653[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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Items: 77

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 216798	NM_058216.3(RAD51C):c.3G>T (p.Met1Ile)	RAD51C (M1I)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +3 more	GUncertain significance
Select item 128203	NM_058216.3(RAD51C):c.14C>T (p.Thr5Met)	RAD51C (T5M)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 182841	NM_058216.3(RAD51C):c.29T>G (p.Met10Arg)	RAD51C (M10R)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 184900	NM_058216.3(RAD51C):c.79C>T (p.Leu27=)	RAD51C	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +4 more	GLikely benign
Select item 492389	NM_058216.3(RAD51C):c.88G>T (p.Ala30Ser)	RAD51C (A30S)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +2 more	GUncertain significance
Select item 142534	NM_058216.3(RAD51C):c.97C>T (p.Gln33Ter)	RAD51C (Q33*)	Single nucleotide variant (nonsense +1 more)	Hereditary breast ovarian cancer syndrome +4 more	GPathogenic
Select item 188123	NM_058216.3(RAD51C):c.118G>A (p.Glu40Lys)	RAD51C (E40K)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +3 more	GUncertain significance
Select item 246163	NM_058216.3(RAD51C):c.121G>C (p.Val41Leu)	RAD51C (V41L)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 480520	NM_058216.3(RAD51C):c.146-2A>G	RAD51C	Single nucleotide variant (splice acceptor variant)	Fanconi anemia complementation group O +2 more	GConflicting classifications of pathogenicity
Select item 231616	NM_058216.3(RAD51C):c.158C>G (p.Ser53Cys)	RAD51C (S53C)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 482160	NM_058216.3(RAD51C):c.163G>A (p.Ala55Thr)	RAD51C (A55T)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +3 more	GUncertain significance
Select item 182831	NM_058216.3(RAD51C):c.164C>T (p.Ala55Val)	RAD51C (A55V)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 141999	NM_058216.3(RAD51C):c.186_187del (p.Gln62fs)	RAD51C (Q62fs)	Deletion (frameshift variant +1 more)	Fanconi anemia complementation group O +3 more	GPathogenic
Select item 182832	NM_058216.3(RAD51C):c.200A>G (p.Glu67Gly)	RAD51C (E67G)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +4 more	GUncertain significance
Select item 232705	NM_058216.3(RAD51C):c.211A>T (p.Asn71Tyr)	RAD51C (N71Y)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 480490	NM_058216.3(RAD51C):c.214A>G (p.Lys72Glu)	RAD51C (K72E)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +3 more	GUncertain significance
Select item 182844	NM_058216.3(RAD51C):c.224dup (p.Tyr75Ter)	RAD51C (Y75*)	Duplication (nonsense +1 more)	Hereditary breast ovarian cancer syndrome +4 more	GPathogenic
Select item 241767	NM_058216.3(RAD51C):c.233C>T (p.Thr78Ile)	RAD51C (T78I)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 478609	NM_058216.3(RAD51C):c.250A>T (p.Lys84Ter)	RAD51C (K84*)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +2 more	GPathogenic/Likely pathogenic
Select item 229792	NM_058216.3(RAD51C):c.265G>A (p.Glu89Lys)	RAD51C (E89K)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GUncertain significance
Select item 1517986	NM_058216.3(RAD51C):c.352A>G (p.Met118Val)	RAD51C (M118V)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +1 more	GUncertain significance
Select item 182845	NM_058216.3(RAD51C):c.394dup (p.Thr132fs)	RAD51C (T132fs)	Duplication (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +3 more	GPathogenic
Select item 182835	NM_058216.3(RAD51C):c.404+2T>C	RAD51C	Single nucleotide variant (stop lost +2 more)	not provided +4 more	GPathogenic/Likely pathogenic
Select item 1672481	NM_058216.3(RAD51C):c.404+16C>T	RAD51C	Single nucleotide variant (3 prime UTR variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +1 more	GLikely benign
Select item 141823	NM_058216.3(RAD51C):c.405-1G>C	RAD51C	Single nucleotide variant (splice acceptor variant)	Breast-ovarian cancer, familial, susceptibility to, 3 +3 more	GPathogenic/Likely pathogenic
Select item 128204	NM_058216.3(RAD51C):c.406A>T (p.Met136Leu)	RAD51C (M136L)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome +5 more	GUncertain significance
