Il18 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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271 records found for search term Il18

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15151892	CV779427	single nucleotide variant	NM_001562.4(IL18):c.80-5C>A	not provided [RCV000968237]	benign	11	112153608	112153608	Human		name
21403990	CV800891	single nucleotide variant	NM_001562.4(IL18):c.-8-919T>C	Three Vessel Coronary Disease [RCV001003439]	benign	11	112155980	112155980	Human	1	name
21403989	CV800889	single nucleotide variant	NM_001562.4(IL18):c.361-1974C>T	Three Vessel Coronary Disease [RCV001003438]	benign	11	112145791	112145791	Human	1	name
15166613	CV752428	single nucleotide variant	NM_001562.4(IL18):c.216T>G (p.Ser72=)	not provided [RCV000926909]	likely benign	11	112150082	112150082	Human		name
21403988	CV800890	single nucleotide variant	NM_001562.4(IL18):c.105A>C (p.Ser35=)	Three Vessel Coronary Disease [RCV001003437]\|not provided [RCV004709018]	benign	11	112150193	112150193	Human	1	name
405804558	CV3271005	single nucleotide variant	NM_001562.4(IL18):c.74T>G (p.Phe25Cys)	not specified [RCV004405066]	uncertain significance	11	112154980	112154980	Human		name
407515715	CV3444526	single nucleotide variant	NM_001562.4(IL18):c.197T>G (p.Phe66Cys)	not specified [RCV004627977]	uncertain significance	11	112150101	112150101	Human		name
401757517	CV2707827	single nucleotide variant	NM_001562.4(IL18):c.500G>A (p.Arg167Lys)	not specified [RCV004309110]	uncertain significance	11	112143678	112143678	Human		name
405804556	CV3271004	single nucleotide variant	NM_001562.4(IL18):c.398G>A (p.Ser133Asn)	not specified [RCV004405065]	likely benign	11	112143780	112143780	Human		name
597793096	CV3690249	single nucleotide variant	NM_001562.4(IL18):c.446T>C (p.Met149Thr)	not specified [RCV004934091]	uncertain significance	11	112143732	112143732	Human		name
8633847	CV89063	single nucleotide variant	NM_001562.3(IL18):c.532G>A (p.Asp178Asn)	Malignant melanoma [RCV000069160]	not provided	11	112143646	112143646	Human		name
150339101	CV1108819	single nucleotide variant	NM_003855.5(IL18R1):c.810-56C>A	Ascending aortic dissection [RCV001543143]	association	2	102386805	102386805	Human	3	name
150339101	CV1108819	single nucleotide variant	NM_003855.5(IL18R1):c.810-56C>A	Ascending aortic dissection [RCV001543143]	association	2	102386805	102386806	Human	3	name
156020073	CV2046986	single nucleotide variant	NM_001039660.2(IL18BP):c.29-4T>A	not provided [RCV002780605]	likely benign\|uncertain significance	11	72000347	72000347	Human		name
405175515	CV2955541	duplication	NM_001039660.2(IL18BP):c.28+2dup	not provided [RCV003675703]	uncertain significance	11	72000013	72000014	Human		name
405244790	CV2968320	single nucleotide variant	NM_001039660.2(IL18BP):c.28+9T>A	not provided [RCV003684898]	uncertain significance	11	72000021	72000021	Human		name
405233421	CV2975356	single nucleotide variant	NM_001039660.2(IL18BP):c.29-3C>G	not provided [RCV003682632]	uncertain significance	11	72000348	72000348	Human		name
405094220	CV3045679	single nucleotide variant	NM_001039660.2(IL18BP):c.28+6C>T	not provided [RCV003718040]	uncertain significance	11	72000018	72000018	Human		name
597961340	CV3812122	single nucleotide variant	NM_001039660.2(IL18BP):c.28+1G>C	not provided [RCV005163775]	uncertain significance	11	72000013	72000013	Human		name
597922083	CV3861869	single nucleotide variant	NM_001039660.2(IL18BP):c.28+1G>T	not provided [RCV005205245]	uncertain significance	11	72000013	72000013	Human		name
38466204	CV904880	single nucleotide variant	NM_003855.5(IL18R1):c.59-1038C>A	Behcet disease [RCV001250485]	association	2	102366787	102366787	Human	1	name
150339098	CV1108818	single nucleotide variant	NM_003855.5(IL18R1):c.302+1284C>T	Ascending aortic dissection [RCV001543140]	association	2	102369352	102369352	Human	2	name
156262566	CV1913671	single nucleotide variant	NM_001039660.2(IL18BP):c.236-4C>T	not provided [RCV002627817]	uncertain significance	11	72001197	72001197	Human		name
155955907	CV2033406	single nucleotide variant	NM_001039660.2(IL18BP):c.29-19G>C	not provided [RCV002730926]	uncertain significance	11	72000332	72000332	Human		name
156159776	CV2033772	single nucleotide variant	NM_001039660.2(IL18BP):c.508-2A>T	not provided [RCV002741503]	uncertain significance	11	72001782	72001782	Human		name
156192455	CV2082965	single nucleotide variant	NM_001039660.2(IL18BP):c.29-19G>A	not provided [RCV002852183]	uncertain significance	11	72000332	72000332	Human		name
156356457	CV2126093	single nucleotide variant	NM_001039660.2(IL18BP):c.359+9C>T	not provided [RCV002966697]	benign	11	72001333	72001333	Human		name
156299396	CV2153490	single nucleotide variant	NM_001039660.2(IL18BP):c.28+13G>A	not provided [RCV003028018]	uncertain significance	11	72000025	72000025	Human		name
156326445	CV2160003	single nucleotide variant	NM_001039660.2(IL18BP):c.360-6C>T	not provided [RCV003029515]	uncertain significance	11	72001399	72001399	Human		name
156172739	CV2166117	single nucleotide variant	NM_001039660.2(IL18BP):c.507+6G>A	not provided [RCV003023565]	uncertain significance	11	72001558	72001558	Human		name
156307131	CV2167682	single nucleotide variant	NM_001039660.2(IL18BP):c.508-9C>T	not provided [RCV003045836]	uncertain significance	11	72001775	72001775	Human		name
156115481	CV2182891	single nucleotide variant	NM_001039660.2(IL18BP):c.360-8C>G	not provided [RCV003039108]	uncertain significance	11	72001397	72001397	Human		name
405052897	CV2893749	single nucleotide variant	NM_001039660.2(IL18BP):c.28+16A>G	not provided [RCV003579918]	uncertain significance	11	72000028	72000028	Human		name
402471367	CV2908098	single nucleotide variant	NM_001039660.2(IL18BP):c.236-6C>T	not provided [RCV003570421]	likely benign	11	72001195	72001195	Human		name
405149220	CV2960213	single nucleotide variant	NM_001039660.2(IL18BP):c.508-1G>A	not provided [RCV003669882]	uncertain significance	11	72001783	72001783	Human		name
