Related gene-specific medical variations for Gene (Select 5889) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3256360	NM_058216.3(RAD51C):c.699C>G (p.His233Gln)	LOC129390903, RAD51C (H233Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3243093	NC_000017.10:g.(?_56777232)_(56780574_?)del	RAD51C	Deletion	Fanconi anemia complementation group O	GLikely pathogenic
Select item 3243092	NC_000017.10:g.(?_56809835)_(56811583_?)dup	RAD51C	Duplication	Fanconi anemia complementation group O	GUncertain significance
Select item 3243091	NC_000017.10:g.(?_56798097)_(56801482_?)dup	RAD51C	Duplication	Fanconi anemia complementation group O	GLikely pathogenic
Select item 3243090	NC_000017.10:g.(?_56770005)_(56801481_?)dup	RAD51C	Duplication	Fanconi anemia complementation group O	GUncertain significance
Select item 3243089	NC_000017.10:g.(?_56769986)_(56772560_?)dup	RAD51C	Duplication	Fanconi anemia complementation group O	GUncertain significance
Select item 3243088	NC_000017.10:g.(?_56769986)_(56811583_?)dup	RAD51C	Duplication	Fanconi anemia complementation group O	GUncertain significance
Select item 3243086	NC_000017.10:g.(?_56809825)_(56811583_?)del	RAD51C	Deletion	Fanconi anemia complementation group O	GPathogenic
Select item 3243085	NC_000017.10:g.(?_56801381)_(56811583_?)del	RAD51C	Deletion	Fanconi anemia complementation group O	GLikely pathogenic
Select item 3243084	NC_000017.10:g.(?_56787200)_(56811583_?)del	RAD51C	Deletion	Fanconi anemia complementation group O	GPathogenic
Select item 3243083	NC_000017.10:g.(?_56780537)_(56787371_?)del	RAD51C	Deletion	Fanconi anemia complementation group O	GPathogenic
Select item 3243082	NC_000017.10:g.(?_56770005)_(56787371_?)del	RAD51C	Deletion	Fanconi anemia complementation group O	GPathogenic
Select item 3243081	NC_000017.10:g.(?_56769986)_(56772560_?)del	RAD51C	Deletion	Fanconi anemia complementation group O	GPathogenic
Select item 3243080	NC_000017.10:g.(?_56809825)_(56809925_?)del	RAD51C	Deletion	Fanconi anemia complementation group O	GPathogenic
Select item 3243079	NC_000017.10:g.(?_56780537)_(56780710_?)del	RAD51C	Deletion	Fanconi anemia complementation group O	GPathogenic
Select item 3243078	NC_000017.10:g.(?_56770005)_(56811583_?)del	RAD51C	Deletion	Fanconi anemia complementation group O	GPathogenic
Select item 3243077	NC_000017.10:g.(?_56809835)_(56809915_?)del	RAD51C	Deletion	Fanconi anemia complementation group O	GPathogenic
Select item 3240253	NM_058216.3(RAD51C):c.268C>A (p.Leu90Ile)	RAD51C (L90I)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3	GUncertain significance
Select item 3240252	NM_058216.3(RAD51C):c.843T>G (p.Ile281Met)	RAD51C (I281M)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3	GUncertain significance
Select item 3228946	NM_058216.3(RAD51C):c.145+5C>G	LOC130061310, RAD51C	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3148640	NM_058216.3(RAD51C):c.698del (p.His233fs)	LOC129390903, RAD51C (H233fs)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3	GPathogenic
Select item 3148622	NM_058216.3(RAD51C):c.704_705+21del	LOC129390903, RAD51C	Deletion (splice donor variant)	Breast-ovarian cancer, familial, susceptibility to, 3	GLikely pathogenic
Select item 3148608	NM_058216.3(RAD51C):c.699_702del (p.His233fs)	LOC129390903, RAD51C (H233fs)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3	GPathogenic
Select item 3148407	NM_058216.3(RAD51C):c.656dup (p.Leu219fs)	LOC129390903, RAD51C (L219fs)	Duplication (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3	GPathogenic
Select item 3148354	NM_058216.3(RAD51C):c.616dup (p.Ser206fs)	LOC129390903, RAD51C (S206fs)	Duplication (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3	GPathogenic
Select item 3148029	NM_058216.3(RAD51C):c.630T>A (p.Tyr210Ter)	LOC129390903, RAD51C (Y210*)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3	GPathogenic