Select item 6825	NM_058216.3(RAD51C):c.414G>C (p.Leu138Phe)	RAD51C (L138F)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GPathogenic/Likely pathogenic
Select item 142840	NM_058216.3(RAD51C):c.431T>C (p.Ile144Thr)	RAD51C (I144T)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group O +5 more	GConflicting classifications of pathogenicity
Select item 234035	NM_058216.3(RAD51C):c.451G>A (p.Val151Met)	RAD51C (V151M)	Single nucleotide variant (missense variant)	not specified +4 more	GUncertain significance
Select item 570140	NM_058216.3(RAD51C):c.463G>A (p.Ala155Thr)	RAD51C (A155T)	Single nucleotide variant (missense variant)	not provided +5 more	GUncertain significance
Select item 630132	NM_058216.3(RAD51C):c.487A>G (p.Ser163Gly)	RAD51C (S163G)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group O +3 more	GUncertain significance
Select item 188317	NM_058216.3(RAD51C):c.492T>G (p.Phe164Leu)	RAD51C (F164L)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 3 +4 more	GConflicting classifications of pathogenicity
Select item 482171	NM_058216.3(RAD51C):c.493A>G (p.Met165Val)	RAD51C (M165V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 409827	NM_058216.3(RAD51C):c.525dup (p.Cys176fs)	RAD51C (C176fs)	Duplication (frameshift variant)	not provided +3 more	GPathogenic
Select item 184967	NM_058216.3(RAD51C):c.529A>G (p.Ile177Val)	RAD51C (I177V)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 3 +2 more	GUncertain significance
Select item 538795	NM_058216.3(RAD51C):c.537C>T (p.His179=)	RAD51C	Single nucleotide variant (synonymous variant)	Breast-ovarian cancer, familial, susceptibility to, 3 +4 more	GLikely benign
Select item 480501	NM_058216.3(RAD51C):c.546T>G (p.Leu182=)	RAD51C	Single nucleotide variant (synonymous variant)	Fanconi anemia complementation group O +2 more	GLikely benign
Select item 187692	NM_058216.3(RAD51C):c.548T>C (p.Ile183Thr)	RAD51C (I183T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 482173	NM_058216.3(RAD51C):c.556_558dup (p.Lys186dup)	RAD51C	Duplication (inframe_insertion)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 138867	NM_058216.3(RAD51C):c.572-17G>T	RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O +5 more	GBenign/Likely benign
Select item 140849	NM_058216.3(RAD51C):c.577C>T (p.Arg193Ter)	RAD51C (R193*)	Single nucleotide variant (nonsense +1 more)	RAD51C-related disorder +6 more	GPathogenic/Likely pathogenic
Select item 409868	NM_058216.3(RAD51C):c.607A>G (p.Asn203Asp)	LOC129390903, RAD51C (N203D)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 409842	NM_058216.3(RAD51C):c.634C>T (p.Arg212Cys)	LOC129390903, RAD51C (R212C)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +3 more	GUncertain significance
Select item 187633	NM_058216.3(RAD51C):c.635G>A (p.Arg212His)	LOC129390903, RAD51C (R212H)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +5 more	GConflicting classifications of pathogenicity
Select item 186604	NM_058216.3(RAD51C):c.653_654del (p.Glu218fs)	LOC129390903, RAD51C (E218fs)	Microsatellite (frameshift variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GPathogenic/Likely pathogenic
Select item 962088	NM_058216.3(RAD51C):c.674T>C (p.Leu225Pro)	LOC129390903, RAD51C (L225P)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 232379	NM_058216.3(RAD51C):c.696A>T (p.Glu232Asp)	LOC129390903, RAD51C (E232D)	Single nucleotide variant (missense variant +1 more)	RAD51C-related disorder +4 more	GUncertain significance
Select item 142919	NM_058216.3(RAD51C):c.701C>G (p.Ser234Ter)	LOC129390903, RAD51C (S234*)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +3 more	GPathogenic
Select item 216807	NM_058216.3(RAD51C):c.705G>T (p.Lys235Asn)	LOC129390903, RAD51C (K235N)	Single nucleotide variant (missense variant +1 more)	Breast and/or ovarian cancer +4 more	GConflicting classifications of pathogenicity
Select item 230577	NM_058216.3(RAD51C):c.705+1G>A	LOC129390903, RAD51C	Single nucleotide variant (splice donor variant)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic/Likely pathogenic
Select item 378460	NM_058216.3(RAD51C):c.705+14T>C	LOC129390903, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O +3 more	GLikely benign