405189714	CV2968486	single nucleotide variant	NM_001039660.2(IL18BP):c.29-18T>C	not provided [RCV003677092]	uncertain significance	11	72000333	72000333	Human		name
405083773	CV3017246	single nucleotide variant	NM_001039660.2(IL18BP):c.508-4C>T	not provided [RCV003699234]	benign	11	72001780	72001780	Human		name
405144134	CV3027270	single nucleotide variant	NM_001039660.2(IL18BP):c.28+18G>A	not provided [RCV003702772]	likely benign\|uncertain significance	11	72000030	72000030	Human		name
405178538	CV3027573	single nucleotide variant	NM_001039660.2(IL18BP):c.507+1G>A	not provided [RCV003705311]	uncertain significance	11	72001553	72001553	Human		name
405066874	CV3030735	single nucleotide variant	NM_001039660.2(IL18BP):c.508-3T>C	not provided [RCV003697994]	uncertain significance	11	72001781	72001781	Human		name
597957860	CV3814481	single nucleotide variant	NM_001039660.2(IL18BP):c.360-2A>G	not provided [RCV005162812]	uncertain significance	11	72001403	72001403	Human		name
597876177	CV3829793	single nucleotide variant	NM_001039660.2(IL18BP):c.360-7G>A	not provided [RCV005177501]	likely benign	11	72001398	72001398	Human		name
597832075	CV3830900	single nucleotide variant	NM_001039660.2(IL18BP):c.28+13G>T	not provided [RCV005170298]	likely benign	11	72000025	72000025	Human		name
38466199	CV904878	single nucleotide variant	NM_003855.5(IL18R1):c.-29+1269C>T	Behcet disease [RCV001250484]\|not provided [RCV001683745]	association\|benign	2	102357669	102357669	Human	2	name
38466199	CV904878	single nucleotide variant	NM_003855.5(IL18R1):c.-29+1269C>T	Behcet disease [RCV001250484]\|not provided [RCV001683745]	association\|benign	2	102357669	102357670	Human	2	name
38466194	CV904879	single nucleotide variant	NM_003855.5(IL18R1):c.-29+2476T>G	Behcet disease [RCV001250483]	association	2	102358876	102358876	Human	4	name
156246692	CV2029426	single nucleotide variant	NM_001039660.2(IL18BP):c.235+11C>T	not provided [RCV002745851]	likely benign\|uncertain significance	11	72000568	72000568	Human		name
156136874	CV2032758	single nucleotide variant	NM_001039660.2(IL18BP):c.235+17T>G	not provided [RCV002740761]	likely benign	11	72000574	72000574	Human		name
156033406	CV2078997	single nucleotide variant	NM_001039660.2(IL18BP):c.508-14C>T	not provided [RCV002867147]	uncertain significance	11	72001770	72001770	Human		name
156167285	CV2102290	single nucleotide variant	NM_001039660.2(IL18BP):c.360-18C>G	not provided [RCV002891214]	uncertain significance	11	72001387	72001387	Human		name
156002636	CV2106859	single nucleotide variant	NM_001039660.2(IL18BP):c.359+10G>A	not provided [RCV002947864]	likely benign\|uncertain significance	11	72001334	72001334	Human		name
155941926	CV2229366	single nucleotide variant	NM_001039660.2(IL18BP):c.507+50A>T	not specified [RCV004101150]	uncertain significance	11	72001602	72001602	Human		name
401870591	CV2769300	single nucleotide variant	NM_001039660.2(IL18BP):c.507+80A>C	not specified [RCV004357302]	uncertain significance	11	72001632	72001632	Human		name
401933305	CV2813496	single nucleotide variant	NM_001039660.2(IL18BP):c.507+82A>T	not provided [RCV003409338]	likely benign	11	72001634	72001634	Human		name
404988142	CV2849465	single nucleotide variant	NM_001039660.2(IL18BP):c.236-72G>A	not specified [RCV003490322]	benign	11	72001129	72001129	Human		name
405086550	CV2943232	single nucleotide variant	NM_001039660.2(IL18BP):c.359+11C>T	not provided [RCV003664990]	uncertain significance	11	72001335	72001335	Human		name
405150762	CV2959680	single nucleotide variant	NM_001039660.2(IL18BP):c.508-16G>A	not provided [RCV003673958]	likely benign	11	72001768	72001768	Human		name
405203408	CV2986092	single nucleotide variant	NM_001039660.2(IL18BP):c.507+14G>A	not provided [RCV003678429]	uncertain significance	11	72001566	72001566	Human		name
405182816	CV3031885	single nucleotide variant	NM_001039660.2(IL18BP):c.236-10G>T	not provided [RCV003705711]	likely benign	11	72001191	72001191	Human		name
405226601	CV3039430	single nucleotide variant	NM_001039660.2(IL18BP):c.359+10G>T	not provided [RCV003710812]	likely benign	11	72001334	72001334	Human		name
597952677	CV3798812	single nucleotide variant	NM_001039660.2(IL18BP):c.507+15G>A	not provided [RCV005136386]	likely benign	11	72001567	72001567	Human		name
597961456	CV3812152	single nucleotide variant	NM_001039660.2(IL18BP):c.235+16G>A	not provided [RCV005163805]	likely benign	11	72000573	72000573	Human		name
150339095	CV1108820	single nucleotide variant	NM_001393487.1(IL18RAP):c.579+293T>C	Ascending aortic dissection [RCV001543137]	association	2	102424707	102424707	Human	2	name
150339096	CV1108821	single nucleotide variant	NM_001393487.1(IL18RAP):c.920+241T>A	Ascending aortic dissection [RCV001543138]	association	2	102443564	102443564	Human	2	name
14976042	CV677012	deletion	NM_001039660.2(IL18BP):c.508-19_528del	Hepatitis, fulminant viral, susceptibility to [RCV000850134]	risk factor	11	72001760	72001799	Human	1	name
156030064	CV2022617	deletion	NM_001039660.2(IL18BP):c.235+12_235+14del	not provided [RCV002735771]	benign	11	72000569	72000571	Human		name
156023151	CV2145425	indel	NM_001039660.2(IL18BP):c.28+18_28+19delinsAT	not provided [RCV003018327]	uncertain significance	11	72000030	72000031	Human		name
405091363	CV2878057	indel	NM_001039660.2(IL18BP):c.359+9_359+10delinsGCTCCCAACCCGACCCTGGGAACCTCTGTGCCCATAGCCCACCCTCCACCACTGTGCTTCTTACTCAGTGGCACTTCCACCTCTGGCCAGGTCACTTCCAATGCTGGACACTGCTTAGCTGCTGGGAACACTGGGGGCTGGGAGGGGCAGGGGTCCTTTGTGCTTCTAACTGAGGCAGTGGCAGCTGTGGTGGTCTGCGAGACAGGTGTGGCTCTGACC ... (more) AGGAGAGTGACGACGTGGGCACACAGGAGCAGGACCCACAAAGGGCTGAGGTCTGAGGAAAGGA	not provided [RCV003549925]	uncertain significance	11	72001333	72001334	Human		name
15132971	CV707634	single nucleotide variant	NM_003855.5(IL18R1):c.21C>G (p.Pro7=)	not provided [RCV000964869]	benign	2	102362681	102362681	Human		name
155971600	CV2334235	single nucleotide variant	NM_003855.5(IL18R1):c.42A>G (p.Ile14Met)	not specified [RCV004186219]	likely benign	2	102362702	102362702	Human		name