Select item 3022684	NM_058216.3(RAD51C):c.145+12T>C	LOC130061310, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O	GLikely benign
Select item 2996399	NM_058216.3(RAD51C):c.145+10C>G	LOC130061310, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O	GLikely benign
Select item 2974391	NM_058216.3(RAD51C):c.637T>C (p.Cys213Arg)	LOC129390903, RAD51C (C213R)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O	GUncertain significance
Select item 2964839	NM_058216.3(RAD51C):c.698A>C (p.His233Pro)	LOC129390903, RAD51C (H233P)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O	GUncertain significance
Select item 2898599	NM_058216.3(RAD51C):c.705+15A>G	LOC129390903, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O	GLikely benign
Select item 2863092	NM_058216.3(RAD51C):c.705+13C>T	LOC129390903, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O	GLikely benign
Select item 2863056	NM_058216.3(RAD51C):c.685T>A (p.Phe229Ile)	LOC129390903, RAD51C (F229I)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O	GUncertain significance
Select item 2847263	NM_058216.3(RAD51C):c.601C>T (p.Leu201Phe)	LOC129390903, RAD51C (L201F)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O	GUncertain significance
Select item 2824103	NM_058216.3(RAD51C):c.663A>C (p.Ala221=)	LOC129390903, RAD51C	Single nucleotide variant (synonymous variant +1 more)	Fanconi anemia complementation group O	GLikely benign
Select item 2821551	NM_058216.3(RAD51C):c.705+6A>C	LOC129390903, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O	GUncertain significance
Select item 2787503	NM_058216.3(RAD51C):c.648C>T (p.Tyr216=)	LOC129390903, RAD51C	Single nucleotide variant (synonymous variant +1 more)	Fanconi anemia complementation group O	GLikely benign
Select item 2774198	NM_058216.3(RAD51C):c.645C>T (p.Asp215=)	LOC129390903, RAD51C	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2774190	NM_058216.3(RAD51C):c.145+6G>A	LOC130061310, RAD51C	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 2758307	NM_058216.3(RAD51C):c.145+4dup	LOC130061310, RAD51C	Duplication (intron variant)	Fanconi anemia complementation group O	GUncertain significance
Select item 2739763	NM_058216.3(RAD51C):c.145+10C>T	LOC130061310, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O	GLikely benign
Select item 2738799	NM_058216.3(RAD51C):c.659T>C (p.Leu220Pro)	LOC129390903, RAD51C (L220P)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2719449	NM_058216.3(RAD51C):c.145+19A>G	LOC130061310, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O	GLikely benign
Select item 2713370	NM_058216.3(RAD51C):c.649A>C (p.Thr217Pro)	LOC129390903, RAD51C (T217P)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O	GUncertain significance
Select item 2710410	NM_058216.3(RAD51C):c.145+18C>A	LOC130061310, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O	GLikely benign
Select item 2708255	NM_058216.3(RAD51C):c.651A>C (p.Thr217=)	LOC129390903, RAD51C	Single nucleotide variant (synonymous variant +1 more)	Fanconi anemia complementation group O	GLikely benign
Select item 2705286	NM_058216.3(RAD51C):c.627T>G (p.Tyr209Ter)	LOC129390903, RAD51C (Y209*)	Single nucleotide variant (nonsense +1 more)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic
Select item 2698907	NM_058216.3(RAD51C):c.639T>C (p.Cys213=)	LOC129390903, RAD51C	Single nucleotide variant (synonymous variant +1 more)	Fanconi anemia complementation group O	GLikely benign
Select item 2695444	NM_058216.3(RAD51C):c.622A>T (p.Ile208Phe)	LOC129390903, RAD51C (I208F)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O	GUncertain significance
Select item 2695443	NM_058216.3(RAD51C):c.620A>T (p.His207Leu)	LOC129390903, RAD51C (H207L)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O	GUncertain significance
Select item 2678176	NM_058216.3(RAD51C):c.974delinsAA (p.Thr325fs)	RAD51C (T325fs)	Indel (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3	GLikely pathogenic
