VCL[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 148945	GRCh38/hg38 10q11.23-23.2(chr10:50729367-87147204)x3	LOC126860963, LOC126860964 +1008 more	Copy number gain	See cases	GPathogenic
Select item 58726	GRCh38/hg38 10q21.1-22.2(chr10:58436466-74415216)x1	LOC129390190, LOC129390191 +610 more	Copy number loss	See cases	GPathogenic
Select item 147477	GRCh38/hg38 10q21.3-22.2(chr10:63402579-75296099)x1	ADAMTS14, ADK +514 more	Copy number loss	See cases	GPathogenic
Select item 146115	GRCh38/hg38 10q21.3-22.3(chr10:67196567-79422057)x3	ADAMTS14, ADK +580 more	Copy number gain	See cases	GPathogenic
Select item 58745	GRCh38/hg38 10q22.1-22.2(chr10:72720628-75612374)x1	LOC130004132, LOC130004133 +150 more	Copy number loss	See cases	GPathogenic
Select item 684057	NM_014000.2(VCL):c.-386A>G	LOC130004108, VCL	Single nucleotide variant	not provided	GBenign
Select item 684060	NM_014000.2(VCL):c.-264A>G	LOC130004108, VCL	Single nucleotide variant	not provided	GBenign
Select item 1205590	NC_000010.11:g.73998025C>T	LOC130004108, VCL	Single nucleotide variant	not provided	GLikely benign
Select item 1188273	NC_000010.11:g.73998048G>A	LOC130004108, VCL	Single nucleotide variant	not provided	GLikely benign
Select item 879267	NM_014000.2(VCL):c.-96C>T	VCL	Single nucleotide variant	Dilated cardiomyopathy 1W	GUncertain significance
Select item 300780	NM_014000.3(VCL):c.-62T>G	LOC130004109, VCL	Single nucleotide variant (5 prime UTR variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 879268	NM_014000.3(VCL):c.-58G>T	LOC130004109, VCL	Single nucleotide variant (5 prime UTR variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 651810	NC_000010.11:g.(?_73998188)_(73998395_?)del	LOC130004109, VCL	Deletion	Dilated cardiomyopathy 1W	GUncertain significance
Select item 381051	NM_014000.3(VCL):c.-13G>A	LOC130004109, VCL	Single nucleotide variant (5 prime UTR variant)	not specified	GLikely benign
Select item 2565624	NM_014000.3(VCL):c.-4C>T	LOC130004109, VCL	Single nucleotide variant (5 prime UTR variant)	Cardiovascular phenotype	GUncertain significance
Select item 2056170	NM_014000.3(VCL):c.4C>G (p.Pro2Ala)	LOC130004109, VCL (P2A)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W +1 more	GUncertain significance
Select item 1628677	NM_014000.3(VCL):c.6A>C (p.Pro2=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 1053516	NM_014000.3(VCL):c.14A>C (p.His5Pro)	LOC130004109, VCL (H5P)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 1142391	NM_014000.3(VCL):c.18G>A (p.Thr6=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 1378723	NM_014000.3(VCL):c.20G>A (p.Arg7His)	LOC130004109, VCL (R7H)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W +1 more	GUncertain significance
Select item 640967	NM_014000.3(VCL):c.20G>T (p.Arg7Leu)	LOC130004109, VCL (R7L)	Single nucleotide variant (missense variant)	Inborn genetic diseases +3 more	GUncertain significance
Select item 2420063	NM_014000.3(VCL):c.24G>A (p.Thr8=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 701969	NM_014000.3(VCL):c.24G>T (p.Thr8=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1584677	NM_014000.3(VCL):c.27C>T (p.Ile9=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 796440	NM_014000.3(VCL):c.30G>A (p.Glu10=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 45607	NM_014000.3(VCL):c.31A>G (p.Ser11Gly)	LOC130004109, VCL (S11G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 536703	NM_014000.3(VCL):c.32G>A (p.Ser11Asn)	LOC130004109, VCL (S11N)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 879269	NM_014000.3(VCL):c.36C>T (p.Ile12=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W +1 more	GConflicting classifications of pathogenicity
Select item 240882	NM_014000.3(VCL):c.45G>A (p.Pro15=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Dilated Cardiomyopathy, Dominant +2 more	GConflicting classifications of pathogenicity