405804767	CV3271008	single nucleotide variant	NM_003855.5(IL18R1):c.34G>C (p.Val12Leu)	not specified [RCV004405069]	uncertain significance	2	102362694	102362694	Human		name
155960120	CV2023558	single nucleotide variant	NM_001039660.2(IL18BP):c.54C>A (p.Leu18=)	not provided [RCV002731134]	likely benign\|uncertain significance	11	72000376	72000376	Human		name
156287324	CV2058141	single nucleotide variant	NM_001039660.2(IL18BP):c.30C>T (p.Asp10=)	not provided [RCV002833057]	likely benign\|uncertain significance	11	72000352	72000352	Human		name
156336865	CV2110151	single nucleotide variant	NM_001039660.2(IL18BP):c.54C>T (p.Leu18=)	not provided [RCV002938686]	benign	11	72000376	72000376	Human		name
156195969	CV2171546	single nucleotide variant	NM_001039660.2(IL18BP):c.69C>T (p.Val23=)	not provided [RCV003024287]	uncertain significance	11	72000391	72000391	Human		name
156402583	CV2189464	single nucleotide variant	NM_001039660.2(IL18BP):c.96T>A (p.Pro32=)	not provided [RCV003052448]	likely benign\|uncertain significance	11	72000418	72000418	Human		name
402478141	CV2854493	single nucleotide variant	NM_001039660.2(IL18BP):c.51G>A (p.Leu17=)	not provided [RCV003543709]	likely benign	11	72000373	72000373	Human		name
405241069	CV2970650	single nucleotide variant	NM_001039660.2(IL18BP):c.7A>G (p.Met3Val)	not provided [RCV003684055]	uncertain significance	11	71999991	71999991	Human		name
405246868	CV3048116	single nucleotide variant	NM_001039660.2(IL18BP):c.69C>A (p.Val23=)	not provided [RCV003720546]	uncertain significance	11	72000391	72000391	Human		name
405221424	CV3060200	single nucleotide variant	NM_001039660.2(IL18BP):c.66C>T (p.His22=)	not provided [RCV003733372]	likely benign\|uncertain significance	11	72000388	72000388	Human		name
407515718	CV3444527	single nucleotide variant	NM_003855.5(IL18R1):c.112C>G (p.Leu38Val)	not specified [RCV004627978]	uncertain significance	2	102367878	102367878	Human		name
597793107	CV3686376	single nucleotide variant	NM_003855.5(IL18R1):c.144G>C (p.Glu48Asp)	not specified [RCV004934095]	uncertain significance	2	102367910	102367910	Human		name
597793110	CV3686377	single nucleotide variant	NM_003855.5(IL18R1):c.289T>C (p.Phe97Leu)	not specified [RCV004934096]	uncertain significance	2	102368055	102368055	Human		name
597793113	CV3686378	single nucleotide variant	NM_003855.5(IL18R1):c.287A>G (p.Tyr96Cys)	not specified [RCV004934097]	uncertain significance	2	102368053	102368053	Human		name
597793116	CV3686379	single nucleotide variant	NM_003855.5(IL18R1):c.169T>C (p.Tyr57His)	not specified [RCV004934098]	uncertain significance	2	102367935	102367935	Human		name
597793119	CV3686380	single nucleotide variant	NM_003855.5(IL18R1):c.165C>A (p.Ser55Arg)	not specified [RCV004934099]	likely benign	2	102367931	102367931	Human		name
597870342	CV3799792	single nucleotide variant	NM_001039660.2(IL18BP):c.33C>T (p.Leu11=)	not provided [RCV005148206]	likely benign	11	72000355	72000355	Human		name
8625085	CV80204	single nucleotide variant	NM_003853.3(IL18RAP):c.41G>A (p.Gly14Glu)	Malignant melanoma [RCV000060280]	not provided	2	102423318	102423318	Human		name
8625086	CV80205	single nucleotide variant	NM_003853.3(IL18RAP):c.354G>A (p.Val118=)	Malignant melanoma [RCV000060281]	not provided	2	102424094	102424094	Human		name
156376360	CV1917671	single nucleotide variant	NM_001039660.2(IL18BP):c.261G>A (p.Val87=)	not provided [RCV002603615]	likely benign\|uncertain significance	11	72001226	72001226	Human		name
156130723	CV2022726	single nucleotide variant	NM_001039660.2(IL18BP):c.138C>T (p.Ser46=)	not provided [RCV002740554]	uncertain significance	11	72000460	72000460	Human		name
156296595	CV2073528	single nucleotide variant	NM_001039660.2(IL18BP):c.108C>G (p.Thr36=)	not provided [RCV002833428]	uncertain significance	11	72000430	72000430	Human		name
156309132	CV2123305	single nucleotide variant	NM_001039660.2(IL18BP):c.102G>A (p.Ser34=)	not provided [RCV002962516]	likely benign\|uncertain significance	11	72000424	72000424	Human		name
156395114	CV2325113	single nucleotide variant	NM_003855.5(IL18R1):c.754G>A (p.Gly252Arg)	not specified [RCV004175642]	uncertain significance	2	102384943	102384943	Human		name
156037389	CV2374068	single nucleotide variant	NM_003855.5(IL18R1):c.628C>T (p.Arg210Cys)	not specified [RCV004227190]	uncertain significance	2	102381622	102381622	Human		name
401744480	CV2688171	single nucleotide variant	NM_003855.5(IL18R1):c.628C>G (p.Arg210Gly)	not specified [RCV004305214]	uncertain significance	2	102381622	102381622	Human		name
401778178	CV2718549	single nucleotide variant	NM_003855.5(IL18R1):c.908C>T (p.Thr303Met)	not specified [RCV004318350]	uncertain significance	2	102386959	102386959	Human		name
401763625	CV2720392	single nucleotide variant	NM_003855.5(IL18R1):c.939G>C (p.Leu313Phe)	not specified [RCV004325700]	uncertain significance	2	102386990	102386990	Human		name
405216207	CV2876300	single nucleotide variant	NM_001039660.2(IL18BP):c.279C>G (p.Pro93=)	not provided [RCV003553228]	uncertain significance	11	72001244	72001244	Human		name
405143506	CV3027210	single nucleotide variant	NM_001039660.2(IL18BP):c.168A>C (p.Pro56=)	not provided [RCV003702724]	uncertain significance	11	72000490	72000490	Human		name
405218432	CV3034883	single nucleotide variant	NM_001039660.2(IL18BP):c.26C>G (p.Pro9Arg)	not provided [RCV003709626]\|not specified [RCV005353239]	uncertain significance	11	72000010	72000010	Human		name
405201495	CV3041391	single nucleotide variant	NM_001039660.2(IL18BP):c.273C>A (p.Arg91=)	not provided [RCV003707486]	uncertain significance	11	72001238	72001238	Human		name
402474194	CV3182708	single nucleotide variant	NM_001039660.2(IL18BP):c.165C>T (p.Pro55=)	not provided [RCV003874951]	likely benign	11	72000487	72000487	Human		name
405804565	CV3271009	single nucleotide variant	NM_003855.5(IL18R1):c.476A>T (p.Lys159Ile)	not specified [RCV004405070]	uncertain significance	2	102375914	102375914	Human		name
