C3150659[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 484753	NM_058216.3(RAD51C):c.14C>G (p.Thr5Arg)	RAD51C (T5R)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 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 1797407	NM_058216.3(RAD51C):c.28A>G (p.Met10Val)	RAD51C (M10V)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +2 more	GUncertain significance
Select item 482159	NM_058216.3(RAD51C):c.28A>T (p.Met10Leu)	RAD51C (M10L)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +4 more	GUncertain significance
Select item 1062191	NM_058216.3(RAD51C):c.29T>C (p.Met10Thr)	RAD51C (M10T)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +1 more	GUncertain significance
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 649253	NM_058216.3(RAD51C):c.34C>G (p.Arg12Gly)	RAD51C (R12G)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +2 more	GUncertain significance
Select item 409837	NM_058216.3(RAD51C):c.34C>T (p.Arg12Trp)	RAD51C (R12W)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 653763	NM_058216.3(RAD51C):c.52_53del (p.Pro18fs)	RAD51C (P18fs)	Deletion (frameshift variant +1 more)	Fanconi anemia complementation group O +2 more	GPathogenic/Likely pathogenic
Select item 232581	NM_058216.3(RAD51C):c.52C>T (p.Pro18Ser)	RAD51C (P18S)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 835311	NM_058216.3(RAD51C):c.68_72dup (p.Val25fs)	RAD51C (V25fs)	Duplication (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +1 more	GPathogenic
Select item 229691	NM_058216.3(RAD51C):c.71G>A (p.Arg24Gln)	RAD51C (R24Q)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 480515	NM_058216.3(RAD51C):c.73G>A (p.Val25Met)	RAD51C (V25M)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 140837	NM_058216.3(RAD51C):c.80T>C (p.Leu27Pro)	RAD51C (L27P)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +3 more	GUncertain significance
Select item 482167	NM_058216.3(RAD51C):c.82G>C (p.Val28Leu)	RAD51C (V28L)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 232301	NM_058216.3(RAD51C):c.86C>T (p.Ser29Phe)	RAD51C (S29F)	Single nucleotide variant (missense variant +1 more)	not specified +4 more	GUncertain significance
Select item 480944	NM_058216.3(RAD51C):c.89C>T (p.Ala30Val)	RAD51C (A30V)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 182847	NM_058216.3(RAD51C):c.93del (p.Phe32fs)	RAD51C (F32fs)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +5 more	GPathogenic
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 933256	NM_058216.3(RAD51C):c.101C>T (p.Thr34Ile)	RAD51C (T34I)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +1 more	GUncertain significance
Select item 216803	NM_058216.3(RAD51C):c.106G>A (p.Glu36Lys)	RAD51C (E36K)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +4 more	GConflicting classifications of pathogenicity
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 1770324	NM_058216.3(RAD51C):c.133G>A (p.Glu45Lys)	RAD51C (E45K)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 484741	NM_058216.3(RAD51C):c.145+1G>A	RAD51C	Single nucleotide variant (splice donor variant)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic/Likely pathogenic
Select item 233766	NM_058216.3(RAD51C):c.145+1G>T	RAD51C	Single nucleotide variant (splice donor variant)	not provided +3 more	GPathogenic/Likely pathogenic
Select item 939186	NM_058216.3(RAD51C):c.146-7C>G	RAD51C	Single nucleotide variant (intron variant)	not provided +3 more	GUncertain significance
Select item 482181	NM_058216.3(RAD51C):c.146-4_146-2del	RAD51C	Deletion (splice acceptor variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely pathogenic
Select item 182830	NM_058216.3(RAD51C):c.154A>C (p.Ile52Leu)	RAD51C (I52L)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
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 1455900	NM_058216.3(RAD51C):c.168del (p.Ala57fs)	RAD51C (A57fs)	Deletion (frameshift variant +1 more)	Fanconi anemia complementation group O +1 more	GPathogenic/Likely pathogenic