Select item 202152	NM_014000.3(VCL):c.50C>A (p.Ala17Glu)	LOC130004109, VCL (A17E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1112564	NM_014000.3(VCL):c.51A>G (p.Ala17=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1012146	NM_014000.3(VCL):c.53A>G (p.Gln18Arg)	LOC130004109, VCL (Q18R)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 1753297	NM_014000.3(VCL):c.63C>G (p.Ser21=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 1756573	NM_014000.3(VCL):c.69G>A (p.Leu23=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 761580	NM_014000.3(VCL):c.69G>C (p.Leu23=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 1759712	NM_014000.3(VCL):c.75A>C (p.Ile25=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
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 1723062	NM_014000.3(VCL):c.79C>G (p.His27Asp)	LOC130004109, VCL (H27D)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W +2 more	GUncertain significance
Select item 202145	NM_014000.3(VCL):c.81C>T (p.His27=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +3 more	GConflicting classifications of pathogenicity
Select item 1658519	NM_014000.3(VCL):c.87G>A (p.Glu29=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 963301	NM_014000.3(VCL):c.98A>G (p.Asp33Gly)	LOC130004109, VCL (D33G)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 1105627	NM_014000.3(VCL):c.99C>T (p.Asp33=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1499651	NM_014000.3(VCL):c.103A>G (p.Lys35Glu)	LOC130004109, VCL (K35E)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 1505280	NM_014000.3(VCL):c.107C>T (p.Ala36Val)	LOC130004109, VCL (A36V)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 1797465	NM_014000.3(VCL):c.111T>C (p.Ile37=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 408943	NM_014000.3(VCL):c.113C>T (p.Pro38Leu)	LOC130004109, VCL (P38L)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 1723116	NM_014000.3(VCL):c.118C>G (p.Leu40Val)	LOC130004109, VCL (L40V)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W +2 more	GUncertain significance
Select item 1704564	NM_014000.3(VCL):c.120C>A (p.Leu40=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 166535	NM_014000.3(VCL):c.120C>T (p.Leu40=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +4 more	GBenign/Likely benign
Select item 1755187	NM_014000.3(VCL):c.122C>T (p.Thr41Ile)	LOC130004109, VCL (T41I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2099280	NM_014000.3(VCL):c.124G>A (p.Ala42Thr)	LOC130004109, VCL (A42T)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 793137	NM_014000.3(VCL):c.126G>T (p.Ala42=)	VCL, LOC130004109	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 1127343	NM_014000.3(VCL):c.129C>T (p.Pro43=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1802223	NM_014000.3(VCL):c.133G>C (p.Ala45Pro)	LOC130004109, VCL (A45P)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 1770329	NM_014000.3(VCL):c.133G>A (p.Ala45Thr)	LOC130004109, VCL (A45T)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W +1 more	GUncertain significance
Select item 1329297	NM_014000.3(VCL):c.134_135inv (p.Ala45Gly)	LOC130004109, VCL (A45G)	Inversion (missense variant)	Cardiomyopathy	GUncertain significance
Select item 2777013	NM_014000.3(VCL):c.135C>T (p.Ala45=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 1329298	NM_014000.3(VCL):c.135C>G (p.Ala45=)	LOC130004109, VCL	Single nucleotide variant (synonymous variant)	Cardiomyopathy	GLikely benign
Select item 2782911	NM_014000.3(VCL):c.136G>A (p.Ala46Thr)	LOC130004109, VCL (A46T)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 1771019	NM_014000.3(VCL):c.136G>T (p.Ala46Ser)	LOC130004109, VCL (A46S)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1329299	NM_014000.3(VCL):c.140T>G (p.Val47Gly)	VCL (V47G)	Single nucleotide variant (missense variant)	Cardiomyopathy	GUncertain significance
Select item 2478217	NM_014000.3(VCL):c.142C>G (p.Gln48Glu)	VCL (Q48E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1772464	NM_014000.3(VCL):c.142C>T (p.Gln48Ter)	VCL (Q48*)	Single nucleotide variant (nonsense)	Cardiovascular phenotype	GUncertain significance