405804567	CV3271010	single nucleotide variant	NM_003855.5(IL18R1):c.667A>C (p.Asn223His)	not specified [RCV004405071]	uncertain significance	2	102381661	102381661	Human		name
407515721	CV3444528	single nucleotide variant	NM_003855.5(IL18R1):c.967C>T (p.Pro323Ser)	not specified [RCV004627979]	uncertain significance	2	102390073	102390073	Human		name
597793122	CV3686382	single nucleotide variant	NM_003855.5(IL18R1):c.434A>G (p.Tyr145Cys)	not specified [RCV004934100]	uncertain significance	2	102372084	102372084	Human		name
597793125	CV3686383	single nucleotide variant	NM_003855.5(IL18R1):c.966C>G (p.Ile322Met)	not specified [RCV004934101]	uncertain significance	2	102390072	102390072	Human		name
597793104	CV3690253	single nucleotide variant	NM_003855.5(IL18R1):c.702G>C (p.Arg234Ser)	not specified [RCV004934094]	uncertain significance	2	102384891	102384891	Human		name
597943705	CV3847747	single nucleotide variant	NM_001039660.2(IL18BP):c.19T>C (p.Trp7Arg)	not provided [RCV005188475]\|not specified [RCV005353448]	uncertain significance	11	72000003	72000003	Human		name
597900974	CV3855128	single nucleotide variant	NM_001039660.2(IL18BP):c.26C>A (p.Pro9Gln)	not provided [RCV005202036]	uncertain significance	11	72000010	72000010	Human		name
598207367	CV3972152	single nucleotide variant	NM_003855.5(IL18R1):c.393A>T (p.Glu131Asp)	not specified [RCV005337963]	uncertain significance	2	102372043	102372043	Human		name
15161380	CV707635	single nucleotide variant	NM_003855.5(IL18R1):c.509C>T (p.Thr170Met)	not provided [RCV000970078]	benign	2	102375947	102375947	Human		name
156449093	CV1944348	single nucleotide variant	NM_001039660.2(IL18BP):c.486C>T (p.His162=)	not provided [RCV003121205]	likely benign\|uncertain significance	11	72001531	72001531	Human		name
156134264	CV1962845	single nucleotide variant	NM_001039660.2(IL18BP):c.420C>T (p.Thr140=)	not provided [RCV002572340]	likely benign	11	72001465	72001465	Human		name
156109202	CV2002202	single nucleotide variant	NM_001039660.2(IL18BP):c.489C>T (p.Val163=)	not provided [RCV002639871]	likely benign\|uncertain significance	11	72001534	72001534	Human		name
156175167	CV2026696	single nucleotide variant	NM_001039660.2(IL18BP):c.31C>T (p.Leu11Phe)	not provided [RCV002765439]\|not specified [RCV004067838]	uncertain significance	11	72000353	72000353	Human		name
156033568	CV2029895	single nucleotide variant	NM_001039660.2(IL18BP):c.528G>A (p.Leu176=)	not provided [RCV002735904]	likely benign\|uncertain significance	11	72001804	72001804	Human		name
155982764	CV2088919	single nucleotide variant	NM_001039660.2(IL18BP):c.561C>T (p.His187=)	not provided [RCV002863849]	uncertain significance	11	72001837	72001837	Human		name
156255457	CV2098223	single nucleotide variant	NM_001039660.2(IL18BP):c.64C>A (p.His22Asn)	not provided [RCV002895400]	uncertain significance	11	72000386	72000386	Human		name
156132988	CV2113121	single nucleotide variant	NM_001039660.2(IL18BP):c.70G>A (p.Val24Ile)	not provided [RCV002928272]\|not specified [RCV004067147]	likely benign\|uncertain significance	11	72000392	72000392	Human		name
156357887	CV2126205	single nucleotide variant	NM_001039660.2(IL18BP):c.474T>C (p.Val158=)	not provided [RCV002966788]	likely benign\|uncertain significance	11	72001519	72001519	Human		name
156022047	CV2184619	deletion	NM_001039660.2(IL18BP):c.223del (p.Glu75fs)	not provided [RCV003035778]	uncertain significance	11	72000544	72000544	Human		name
156044813	CV2186372	deletion	NM_001039660.2(IL18BP):c.6_8del (p.Met3del)	not provided [RCV003036704]	uncertain significance	11	71999990	71999992	Human		name
156386537	CV2225124	single nucleotide variant	NM_003855.5(IL18R1):c.1384G>A (p.Glu462Lys)	not specified [RCV004094937]	uncertain significance	2	102396644	102396644	Human		name
156087858	CV2290626	single nucleotide variant	NM_003855.5(IL18R1):c.1471C>G (p.Leu491Val)	not specified [RCV004149163]	uncertain significance	2	102396731	102396731	Human		name
156080975	CV2301044	single nucleotide variant	NM_003855.5(IL18R1):c.1408A>G (p.Lys470Glu)	not specified [RCV004158196]	uncertain significance	2	102396668	102396668	Human		name
156202896	CV2313256	single nucleotide variant	NM_001039660.2(IL18BP):c.70G>C (p.Val24Leu)	not specified [RCV004161505]	uncertain significance	11	72000392	72000392	Human		name
402489954	CV2867077	single nucleotide variant	NM_001039660.2(IL18BP):c.62C>T (p.Ala21Val)	not provided [RCV003544852]	uncertain significance	11	72000384	72000384	Human		name
402521741	CV2867347	single nucleotide variant	NM_001039660.2(IL18BP):c.567T>C (p.Ser189=)	not provided [RCV003547745]	likely benign	11	72001843	72001843	Human		name
402466298	CV2914708	single nucleotide variant	NM_001039660.2(IL18BP):c.432C>T (p.His144=)	not provided [RCV003569419]	uncertain significance	11	72001477	72001477	Human		name
405203767	CV2915161	single nucleotide variant	NM_001039660.2(IL18BP):c.41T>C (p.Leu14Ser)	not provided [RCV003566155]\|not specified [RCV004634293]	uncertain significance	11	72000363	72000363	Human		name
402507254	CV2947806	single nucleotide variant	NM_001039660.2(IL18BP):c.447C>G (p.Ser149=)	not provided [RCV003662138]	uncertain significance	11	72001492	72001492	Human		name
405173274	CV2955391	single nucleotide variant	NM_001039660.2(IL18BP):c.459G>A (p.Val153=)	not provided [RCV003675608]	uncertain significance	11	72001504	72001504	Human		name
405193862	CV2975162	single nucleotide variant	NM_001039660.2(IL18BP):c.76C>T (p.Leu26Phe)	not provided [RCV003677457]	uncertain significance	11	72000398	72000398	Human		name
402495560	CV3005726	single nucleotide variant	NM_001039660.2(IL18BP):c.357C>G (p.Thr119=)	not provided [RCV003687976]	uncertain significance	11	72001322	72001322	Human		name
405072963	CV3034535	single nucleotide variant	NM_001039660.2(IL18BP):c.534C>G (p.Pro178=)	not provided [RCV003698429]	uncertain significance	11	72001810	72001810	Human		name