Select item 631112	NM_058216.3(RAD51C):c.706-2A>C	RAD51C	Single nucleotide variant (splice acceptor variant)	Fanconi anemia complementation group O +2 more	GPathogenic/Likely pathogenic
Select item 128209	NM_058216.3(RAD51C):c.706-2A>G	RAD51C	Single nucleotide variant (splice acceptor variant)	not provided +5 more	GPathogenic/Likely pathogenic
Select item 186364	NM_058216.3(RAD51C):c.709C>T (p.Arg237Ter)	RAD51C (R237*)	Single nucleotide variant (nonsense +1 more)	Hereditary breast ovarian cancer syndrome +4 more	GPathogenic
Select item 219586	NM_058216.3(RAD51C):c.710G>A (p.Arg237Gln)	RAD51C (R237Q)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +4 more	GUncertain significance
Select item 216808	NM_058216.3(RAD51C):c.718A>T (p.Ile240Leu)	RAD51C (I240L)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +5 more	GUncertain significance
Select item 241777	NM_058216.3(RAD51C):c.719T>C (p.Ile240Thr)	RAD51C (I240T)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +4 more	GUncertain significance
Select item 136162	NM_058216.3(RAD51C):c.721G>A (p.Val241Met)	RAD51C (V241M)	Single nucleotide variant (missense variant +1 more)	not specified +5 more	GUncertain significance
Select item 182827	NM_058216.3(RAD51C):c.730A>G (p.Ile244Val)	RAD51C (I244V)	Single nucleotide variant (missense variant +1 more)	Hereditary breast ovarian cancer syndrome +5 more	GUncertain significance
Select item 950391	NM_058216.3(RAD51C):c.740C>T (p.Pro247Leu)	RAD51C (P247L)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +2 more	GUncertain significance
Select item 142453	NM_058216.3(RAD51C):c.772C>T (p.Arg258Cys)	RAD51C (R258C)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +4 more	GUncertain significance
Select item 128210	NM_058216.3(RAD51C):c.784T>G (p.Leu262Val)	RAD51C (L262V)	Single nucleotide variant (missense variant +1 more)	RAD51C-related disorder +6 more	GConflicting classifications of pathogenicity
Select item 827406	NM_058216.3(RAD51C):c.802C>A (p.Gln268Lys)	RAD51C (Q268K)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +2 more	GUncertain significance
Select item 492385	NM_058216.3(RAD51C):c.838-20C>G	RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O +2 more	GLikely benign
Select item 1010953	NM_058216.3(RAD51C):c.904+4G>T	RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O +2 more	GUncertain significance
Select item 1614915	NM_058216.3(RAD51C):c.904+16G>C	RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O +1 more	GLikely benign
Select item 1374071	NM_058216.3(RAD51C):c.904+17A>G	RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O +1 more	GConflicting classifications of pathogenicity
Select item 508893	NM_058216.3(RAD51C):c.905-20A>G	RAD51C	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 492395	NM_058216.3(RAD51C):c.905-19T>C	RAD51C	Single nucleotide variant (intron variant)	not provided +4 more	GBenign/Likely benign
Select item 187133	NM_058216.3(RAD51C):c.923C>G (p.Ala308Gly)	RAD51C (A308G)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +4 more	GUncertain significance
Select item 478782	NM_058216.3(RAD51C):c.966-8T>G	RAD51C	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 3 +1 more	GConflicting classifications of pathogenicity
Select item 490134	NM_058216.3(RAD51C):c.970G>A (p.Ala324Thr)	RAD51C (A324T)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +2 more	GUncertain significance
Select item 128201	NM_058216.3(RAD51C):c.1026+5_1026+7del	RAD51C	Deletion (intron variant)	not provided +5 more	GPathogenic/Likely pathogenic
Select item 185621	NM_058216.3(RAD51C):c.1062A>G (p.Ala354=)	RAD51C	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +4 more	GBenign/Likely benign
Select item 184434	NM_058216.3(RAD51C):c.1089G>A (p.Leu363=)	RAD51C	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +3 more	GLikely benign
Select item 142416	NM_058216.3(RAD51C):c.1096C>T (p.Arg366Trp)	RAD51C (R366W)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +4 more	GUncertain significance
Select item 128202	NM_058216.3(RAD51C):c.1102C>T (p.Arg368Trp)	RAD51C (R368W)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +5 more	GConflicting classifications of pathogenicity

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Items: 77