Select item 187716	NM_058216.3(RAD51C):c.181_182del (p.Leu61fs)	RAD51C (L61fs)	Microsatellite (frameshift variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GPathogenic
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 1196279	NM_058216.3(RAD51C):c.194G>C (p.Arg65Thr)	RAD51C (R65T)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 820489	NM_058216.3(RAD51C):c.199G>C (p.Glu67Gln)	RAD51C (E67Q)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +1 more	GUncertain significance
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 2765342	NM_058216.3(RAD51C):c.208A>T (p.Thr70Ser)	RAD51C (T70S)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +1 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 820777	NM_058216.3(RAD51C):c.212A>G (p.Asn71Ser)	RAD51C (N71S)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 820776	NM_058216.3(RAD51C):c.212A>C (p.Asn71Thr)	RAD51C (N71T)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1054277	NM_058216.3(RAD51C):c.217C>T (p.Pro73Ser)	RAD51C (P73S)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 820944	NM_058216.3(RAD51C):c.224_225dup (p.Ala76fs)	RAD51C (A76fs)	Microsatellite (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3 +4 more	GPathogenic/Likely pathogenic
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 538766	NM_058216.3(RAD51C):c.245A>G (p.His82Arg)	RAD51C (H82R)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 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 186362	NM_058216.3(RAD51C):c.252G>T (p.Lys84Asn)	RAD51C (K84N)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GUncertain significance
Select item 484730	NM_058216.3(RAD51C):c.254G>A (p.Cys85Tyr)	RAD51C (C85Y)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
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 1039378	NM_058216.3(RAD51C):c.269T>G (p.Leu90Arg)	RAD51C (L90R)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +2 more	GUncertain significance
Select item 241769	NM_058216.3(RAD51C):c.274G>A (p.Glu92Lys)	RAD51C (E92K)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 835607	NM_058216.3(RAD51C):c.280G>A (p.Glu94Lys)	RAD51C (E94K)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +2 more	GUncertain significance
Select item 821879	NM_058216.3(RAD51C):c.283C>T (p.His95Tyr)	RAD51C (H95Y)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +2 more	GUncertain significance
Select item 2110767	NM_058216.3(RAD51C):c.286A>G (p.Thr96Ala)	RAD51C (T96A)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +2 more	GUncertain significance
Select item 538765	NM_058216.3(RAD51C):c.293G>T (p.Gly98Val)	RAD51C (G98V)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 409839	NM_058216.3(RAD51C):c.293G>C (p.Gly98Ala)	RAD51C (G98A)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 661813	NM_058216.3(RAD51C):c.335G>A (p.Gly112Glu)	RAD51C (G112E)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 142093	NM_058216.3(RAD51C):c.335G>C (p.Gly112Ala)	RAD51C (G112A)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +5 more	GConflicting classifications of pathogenicity
Select item 654903	NM_058216.3(RAD51C):c.344T>C (p.Val115Ala)	RAD51C (V115A)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1969528	NM_058216.3(RAD51C):c.346C>T (p.Pro116Ser)	RAD51C (P116S)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +1 more	GUncertain significance
Select item 496503	NM_058216.3(RAD51C):c.370T>A (p.Cys124Ser)	RAD51C (C124S)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group O +5 more	GUncertain significance
Select item 409836	NM_058216.3(RAD51C):c.373G>A (p.Gly125Ser)	RAD51C (G125S)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 2708888	NM_058216.3(RAD51C):c.383G>T (p.Gly128Val)	RAD51C (G128V)	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 182834	NM_058216.3(RAD51C):c.395C>G (p.Thr132Arg)	RAD51C (T132R)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 2678174	NM_058216.3(RAD51C):c.399dup (p.Leu134fs)	RAD51C (L134fs)	Duplication (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 3	GPathogenic/Likely pathogenic