405186617	CV3040485	single nucleotide variant	NM_001039660.2(IL18BP):c.456C>T (p.Leu152=)	not provided [RCV003706029]	likely benign	11	72001501	72001501	Human		name
405804559	CV3271006	single nucleotide variant	NM_001039660.2(IL18BP):c.36C>A (p.Ser12Arg)	not specified [RCV004405067]	uncertain significance	11	72000358	72000358	Human		name
405804561	CV3271007	single nucleotide variant	NM_003855.5(IL18R1):c.1354G>T (p.Val452Phe)	not specified [RCV004405068]	uncertain significance	2	102396614	102396614	Human		name
597793128	CV3686384	single nucleotide variant	NM_003855.5(IL18R1):c.1334A>C (p.Lys445Thr)	not specified [RCV004934102]	uncertain significance	2	102396594	102396594	Human		name
597793099	CV3690251	single nucleotide variant	NM_001039660.2(IL18BP):c.42G>C (p.Leu14Phe)	not specified [RCV004934092]	uncertain significance	11	72000364	72000364	Human		name
597957060	CV3754770	single nucleotide variant	NM_001039660.2(IL18BP):c.94C>T (p.Pro32Ser)	not provided [RCV005080620]	uncertain significance	11	72000416	72000416	Human		name
597915864	CV3789118	single nucleotide variant	NM_001039660.2(IL18BP):c.50T>A (p.Leu17Gln)	not provided [RCV005129415]	uncertain significance	11	72000372	72000372	Human		name
597910863	CV3806682	single nucleotide variant	NM_001039660.2(IL18BP):c.390G>A (p.Leu130=)	not provided [RCV005154249]	likely benign	11	72001435	72001435	Human		name
597858608	CV3822299	single nucleotide variant	NM_001039660.2(IL18BP):c.384G>A (p.Thr128=)	not provided [RCV005174597]	likely benign	11	72001429	72001429	Human		name
597976423	CV3829608	single nucleotide variant	NM_001039660.2(IL18BP):c.339A>G (p.Arg113=)	not provided [RCV005169875]	likely benign	11	72001304	72001304	Human		name
597859758	CV3832940	single nucleotide variant	NM_001039660.2(IL18BP):c.74C>G (p.Thr25Ser)	not provided [RCV005174853]	uncertain significance	11	72000396	72000396	Human		name
597895831	CV3834518	single nucleotide variant	NM_001039660.2(IL18BP):c.534C>T (p.Pro178=)	not provided [RCV005180429]	likely benign	11	72001810	72001810	Human		name
597925809	CV3840601	single nucleotide variant	NM_001039660.2(IL18BP):c.61G>A (p.Ala21Thr)	not provided [RCV005185072]	uncertain significance	11	72000383	72000383	Human		name
598179645	CV3972151	single nucleotide variant	NM_003855.5(IL18R1):c.1281T>A (p.Asp427Glu)	not specified [RCV005352197]	uncertain significance	2	102396541	102396541	Human		name
598207372	CV3972153	single nucleotide variant	NM_003855.5(IL18R1):c.1259T>C (p.Val420Ala)	not specified [RCV005337964]	uncertain significance	2	102394616	102394616	Human		name
15196263	CV724699	single nucleotide variant	NM_001039660.2(IL18BP):c.67G>A (p.Val23Ile)	Hepatitis, fulminant viral, susceptibility to [RCV002495383]\|not provided [RCV000889729]	likely benign	11	72000389	72000389	Human	1	name
8625087	CV80206	single nucleotide variant	NM_003853.3(IL18RAP):c.943G>A (p.Glu315Lys)	Malignant melanoma [RCV000060282]	not provided	2	102445211	102445211	Human		name
156351324	CV1883036	single nucleotide variant	NM_001039660.2(IL18BP):c.190T>G (p.Cys64Gly)	not provided [RCV003090998]	uncertain significance	11	72000512	72000512	Human		name
156296855	CV1894403	single nucleotide variant	NM_001039660.2(IL18BP):c.269G>C (p.Ser90Thr)	not provided [RCV003087730]	uncertain significance	11	72001234	72001234	Human		name
155927005	CV1901782	single nucleotide variant	NM_001039660.2(IL18BP):c.232C>G (p.Leu78Val)	not provided [RCV002614815]	likely benign	11	72000554	72000554	Human		name
156044247	CV1927026	single nucleotide variant	NM_001039660.2(IL18BP):c.178G>T (p.Ala60Ser)	not provided [RCV002637700]	uncertain significance	11	72000500	72000500	Human		name
156260379	CV2033930	single nucleotide variant	NM_001039660.2(IL18BP):c.188A>C (p.Gln63Pro)	not provided [RCV002746287]	uncertain significance	11	72000510	72000510	Human		name
155969881	CV2062400	single nucleotide variant	NM_001039660.2(IL18BP):c.146A>T (p.Asp49Val)	not provided [RCV002842028]	uncertain significance	11	72000468	72000468	Human		name
155908488	CV2077603	single nucleotide variant	NM_001039660.2(IL18BP):c.191G>T (p.Cys64Phe)	not provided [RCV002858307]	uncertain significance	11	72000513	72000513	Human		name
156006900	CV2099798	single nucleotide variant	NM_001039660.2(IL18BP):c.101C>T (p.Ser34Leu)	not provided [RCV002908899]	likely benign	11	72000423	72000423	Human		name
156342747	CV2103515	single nucleotide variant	NM_001039660.2(IL18BP):c.271C>T (p.Arg91Cys)	not provided [RCV002900569]\|not specified [RCV004632092]	uncertain significance	11	72001236	72001236	Human		name
156024750	CV2106029	single nucleotide variant	NM_001039660.2(IL18BP):c.272G>A (p.Arg91His)	not provided [RCV002923237]\|not specified [RCV004067126]	uncertain significance	11	72001237	72001237	Human		name
156251129	CV2130120	single nucleotide variant	NM_001039660.2(IL18BP):c.106A>G (p.Thr36Ala)	not provided [RCV002959213]	uncertain significance	11	72000428	72000428	Human		name
156364835	CV2130532	single nucleotide variant	NM_001039660.2(IL18BP):c.242C>T (p.Thr81Met)	not provided [RCV002967226]\|not specified [RCV004632123]	uncertain significance	11	72001207	72001207	Human		name
156170445	CV2133546	single nucleotide variant	NM_001039660.2(IL18BP):c.233T>A (p.Leu78Gln)	not provided [RCV003005370]	uncertain significance	11	72000555	72000555	Human		name
156204163	CV2134877	single nucleotide variant	NM_001039660.2(IL18BP):c.205G>T (p.Val69Leu)	not provided [RCV002985334]	uncertain significance	11	72000527	72000527	Human		name
156036699	CV2243627	single nucleotide variant	NM_001393487.1(IL18RAP):c.82A>G (p.Lys28Glu)	not specified [RCV004114347]	uncertain significance	2	102423822	102423822	Human		name
156318086	CV2251138	single nucleotide variant	NM_001039660.2(IL18BP):c.121A>G (p.Thr41Ala)	not provided [RCV005099695]\|not specified [RCV004123672]	uncertain significance	11	72000443	72000443	Human		name
155958609	CV2313815	single nucleotide variant	NM_001393487.1(IL18RAP):c.97A>G (p.Thr33Ala)	not specified [RCV004164141]	likely benign	2	102423837	102423837	Human		name