Select item 2678173	NM_058216.3(RAD51C):c.952del (p.Asp318fs)	RAD51C (D318fs)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3	GLikely pathogenic
Select item 2678172	NM_058216.3(RAD51C):c.905-7C>G	RAD51C	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 3	GUncertain significance
Select item 2678171	NM_058216.3(RAD51C):c.561dup (p.Lys188fs)	RAD51C (K188fs)	Duplication (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 3	GLikely pathogenic
Select item 2678169	NM_058216.3(RAD51C):c.475G>C (p.Asp159His)	RAD51C (D159H)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 3	GUncertain significance
Select item 2678168	NM_058216.3(RAD51C):c.682G>A (p.Asp228Asn)	LOC129390903, RAD51C (D228N)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3	GUncertain significance
Select item 2678167	NM_058216.3(RAD51C):c.422A>T (p.Asp141Val)	RAD51C (D141V)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 3	GUncertain significance
Select item 2625137	NM_058216.3(RAD51C):c.673C>T (p.Leu225Phe)	LOC129390903, RAD51C (L225F)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 2625135	NM_058216.1:c.371_372insALU	RAD51C	Insertion	Hereditary cancer-predisposing syndrome	GLikely pathogenic
Select item 2581147	GRCh37/hg19 17q22(chr17:56787220-56811584)x1	RAD51C	Copy number loss	Breast-ovarian cancer, familial, susceptibility to, 3 +1 more	Gnot provided
Select item 2580946	NM_058216.3:c.-20_705+5del	RAD51C	Deletion	Breast-ovarian cancer, familial, susceptibility to, 3	GLikely pathogenic
Select item 2573245	NM_058216.3(RAD51C):c.145+2T>C	LOC130061310, RAD51C	Single nucleotide variant (splice donor variant)	Breast-ovarian cancer, familial, susceptibility to, 3	GLikely pathogenic
Select item 2562777	NM_058216.3(RAD51C):c.619C>T (p.His207Tyr)	LOC129390903, RAD51C (H207Y)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +1 more	GUncertain significance
Select item 2562775	NM_058216.3(RAD51C):c.650C>G (p.Thr217Arg)	LOC129390903, RAD51C (T217R)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 2445289	NM_058216.3(RAD51C):c.107A>G (p.Glu36Gly)	RAD51C (E36G)	Single nucleotide variant (missense variant +1 more)	Ovarian cancer	GBenign
Select item 2165053	NM_058216.3(RAD51C):c.145+11C>T	LOC130061310, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O	GLikely benign
Select item 2162639	NM_058216.3(RAD51C):c.702A>G (p.Ser234=)	LOC129390903, RAD51C	Single nucleotide variant (synonymous variant +1 more)	Fanconi anemia complementation group O	GLikely benign
Select item 2091674	NM_058216.3(RAD51C):c.705+13C>A	LOC129390903, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O	GLikely benign
Select item 2063419	NM_058216.3(RAD51C):c.702A>C (p.Ser234=)	LOC129390903, RAD51C	Single nucleotide variant (synonymous variant +1 more)	Fanconi anemia complementation group O	GLikely benign
Select item 2032559	NM_058216.3(RAD51C):c.145+10C>A	LOC130061310, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O	GLikely benign
Select item 2021697	NM_058216.3(RAD51C):c.615_618del (p.Ser206fs)	LOC129390903, RAD51C (S206fs)	Microsatellite (frameshift variant +1 more)	Fanconi anemia complementation group O +1 more	GPathogenic/Likely pathogenic
Select item 2008568	NM_058216.3(RAD51C):c.658C>G (p.Leu220Val)	LOC129390903, RAD51C (L220V)	Single nucleotide variant (non-coding transcript variant +1 more)	Fanconi anemia complementation group O	GUncertain significance
Select item 1973089	NM_058216.3(RAD51C):c.705+16C>G	LOC129390903, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O	GLikely benign
Select item 1957377	NM_058216.3(RAD51C):c.617C>A (p.Ser206Tyr)	LOC129390903, RAD51C (S206Y)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +1 more	GUncertain significance
Select item 1809539	NM_058216.2:c.-71_837dup	RAD51C	Duplication	not provided	GUncertain significance