Select item 233936	NM_058216.3(RAD51C):c.397C>A (p.Gln133Lys)	RAD51C (Q133K)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 230813	NM_058216.3(RAD51C):c.397C>G (p.Gln133Glu)	RAD51C (Q133E)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 31556	NM_058216.3(RAD51C):c.397C>T (p.Gln133Ter)	RAD51C (Q133*)	Single nucleotide variant (nonsense +1 more)	Breast and/or ovarian cancer +5 more	GPathogenic
Select item 234175	NM_058216.3(RAD51C):c.404G>A (p.Cys135Tyr)	RAD51C (C135Y +1 more)	Single nucleotide variant (nonsense +2 more)	not provided +4 more	GPathogenic/Likely pathogenic
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 409834	NM_058216.3(RAD51C):c.405-1G>A	RAD51C	Single nucleotide variant (splice acceptor variant)	Fanconi anemia complementation group O +1 more	GLikely pathogenic
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 1438265	NM_058216.3(RAD51C):c.407T>G (p.Met136Arg)	RAD51C (M136R)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group O +2 more	GUncertain significance
Select item 925917	NM_058216.3(RAD51C):c.409C>T (p.Gln137Ter)	RAD51C (Q137*)	Single nucleotide variant (nonsense)	Fanconi anemia complementation group O +2 more	GPathogenic
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 628696	NM_058216.3(RAD51C):c.416C>T (p.Ala139Val)	RAD51C (A139V)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group O +2 more	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 128205	NM_058216.3(RAD51C):c.428A>G (p.Gln143Arg)	RAD51C (Q143R)	Single nucleotide variant (missense variant)	not provided +4 more	GUncertain significance
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 484757	NM_058216.3(RAD51C):c.440G>A (p.Cys147Tyr)	RAD51C (C147Y)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 824895	NM_058216.3(RAD51C):c.443T>G (p.Phe148Cys)	RAD51C (F148C)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 3 +1 more	GUncertain significance
Select item 645241	NM_058216.3(RAD51C):c.447_448delinsT (p.Gly150fs)	RAD51C (G150fs)	Indel (frameshift variant)	Breast-ovarian cancer, familial, susceptibility to, 3 +2 more	GPathogenic/Likely pathogenic
Select item 492369	NM_058216.3(RAD51C):c.448G>A (p.Gly150Arg)	RAD51C (G150R)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 3 +2 more	GUncertain significance
Select item 409833	NM_058216.3(RAD51C):c.451G>C (p.Val151Leu)	RAD51C (V151L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 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 185444	NM_058216.3(RAD51C):c.458G>A (p.Gly153Asp)	RAD51C (G153D)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
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 1069820	NM_058216.3(RAD51C):c.472dup (p.Ile158fs)	RAD51C (I158fs)	Duplication (frameshift variant)	Fanconi anemia complementation group O +1 more	GPathogenic/Likely 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 185073	NM_058216.3(RAD51C):c.477T>G (p.Asp159Glu)	RAD51C (D159E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 565947	NM_058216.3(RAD51C):c.483G>T (p.Glu161Asp)	RAD51C (E161D)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group O +2 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 1053502	NM_058216.3(RAD51C):c.500A>G (p.Asp167Gly)	RAD51C (D167G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 141095	NM_058216.3(RAD51C):c.502A>T (p.Arg168Ter)	RAD51C (R168*)	Single nucleotide variant (nonsense)	Fanconi anemia complementation group O +3 more	GPathogenic
Select item 825532	NM_058216.3(RAD51C):c.519dup (p.Thr174fs)	RAD51C (T174fs)	Duplication (frameshift variant)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic/Likely pathogenic
Select item 219853	NM_058216.3(RAD51C):c.520A>G (p.Thr174Ala)	RAD51C (T174A)	Single nucleotide variant (missense variant)	Breast-ovarian cancer, familial, susceptibility to, 3 +3 more	GUncertain significance
Select item 409827	NM_058216.3(RAD51C):c.525dup (p.Cys176fs)	RAD51C (C176fs)	Duplication (frameshift variant)	not provided +3 more	GPathogenic

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