156243009	CV2347044	single nucleotide variant	NM_001393487.1(IL18RAP):c.37G>T (p.Ala13Ser)	not specified [RCV004204528]	likely benign	2	102423314	102423314	Human		name
401770301	CV2715124	single nucleotide variant	NM_001039660.2(IL18BP):c.176C>T (p.Pro59Leu)	not specified [RCV004322699]	uncertain significance	11	72000498	72000498	Human		name
405101658	CV2948206	duplication	NM_001039660.2(IL18BP):c.534dup (p.Thr179fs)	not provided [RCV003666163]	uncertain significance	11	72001804	72001805	Human		name
405173928	CV2955480	single nucleotide variant	NM_001039660.2(IL18BP):c.169G>C (p.Val57Leu)	not provided [RCV003675663]	uncertain significance	11	72000491	72000491	Human		name
402507179	CV2978793	deletion	NM_001039660.2(IL18BP):c.19_20del (p.Trp7fs)	not provided [RCV003689174]	uncertain significance	11	72000003	72000004	Human		name
405236839	CV3032902	single nucleotide variant	NM_001039660.2(IL18BP):c.253T>C (p.Ser85Pro)	not provided [RCV003712505]	uncertain significance	11	72001218	72001218	Human		name
405196876	CV3037806	single nucleotide variant	NM_001039660.2(IL18BP):c.239G>A (p.Gly80Glu)	not provided [RCV003707016]	uncertain significance	11	72001204	72001204	Human		name
405240547	CV3060710	single nucleotide variant	NM_001039660.2(IL18BP):c.272G>T (p.Arg91Leu)	not provided [RCV003737106]\|not specified [RCV004927942]	uncertain significance	11	72001237	72001237	Human		name
402521503	CV3179535	single nucleotide variant	NM_001039660.2(IL18BP):c.194C>T (p.Pro65Leu)	not provided [RCV003879787]	uncertain significance	11	72000516	72000516	Human		name
597793102	CV3690252	single nucleotide variant	NM_001039660.2(IL18BP):c.212G>C (p.Trp71Ser)	not specified [RCV004934093]	uncertain significance	11	72000534	72000534	Human		name
597891016	CV3762944	single nucleotide variant	NM_001039660.2(IL18BP):c.154C>A (p.Pro52Thr)	not provided [RCV005110717]	uncertain significance	11	72000476	72000476	Human		name
597860211	CV3770056	single nucleotide variant	NM_001039660.2(IL18BP):c.262G>A (p.Ala88Thr)	not provided [RCV005105908]	uncertain significance	11	72001227	72001227	Human		name
597898715	CV3782604	single nucleotide variant	NM_001039660.2(IL18BP):c.100T>G (p.Ser34Ala)	not provided [RCV005126829]	uncertain significance	11	72000422	72000422	Human		name
597888807	CV3804765	single nucleotide variant	NM_001039660.2(IL18BP):c.202G>T (p.Glu68Ter)	not provided [RCV005151027]	uncertain significance	11	72000524	72000524	Human		name
597938966	CV3808355	single nucleotide variant	NM_001039660.2(IL18BP):c.290T>A (p.Ile97Asn)	not provided [RCV005158543]	uncertain significance	11	72001255	72001255	Human		name
598179662	CV3972158	single nucleotide variant	NM_001393487.1(IL18RAP):c.34G>T (p.Val12Phe)	not specified [RCV005352200]	uncertain significance	2	102423311	102423311	Human		name
15168326	CV746719	single nucleotide variant	NM_001393487.1(IL18RAP):c.618C>T (p.Ile206=)	not provided [RCV000927268]	likely benign	2	102437250	102437250	Human		name
156194526	CV1889452	single nucleotide variant	NM_001039660.2(IL18BP):c.320T>C (p.Ile107Thr)	not provided [RCV003083987]\|not specified [RCV004071799]	uncertain significance	11	72001285	72001285	Human		name
155955529	CV1907179	single nucleotide variant	NM_001039660.2(IL18BP):c.457G>A (p.Val153Met)	not provided [RCV003095564]	uncertain significance	11	72001502	72001502	Human		name
156418469	CV1911151	single nucleotide variant	NM_001039660.2(IL18BP):c.367C>T (p.Arg123Cys)	not provided [RCV002611664]\|not specified [RCV004927891]	uncertain significance	11	72001412	72001412	Human		name
156194013	CV1912183	single nucleotide variant	NM_001039660.2(IL18BP):c.490G>A (p.Val164Ile)	not provided [RCV002595469]	uncertain significance	11	72001535	72001535	Human		name
156201660	CV1925635	single nucleotide variant	NM_001039660.2(IL18BP):c.499C>G (p.Gln167Glu)	not provided [RCV002643653]	uncertain significance	11	72001544	72001544	Human		name
156063464	CV1925774	single nucleotide variant	NM_001039660.2(IL18BP):c.444C>A (p.Phe148Leu)	not provided [RCV002621025]	uncertain significance	11	72001489	72001489	Human		name
156147556	CV1932302	single nucleotide variant	NM_001039660.2(IL18BP):c.368G>A (p.Arg123His)	not provided [RCV002623888]	uncertain significance	11	72001413	72001413	Human		name
156434739	CV1940178	single nucleotide variant	NM_001039660.2(IL18BP):c.350G>A (p.Gly117Glu)	not provided [RCV003104594]	uncertain significance	11	72001315	72001315	Human		name
156030034	CV2022614	single nucleotide variant	NM_001039660.2(IL18BP):c.554C>A (p.Ser185Tyr)	not provided [RCV002735770]	uncertain significance	11	72001830	72001830	Human		name
156130857	CV2022733	single nucleotide variant	NM_001039660.2(IL18BP):c.576G>T (p.Gln192His)	not provided [RCV002740558]	benign	11	72001852	72001852	Human		name
156097287	CV2027174	single nucleotide variant	NM_001039660.2(IL18BP):c.530C>A (p.Pro177His)	not provided [RCV002761177]	uncertain significance	11	72001806	72001806	Human		name
156052145	CV2027390	single nucleotide variant	NM_001039660.2(IL18BP):c.523A>G (p.Thr175Ala)	not provided [RCV002736546]	uncertain significance	11	72001799	72001799	Human		name
156094538	CV2030815	single nucleotide variant	NM_001039660.2(IL18BP):c.551C>T (p.Pro184Leu)	not provided [RCV002761074]	uncertain significance	11	72001827	72001827	Human		name
155938364	CV2041409	single nucleotide variant	NM_001039660.2(IL18BP):c.383C>T (p.Thr128Met)	not provided [RCV002775030]	uncertain significance	11	72001428	72001428	Human		name
156126712	CV2046853	single nucleotide variant	NM_001039660.2(IL18BP):c.304G>A (p.Gly102Ser)	not provided [RCV002800450]\|not specified [RCV004064713]	uncertain significance	11	72001269	72001269	Human		name
156350099	CV2122055	single nucleotide variant	NM_001039660.2(IL18BP):c.440A>G (p.Asn147Ser)	not provided [RCV002966234]	benign	11	72001485	72001485	Human		name