Select item 1773127	NM_014000.3(VCL):c.145G>A (p.Ala49Thr)	VCL (A49T)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1773323	NM_014000.3(VCL):c.146C>G (p.Ala49Gly)	VCL (A49G)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 633014	NM_014000.3(VCL):c.151G>T (p.Val51Phe)	VCL (V51F)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2478109	NM_014000.3(VCL):c.155G>A (p.Ser52Asn)	VCL (S52N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 300781	NM_014000.3(VCL):c.155G>C (p.Ser52Thr)	VCL (S52T)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 1078138	NM_014000.3(VCL):c.156C>T (p.Ser52=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 417950	NM_014000.3(VCL):c.158A>G (p.Asn53Ser)	VCL (N53S)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 2716180	NM_014000.3(VCL):c.160C>T (p.Leu54Phe)	VCL (L54F)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 1009316	NM_014000.3(VCL):c.163G>C (p.Val55Leu)	VCL (V55L)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 229631	NM_014000.3(VCL):c.163G>T (p.Val55Phe)	VCL (V55F)	Single nucleotide variant (missense variant)	Cardiomyopathy +3 more	GUncertain significance
Select item 754213	NM_014000.3(VCL):c.165C>A (p.Val55=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 468810	NM_014000.3(VCL):c.166C>T (p.Arg56Trp)	VCL (R56W)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2193201	NM_014000.3(VCL):c.167G>A (p.Arg56Gln)	VCL (R56Q)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 2052227	NM_014000.3(VCL):c.168+1del	VCL	Deletion (splice donor variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1151932	NM_014000.3(VCL):c.168+7G>T	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 505151	NM_014000.3(VCL):c.168+9G>T	VCL	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 2914604	NM_014000.3(VCL):c.168+18G>T	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 1497024	NM_014000.3(VCL):c.168+28_168+39del	VCL	Deletion (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2728393	NM_014000.3(VCL):c.168+20C>T	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 383287	NM_014000.3(VCL):c.168+20C>A	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W +1 more	GLikely benign
Select item 671495	NM_014000.3(VCL):c.169-290A>G	VCL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1576162	NM_014000.3(VCL):c.169-20G>C	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2771715	NM_014000.3(VCL):c.169-19A>G	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 1616983	NM_014000.3(VCL):c.169-11dup	VCL	Duplication (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 506391	NM_014000.3(VCL):c.169-11del	VCL	Deletion (intron variant)	not specified +2 more	GBenign/Likely benign
Select item 384031	NM_014000.3(VCL):c.169-18T>A	VCL	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 536723	NM_014000.3(VCL):c.169-10C>G	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 510503	NM_014000.3(VCL):c.169-10delinsTG	VCL	Indel (intron variant)	Cardiomyopathy +1 more	GConflicting classifications of pathogenicity
Select item 1128904	NM_014000.3(VCL):c.169-9C>T	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 1587107	NM_014000.3(VCL):c.169-7C>T	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 415312	NM_014000.3(VCL):c.169-7C>G	VCL	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1W +1 more	GLikely benign
Select item 2586045	NM_014000.3(VCL):c.173G>C (p.Gly58Ala)	VCL (G58A)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1713383	NM_014000.3(VCL):c.173G>A (p.Gly58Glu)	VCL (G58E)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1W	GUncertain significance
Select item 1184903	NM_014000.3(VCL):c.176_177del (p.Lys59fs)	VCL (K59fs)	Deletion (frameshift variant)	not provided	GPathogenic
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 2994546	NM_014000.3(VCL):c.183T>G (p.Thr61=)	VCL	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1W	GLikely benign
Select item 2496583	NM_014000.3(VCL):c.184G>T (p.Val62Phe)	VCL (V62F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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