Select item 1756885	NM_058216.3(RAD51C):c.705+2_705+3insC	LOC129390903, RAD51C	Insertion (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1754646	NM_058216.3(RAD51C):c.664_681del (p.Gln222_Pro227del)	LOC129390903, RAD51C	Deletion (inframe_deletion +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1754562	NM_058216.3(RAD51C):c.662C>T (p.Ala221Val)	LOC129390903, RAD51C (A221V)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1754151	NM_058216.3(RAD51C):c.654G>C (p.Glu218Asp)	LOC129390903, RAD51C (E218D)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1753225	NM_058216.3(RAD51C):c.638G>A (p.Cys213Tyr)	LOC129390903, RAD51C (C213Y)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1751885	NM_058216.3(RAD51C):c.615_616del (p.His207fs)	LOC129390903, RAD51C (H207fs)	Deletion (frameshift variant +1 more)	Hereditary cancer-predisposing syndrome	GPathogenic
Select item 1751727	NM_058216.3(RAD51C):c.611T>A (p.Ile204Asn)	LOC129390903, RAD51C (I204N)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1719318	NM_058216.3(RAD51C):c.602T>G (p.Leu201Arg)	LOC129390903, RAD51C (L201R)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O	GUncertain significance
Select item 1717623	NM_058216.3(RAD51C):c.608A>G (p.Asn203Ser)	LOC129390903, RAD51C (N203S)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O	GUncertain significance
Select item 1692066	NM_058216.3(RAD51C):c.667G>T (p.Val223Phe)	LOC129390903, RAD51C (V223F)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1692065	NM_058216.3(RAD51C):c.624T>G (p.Ile208Met)	LOC129390903, RAD51C (I208M)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1656300	NM_058216.3(RAD51C):c.669T>C (p.Val223=)	LOC129390903, RAD51C	Single nucleotide variant (synonymous variant +1 more)	Fanconi anemia complementation group O	GLikely benign
Select item 1626173	NM_058216.3(RAD51C):c.615T>C (p.Leu205=)	LOC129390903, RAD51C	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1621291	NM_058216.3(RAD51C):c.690T>C (p.Leu230=)	LOC129390903, RAD51C	Single nucleotide variant (synonymous variant +1 more)	Fanconi anemia complementation group O	GLikely benign
Select item 1612747	NM_058216.3(RAD51C):c.145+16G>A	LOC130061310, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O	GLikely benign
Select item 1587677	NM_058216.3(RAD51C):c.651A>G (p.Thr217=)	LOC129390903, RAD51C	Single nucleotide variant (synonymous variant +1 more)	Fanconi anemia complementation group O +1 more	GLikely benign
Select item 1575493	NM_058216.3(RAD51C):c.657A>G (p.Leu219=)	LOC129390903, RAD51C	Single nucleotide variant (synonymous variant +1 more)	Fanconi anemia complementation group O	GLikely benign
Select item 1574966	NM_058216.3(RAD51C):c.145+13G>C	LOC130061310, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O	GLikely benign
Select item 1533908	NM_058216.3(RAD51C):c.145+7_145+17del	LOC130061310, RAD51C	Deletion (intron variant)	Fanconi anemia complementation group O	GLikely benign
Select item 1522818	NM_058216.3(RAD51C):c.638G>C (p.Cys213Ser)	LOC129390903, RAD51C (C213S)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O	GUncertain significance
Select item 1439892	NM_058216.3(RAD51C):c.692del (p.Leu230_Ser231insTer)	LOC129390903, RAD51C	Deletion (nonsense +1 more)	Fanconi anemia complementation group O	GPathogenic
Select item 1402456	NM_058216.3(RAD51C):c.645C>G (p.Asp215Glu)	LOC129390903, RAD51C (D215E)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O	GUncertain significance
Select item 1401730	NM_058216.3(RAD51C):c.688del (p.Leu230fs)	LOC129390903, RAD51C (L230fs)	Deletion (frameshift variant +1 more)	Fanconi anemia complementation group O	GPathogenic
Select item 1393407	NM_058216.3(RAD51C):c.145+18C>T	LOC130061310, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O	GUncertain significance
Select item 1379240	NM_058216.3(RAD51C):c.626A>T (p.Tyr209Phe)	LOC129390903, RAD51C (Y209F)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O	GUncertain significance

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