156304523	CV2129684	single nucleotide variant	NM_001039660.2(IL18BP):c.482G>A (p.Arg161His)	not provided [RCV002962299]	uncertain significance	11	72001527	72001527	Human		name
156083097	CV2144589	single nucleotide variant	NM_001039660.2(IL18BP):c.388C>G (p.Leu130Val)	not provided [RCV003020416]	uncertain significance	11	72001433	72001433	Human		name
156315131	CV2158561	single nucleotide variant	NM_001039660.2(IL18BP):c.487G>A (p.Val163Ile)	not provided [RCV003028813]\|not specified [RCV004068607]	uncertain significance	11	72001532	72001532	Human		name
156266224	CV2170187	single nucleotide variant	NM_001039660.2(IL18BP):c.361C>T (p.Arg121Trp)	not provided [RCV003026828]\|not specified [RCV004068626]	uncertain significance	11	72001406	72001406	Human		name
156174479	CV2326944	single nucleotide variant	NM_001039660.2(IL18BP):c.403G>A (p.Val135Met)	not specified [RCV004176755]	uncertain significance	11	72001448	72001448	Human		name
329397456	CV2456191	single nucleotide variant	NM_001039660.2(IL18BP):c.364G>A (p.Glu122Lys)	not specified [RCV004273379]	uncertain significance	11	72001409	72001409	Human		name
401778943	CV2701903	single nucleotide variant	NM_001039660.2(IL18BP):c.482G>T (p.Arg161Leu)	not specified [RCV004320520]	uncertain significance	11	72001527	72001527	Human		name
405220176	CV2904171	single nucleotide variant	NM_001039660.2(IL18BP):c.449G>A (p.Cys150Tyr)	not provided [RCV003568310]	uncertain significance	11	72001494	72001494	Human		name
405010732	CV2933626	single nucleotide variant	NM_001039660.2(IL18BP):c.325C>G (p.His109Asp)	not provided [RCV003576710]	uncertain significance	11	72001290	72001290	Human		name
405151062	CV2957054	single nucleotide variant	NM_001039660.2(IL18BP):c.577C>T (p.Gln193Ter)	not provided [RCV003670062]	uncertain significance	11	72001853	72001853	Human		name
405246800	CV2966460	single nucleotide variant	NM_001039660.2(IL18BP):c.542A>C (p.Glu181Ala)	not provided [RCV003685514]	uncertain significance	11	72001818	72001818	Human		name
405219789	CV2969515	single nucleotide variant	NM_001039660.2(IL18BP):c.448T>C (p.Cys150Arg)	not provided [RCV003680505]	uncertain significance	11	72001493	72001493	Human		name
405013593	CV2994168	single nucleotide variant	NM_001039660.2(IL18BP):c.328C>G (p.Leu110Val)	not provided [RCV003694196]	uncertain significance	11	72001293	72001293	Human		name
405045053	CV3017712	single nucleotide variant	NM_001039660.2(IL18BP):c.481C>T (p.Arg161Cys)	not provided [RCV003696597]	uncertain significance	11	72001526	72001526	Human		name
405092749	CV3025990	single nucleotide variant	NM_001039660.2(IL18BP):c.532C>T (p.Pro178Ser)	not provided [RCV003699796]	uncertain significance	11	72001808	72001808	Human		name
405126552	CV3031224	single nucleotide variant	NM_001039660.2(IL18BP):c.524C>T (p.Thr175Ile)	not provided [RCV003701221]	uncertain significance	11	72001800	72001800	Human		name
405074944	CV3034721	single nucleotide variant	NM_001039660.2(IL18BP):c.473T>C (p.Val158Ala)	not provided [RCV003698542]	uncertain significance	11	72001518	72001518	Human		name
402512369	CV3042662	single nucleotide variant	NM_001039660.2(IL18BP):c.565A>G (p.Ser189Gly)	not provided [RCV003715722]	uncertain significance	11	72001841	72001841	Human		name
405046531	CV3071659	single nucleotide variant	NM_001039660.2(IL18BP):c.338G>A (p.Arg113Gln)	not provided [RCV003740291]	uncertain significance	11	72001303	72001303	Human		name
407515736	CV3444532	single nucleotide variant	NM_001393487.1(IL18RAP):c.144A>C (p.Leu48Phe)	not specified [RCV004627983]	uncertain significance	2	102423884	102423884	Human		name
407515754	CV3444537	single nucleotide variant	NM_001393487.1(IL18RAP):c.168C>A (p.Phe56Leu)	not specified [RCV004627988]	uncertain significance	2	102423908	102423908	Human		name
597906220	CV3803936	single nucleotide variant	NM_001039660.2(IL18BP):c.362G>T (p.Arg121Leu)	not provided [RCV005153481]	uncertain significance	11	72001407	72001407	Human		name
597959879	CV3811519	single nucleotide variant	NM_001039660.2(IL18BP):c.485A>C (p.His162Pro)	not provided [RCV005163366]	uncertain significance	11	72001530	72001530	Human		name
597863334	CV3814013	single nucleotide variant	NM_001039660.2(IL18BP):c.308A>G (p.Asn103Ser)	not provided [RCV005147082]	uncertain significance	11	72001273	72001273	Human		name
597967011	CV3820329	single nucleotide variant	NM_001039660.2(IL18BP):c.410A>G (p.Glu137Gly)	not provided [RCV005165366]	uncertain significance	11	72001455	72001455	Human		name
597897961	CV3826565	single nucleotide variant	NM_001039660.2(IL18BP):c.376A>G (p.Thr126Ala)	not provided [RCV005180698]	uncertain significance	11	72001421	72001421	Human		name
15157164	CV713129	single nucleotide variant	NM_001039660.2(IL18BP):c.362G>A (p.Arg121Gln)	not provided [RCV000969257]	benign	11	72001407	72001407	Human		name
156292359	CV2233445	single nucleotide variant	NM_001393487.1(IL18RAP):c.832G>A (p.Gly278Ser)	not specified [RCV004106071]	uncertain significance	2	102443235	102443235	Human		name
156295390	CV2239665	single nucleotide variant	NM_001393487.1(IL18RAP):c.490G>T (p.Asp164Tyr)	not specified [RCV004108213]	likely benign	2	102424325	102424325	Human		name
156031567	CV2249830	single nucleotide variant	NM_001393487.1(IL18RAP):c.904G>T (p.Val302Leu)	not specified [RCV004122579]	uncertain significance	2	102443307	102443307	Human		name
156131543	CV2279963	single nucleotide variant	NM_001393487.1(IL18RAP):c.953A>G (p.Glu318Gly)	not specified [RCV004146334]	uncertain significance	2	102445221	102445221	Human		name
156082939	CV2333704	single nucleotide variant	NM_001393487.1(IL18RAP):c.773A>G (p.Glu258Gly)	not specified [RCV004192542]	uncertain significance	2	102441354	102441354	Human		name
156270159	CV2398651	single nucleotide variant	NM_001393487.1(IL18RAP):c.619G>A (p.Val207Ile)	not specified [RCV004240000]	uncertain significance	2	102437251	102437251	Human		name
329352369	CV2452923	single nucleotide variant	NM_001393487.1(IL18RAP):c.631G>A (p.Val211Ile)	not specified [RCV004277560]	likely benign	2	102437263	102437263	Human		name
