ClinVar for Gene (Select 7414) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3226301	NM_014000.3(VCL):c.762T>G (p.Asp254Glu)	VCL (D254E)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3226300	NM_014000.3(VCL):c.592G>T (p.Val198Leu)	VCL (V198L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3226298	NM_014000.3(VCL):c.3390T>C (p.Thr1130=)	VCL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3226297	NM_014000.3(VCL):c.3138A>G (p.Arg1046=)	VCL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3226296	NM_014000.3(VCL):c.2825_2827delinsTCG (p.Pro942_Pro943delinsLeuAla)	VCL	Indel (missense variant +1 more)	Cardiovascular phenotype	GUncertain significance
Select item 3226295	NM_014000.3(VCL):c.2823C>G (p.Val941=)	VCL	Single nucleotide variant (synonymous variant +1 more)	Cardiovascular phenotype	GLikely benign
Select item 3226294	NM_014000.3(VCL):c.2697G>A (p.Met899Ile)	VCL (M899I)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3226293	NM_014000.3(VCL):c.2688G>A (p.Gln896=)	VCL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3226292	NM_014000.3(VCL):c.254G>A (p.Cys85Tyr)	VCL (C85Y)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3226291	NM_014000.3(VCL):c.1862A>G (p.Asn621Ser)	VCL (N621S)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GLikely benign
Select item 3226290	NM_014000.3(VCL):c.1782A>T (p.Glu594Asp)	VCL (E594D)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3226289	NM_014000.3(VCL):c.169-4G>C	VCL	Single nucleotide variant (intron variant)	Cardiovascular phenotype	GLikely benign
Select item 3226288	NM_014000.3(VCL):c.1631A>G (p.Lys544Arg)	VCL (K544R)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3226287	NM_014000.3(VCL):c.1605G>T (p.Gly535=)	VCL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3226286	NM_014000.3(VCL):c.1422G>T (p.Gln474His)	VCL (Q474H)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3226285	NM_014000.3(VCL):c.1422G>A (p.Gln474=)	VCL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3226284	NM_014000.3(VCL):c.1254A>G (p.Ile418Met)	VCL (I418M)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3226283	NM_014000.3(VCL):c.1244C>A (p.Ala415Asp)	VCL (A415D)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3226282	NM_014000.3(VCL):c.1217A>G (p.Glu406Gly)	VCL (E406G)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3188356	NM_014000.3(VCL):c.2189T>C (p.Ile730Thr)	VCL (I730T)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3069078	NM_014000.3(VCL):c.8T>C (p.Val3Ala)	VCL, LOC130004109 (V3A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3065902	NM_014000.3(VCL):c.2359T>A (p.Ser787Thr)	VCL (S787T)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 15	GUncertain significance
Select item 3065159	NM_014000.3(VCL):c.2512C>T (p.Gln838Ter)	VCL (Q838*)	Single nucleotide variant (nonsense)	Hypertrophic cardiomyopathy 15	GUncertain significance
Select item 3022134	NM_014000.3(VCL):c.180G>A (p.Glu60=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 3021364	NM_014000.3(VCL):c.2434+16C>A	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 3020929	NM_014000.3(VCL):c.1660C>G (p.Gln554Glu)	VCL (Q554E)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 3018293	NM_014000.3(VCL):c.1744-19T>C	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 3016820	NM_014000.3(VCL):c.500-11T>G	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 3016182	NM_014000.3(VCL):c.747A>G (p.Gln249=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 3016066	NM_014000.3(VCL):c.3153+7G>A	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 3011039	NM_014000.3(VCL):c.1176+11T>G	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 3008952	NM_014000.3(VCL):c.2538A>G (p.Pro846=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 3006858	NM_014000.3(VCL):c.1047C>T (p.Ala349=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2998537	NM_014000.3(VCL):c.1793T>C (p.Val598Ala)	VCL (V598A)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2998432	NM_014000.3(VCL):c.3233_3235del (p.Asn1078del)	VCL (N1010del +1 more)	Deletion (inframe_deletion)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2997888	NM_014000.3(VCL):c.1371A>G (p.Pro457=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2996573	NM_014000.3(VCL):c.980T>C (p.Met327Thr)	VCL (M327T)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2994546	NM_014000.3(VCL):c.183T>G (p.Thr61=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2993853	NM_014000.3(VCL):c.704A>G (p.Glu235Gly)	VCL (E235G)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2993782	NM_014000.3(VCL):c.1687G>A (p.Glu563Lys)	VCL (E563K)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2989468	NM_014000.3(VCL):c.1728C>T (p.Leu576=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2987851	NM_014000.3(VCL):c.2721T>C (p.Asp907=)	VCL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 2987142	NM_014000.3(VCL):c.1873-15T>C	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2985960	NM_014000.3(VCL):c.2746-13G>C	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2983585	NM_014000.3(VCL):c.2277G>T (p.Arg759=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2982127	NM_014000.3(VCL):c.2693T>C (p.Met898Thr)	VCL (M898T)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2980081	NM_014000.3(VCL):c.784-16dup	VCL	Duplication (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2978472	NM_014000.3(VCL):c.2028C>T (p.Val676=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2970482	NM_014000.3(VCL):c.1120C>T (p.Leu374=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2961243	NM_014000.3(VCL):c.1291A>G (p.Ile431Val)	VCL (I431V)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2958010	NM_014000.3(VCL):c.2828C>A (p.Pro943His)	VCL (P943H)	Single nucleotide variant (missense variant +1 more)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2955271	NM_014000.3(VCL):c.1438G>A (p.Ala480Thr)	VCL (A480T)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2920477	NM_014000.3(VCL):c.2746-13G>A	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2918261	NM_014000.3(VCL):c.1743+4G>A	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2916295	NM_014000.3(VCL):c.578A>G (p.Asn193Ser)	VCL (N193S)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2916255	NM_014000.3(VCL):c.1743+12G>T	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2914952	NM_014000.3(VCL):c.77T>G (p.Met26Arg)	LOC130004109, VCL (M26R)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2914604	NM_014000.3(VCL):c.168+18G>T	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2913562	NM_014000.3(VCL):c.2920C>T (p.His974Tyr)	VCL (H974Y)	Single nucleotide variant (missense variant +1 more)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2913496	NM_014000.3(VCL):c.461T>C (p.Met154Thr)	VCL (M154T)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2912369	NM_014000.3(VCL):c.3306G>A (p.Val1102=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2911917	NM_014000.3(VCL):c.2949+17C>T	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2911820	NM_014000.3(VCL):c.630G>T (p.Lys210Asn)	VCL (K210N)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2910517	NM_014000.3(VCL):c.2746-15C>G	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2909044	NM_014000.3(VCL):c.1861A>G (p.Asn621Asp)	VCL (N621D)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2905149	NM_014000.3(VCL):c.3153+46_3153+47insCGTGCGTGTGTGTGTGTGTGTGTGTGTGTG	VCL	Insertion (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2905031	NM_014000.3(VCL):c.1544-20T>C	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2904661	NM_014000.3(VCL):c.271G>T (p.Ala91Ser)	VCL (A91S)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2903848	NM_014000.3(VCL):c.2950-20_2950-19del	VCL	Deletion (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2903448	NM_014000.3(VCL):c.2225C>A (p.Ala742Asp)	VCL (A742D)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2898765	NM_014000.3(VCL):c.3357T>C (p.Asp1119=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2898009	NM_014000.3(VCL):c.1177-7T>C	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2897327	NM_014000.3(VCL):c.3153+14G>T	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2894584	NM_014000.3(VCL):c.1055A>C (p.Lys352Thr)	VCL (K352T)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2890720	NM_014000.3(VCL):c.1908T>C (p.His636=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2887476	NM_014000.3(VCL):c.2023-13T>C	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2885990	NM_014000.3(VCL):c.875-6T>C	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2885761	NM_014000.3(VCL):c.711G>A (p.Met237Ile)	VCL (M237I)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2884302	NM_014000.3(VCL):c.390+12G>C	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2875884	NM_014000.3(VCL):c.2439G>A (p.Leu813=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2871573	NM_014000.3(VCL):c.2835G>T (p.Met945Ile)	VCL (M945I)	Single nucleotide variant (missense variant +1 more)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2868857	NM_014000.3(VCL):c.2132-19A>G	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2866381	NM_014000.3(VCL):c.318T>C (p.Asp106=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2865162	NM_014000.3(VCL):c.336A>C (p.Ser112=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2861971	NM_014000.3(VCL):c.2132-6T>C	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2861962	NM_014000.3(VCL):c.237T>A (p.Ile79=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2861182	NM_014000.3(VCL):c.273A>T (p.Ala91=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2861181	NM_014000.3(VCL):c.269A>T (p.Gln90Leu)	VCL (Q90L)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2858270	NM_014000.3(VCL):c.536A>G (p.Gln179Arg)	VCL (Q179R)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2857546	NM_014000.3(VCL):c.2000C>A (p.Thr667Lys)	VCL (T667K)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2854895	NM_014000.3(VCL):c.2272C>G (p.Arg758Gly)	VCL (R758G)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2853427	NM_014000.3(VCL):c.3153+21_3153+28del	VCL	Deletion (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2850869	NM_014000.3(VCL):c.2089_2103del (p.Thr697_Gln701del)	VCL	Deletion (inframe_deletion)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2848125	NM_014000.3(VCL):c.702A>T (p.Val234=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2847679	NM_014000.3(VCL):c.2748G>C (p.Pro916=)	VCL	Single nucleotide variant (synonymous variant +1 more)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2847400	NM_014000.3(VCL):c.1248G>C (p.Arg416=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2845326	NM_014000.3(VCL):c.1746T>C (p.Asp582=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2843272	NM_014000.3(VCL):c.870C>T (p.Ser290=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2841046	NM_014000.3(VCL):c.1420C>A (p.Gln474Lys)	VCL (Q474K)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2839467	NM_014000.3(VCL):c.2022+5G>A	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GUncertain significance

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