401760024	CV2701841	single nucleotide variant	NM_001393487.1(IL18RAP):c.364G>C (p.Gly122Arg)	not specified [RCV004307806]	uncertain significance	2	102424104	102424104	Human		name
401736080	CV2703037	single nucleotide variant	NM_001393487.1(IL18RAP):c.764A>T (p.Asp255Val)	not specified [RCV004321343]	uncertain significance	2	102441345	102441345	Human		name
401752028	CV2713889	single nucleotide variant	NM_001393487.1(IL18RAP):c.431T>C (p.Ile144Thr)	not specified [RCV004315322]	uncertain significance	2	102424266	102424266	Human		name
401768776	CV2716726	single nucleotide variant	NM_001393487.1(IL18RAP):c.437A>C (p.Glu146Ala)	not specified [RCV004327772]	uncertain significance	2	102424272	102424272	Human		name
405804573	CV3271013	single nucleotide variant	NM_001393487.1(IL18RAP):c.677C>T (p.Ser226Leu)	not specified [RCV004405074]	uncertain significance	2	102437309	102437309	Human		name
405804575	CV3271014	single nucleotide variant	NM_001393487.1(IL18RAP):c.724A>G (p.Thr242Ala)	not specified [RCV004405075]	uncertain significance	2	102437356	102437356	Human		name
405804576	CV3271015	single nucleotide variant	NM_001393487.1(IL18RAP):c.868T>C (p.Tyr290His)	not specified [RCV004405076]	uncertain significance	2	102443271	102443271	Human		name
405804578	CV3271016	single nucleotide variant	NM_001393487.1(IL18RAP):c.962T>A (p.Ile321Asn)	not specified [RCV004405077]	uncertain significance	2	102445230	102445230	Human		name
407515729	CV3444530	single nucleotide variant	NM_001393487.1(IL18RAP):c.614G>A (p.Arg205Gln)	not specified [RCV004627981]	uncertain significance	2	102437246	102437246	Human		name
597793137	CV3686387	single nucleotide variant	NM_001393487.1(IL18RAP):c.692C>T (p.Ser231Leu)	not specified [RCV004934105]	uncertain significance	2	102437324	102437324	Human		name
598179650	CV3972155	single nucleotide variant	NM_001393487.1(IL18RAP):c.949A>T (p.Ile317Phe)	not specified [RCV005352198]	uncertain significance	2	102445217	102445217	Human		name
598179658	CV3972156	single nucleotide variant	NM_001393487.1(IL18RAP):c.334C>A (p.His112Asn)	not specified [RCV005352199]	uncertain significance	2	102424074	102424074	Human		name
598207385	CV3972157	single nucleotide variant	NM_001393487.1(IL18RAP):c.932C>T (p.Thr311Ile)	not specified [RCV005337966]	uncertain significance	2	102445200	102445200	Human		name
156370265	CV2263507	single nucleotide variant	NM_001393487.1(IL18RAP):c.1642A>G (p.Asn548Asp)	not specified [RCV004133739]	uncertain significance	2	102452023	102452023	Human		name
155955827	CV2303956	single nucleotide variant	NM_001393487.1(IL18RAP):c.1541T>A (p.Phe514Tyr)	not specified [RCV004168227]	uncertain significance	2	102451922	102451922	Human		name
155931405	CV2362550	single nucleotide variant	NM_001393487.1(IL18RAP):c.1697G>A (p.Gly566Glu)	not specified [RCV004215212]	uncertain significance	2	102452078	102452078	Human		name
401744692	CV2681104	single nucleotide variant	NM_001393487.1(IL18RAP):c.1487C>G (p.Ala496Gly)	not specified [RCV004296162]	uncertain significance	2	102451868	102451868	Human		name
401888493	CV2761550	single nucleotide variant	NM_001393487.1(IL18RAP):c.1649G>A (p.Arg550Lys)	not specified [RCV004334719]	uncertain significance	2	102452030	102452030	Human		name
405804569	CV3271011	single nucleotide variant	NM_001393487.1(IL18RAP):c.1234G>A (p.Val412Ile)	not specified [RCV004405072]	likely benign	2	102450871	102450871	Human		name
405804571	CV3271012	single nucleotide variant	NM_001393487.1(IL18RAP):c.1724C>T (p.Thr575Ile)	not specified [RCV004405073]	likely benign	2	102452105	102452105	Human		name
407515726	CV3444529	single nucleotide variant	NM_001393487.1(IL18RAP):c.1732A>T (p.Ile578Phe)	not specified [RCV004627980]	likely benign	2	102452113	102452113	Human		name
407515732	CV3444531	single nucleotide variant	NM_001393487.1(IL18RAP):c.1399A>G (p.Ile467Val)	not specified [RCV004627982]	uncertain significance	2	102451780	102451780	Human		name
407515746	CV3444535	single nucleotide variant	NM_001393487.1(IL18RAP):c.1177C>T (p.Arg393Trp)	not specified [RCV004627986]	uncertain significance	2	102447174	102447174	Human		name
407515750	CV3444536	single nucleotide variant	NM_001393487.1(IL18RAP):c.1006G>A (p.Val336Ile)	not specified [RCV004627987]	likely benign	2	102445274	102445274	Human		name
597793131	CV3686385	single nucleotide variant	NM_001393487.1(IL18RAP):c.1296C>A (p.His432Gln)	not specified [RCV004934103]	uncertain significance	2	102450933	102450933	Human		name
597793134	CV3686386	single nucleotide variant	NM_001393487.1(IL18RAP):c.1744A>G (p.Lys582Glu)	not specified [RCV004934104]	uncertain significance	2	102452125	102452125	Human		name
598207378	CV3972154	single nucleotide variant	NM_001393487.1(IL18RAP):c.1672C>T (p.His558Tyr)	not specified [RCV005337965]	uncertain significance	2	102452053	102452053	Human		name
598179668	CV3972159	single nucleotide variant	NM_001393487.1(IL18RAP):c.1208G>C (p.Gly403Ala)	not specified [RCV005352201]	uncertain significance	2	102447205	102447205	Human		name
598179673	CV3972160	single nucleotide variant	NM_001393487.1(IL18RAP):c.1646C>G (p.Ser549Cys)	not specified [RCV005352202]	uncertain significance	2	102452027	102452027	Human		name
598179678	CV3972161	single nucleotide variant	NM_001393487.1(IL18RAP):c.1559C>T (p.Pro520Leu)	not specified [RCV005352203]	uncertain significance	2	102451940	102451940	Human		name
15152394	CV719172	single nucleotide variant	NM_001393487.1(IL18RAP):c.1048G>A (p.Val350Ile)	not provided [RCV000879797]	benign	2	102445316	102445316	Human		name
156447158	CV1944800	deletion	NM_001039660.2(IL18BP):c.355_356del (p.Thr119fs)	not provided [RCV003118685]	uncertain significance	11	72001319	72001320	Human		name
402521015	CV2902821	deletion	NM_001039660.2(IL18BP):c.446_448del (p.Ser149del)	not provided [RCV003575855]	uncertain significance	11	72001489	72001491	Human		name

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