Il10 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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846 records found for search term Il10

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401906851	CV2795732	single nucleotide variant	NM_000572.3(IL10):c.*117T>C	not specified [RCV003397084]	benign	1	206768519	206768519	Human		name
151855155	CV1387337	single nucleotide variant	NM_000572.3(IL10):c.444+6C>T	Inflammatory bowel disease [RCV001958496]	uncertain significance	1	206769823	206769823	Human	2	name
151739047	CV1428960	single nucleotide variant	NM_000572.3(IL10):c.225+6A>G	Inflammatory bowel disease [RCV002022139]\|not provided [RCV004691481]	uncertain significance	1	206771350	206771350	Human	2	name
156379110	CV2028958	single nucleotide variant	NM_000572.3(IL10):c.444+8T>C	Inflammatory bowel disease [RCV002722171]	likely benign	1	206769821	206769821	Human	2	name
156269494	CV2135221	single nucleotide variant	NM_000572.3(IL10):c.378+6T>C	Inflammatory bowel disease [RCV002988769]	uncertain significance	1	206770901	206770901	Human	2	name
405190808	CV2871016	single nucleotide variant	NM_000572.3(IL10):c.166-7C>T	Inflammatory bowel disease [RCV003589924]	likely benign	1	206771422	206771422	Human	2	name
405128345	CV2954821	single nucleotide variant	NM_000572.3(IL10):c.445-8C>T	Inflammatory bowel disease [RCV003753902]	likely benign	1	206768736	206768736	Human	2	name
597866417	CV3791090	deletion	NM_000572.3(IL10):c.445-7del	Inflammatory bowel disease [RCV005141122]	likely benign	1	206768735	206768735	Human	2	name
597928934	CV3853705	single nucleotide variant	NM_000572.3(IL10):c.445-7T>G	Inflammatory bowel disease [RCV005203188]	likely benign	1	206768735	206768735	Human	2	name
15165086	CV743657	single nucleotide variant	NM_000572.3(IL10):c.165+8T>C	Inflammatory bowel disease [RCV000904145]	benign	1	206772263	206772263	Human	2	name
127332113	CV1130823	single nucleotide variant	NM_000572.3(IL10):c.165+20G>A	Inflammatory bowel disease [RCV001489284]	likely benign	1	206772251	206772251	Human	2	name
127303445	CV1153432	single nucleotide variant	NM_000572.3(IL10):c.378+19T>C	Inflammatory bowel disease [RCV001515487]\|not provided [RCV004714237]\|not specified [RCV003399292]	benign	1	206770888	206770888	Human	2	name
127303452	CV1153433	single nucleotide variant	NM_000572.3(IL10):c.225+56A>G	Inflammatory bowel disease [RCV001515488]\|not provided [RCV004714238]\|not specified [RCV003399293]	benign	1	206771300	206771300	Human	2	name
152064576	CV1535828	single nucleotide variant	NM_000572.3(IL10):c.225+17G>A	Inflammatory bowel disease [RCV002168457]	likely benign	1	206771339	206771339	Human	2	name
152100843	CV1568355	single nucleotide variant	NM_000572.3(IL10):c.379-19T>G	Inflammatory bowel disease [RCV002115321]	likely benign	1	206769913	206769913	Human	2	name
152026396	CV1582829	deletion	NM_000572.3(IL10):c.379-10del	Inflammatory bowel disease [RCV002084784]	benign	1	206769904	206769904	Human	2	name
152131899	CV1584990	single nucleotide variant	NM_000572.3(IL10):c.225+18G>A	Inflammatory bowel disease [RCV002082973]	likely benign	1	206771338	206771338	Human	2	name
152028208	CV1586767	single nucleotide variant	NM_000572.3(IL10):c.225+15G>A	Inflammatory bowel disease [RCV002085387]	likely benign	1	206771341	206771341	Human	2	name
152165371	CV1649178	single nucleotide variant	NM_000572.3(IL10):c.166-15T>C	Inflammatory bowel disease [RCV002204230]	benign	1	206771430	206771430	Human	2	name
152069788	CV1660696	single nucleotide variant	NM_000572.3(IL10):c.165+15T>C	Inflammatory bowel disease [RCV002129457]	likely benign	1	206772256	206772256	Human	2	name
155968741	CV2079082	single nucleotide variant	NM_000572.3(IL10):c.166-19C>T	Inflammatory bowel disease [RCV002881383]	likely benign	1	206771434	206771434	Human	2	name
405197407	CV2880576	single nucleotide variant	NM_000572.3(IL10):c.165+14C>T	Inflammatory bowel disease [RCV003590733]	likely benign	1	206772257	206772257	Human	2	name
405186074	CV2918547	single nucleotide variant	NM_000572.3(IL10):c.225+20G>A	Inflammatory bowel disease [RCV003589385]	likely benign	1	206771336	206771336	Human	2	name
405124380	CV2949059	single nucleotide variant	NM_000572.3(IL10):c.378+15A>C	Inflammatory bowel disease [RCV003753459]	likely benign	1	206770892	206770892	Human	2	name
405129732	CV2968144	single nucleotide variant	NM_000572.3(IL10):c.378+16G>C	Inflammatory bowel disease [RCV003754079]	likely benign	1	206770891	206770891	Human	2	name
405145747	CV3126469	single nucleotide variant	NM_000572.3(IL10):c.379-16C>T	Inflammatory bowel disease [RCV003817196]	likely benign	1	206769910	206769910	Human	2	name
405056576	CV3147728	single nucleotide variant	NM_000572.3(IL10):c.379-17T>C	Inflammatory bowel disease [RCV003849958]	likely benign	1	206769911	206769911	Human	2	name
405091041	CV3167902	single nucleotide variant	NM_000572.3(IL10):c.444+20G>A	Inflammatory bowel disease [RCV003852292]	likely benign	1	206769809	206769809	Human	2	name
404978909	CV3176007	single nucleotide variant	NM_000572.3(IL10):c.444+17G>A	Inflammatory bowel disease [RCV003880107]	likely benign	1	206769812	206769812	Human	2	name
597913032	CV3847262	single nucleotide variant	NM_000572.3(IL10):c.165+10A>T	Inflammatory bowel disease [RCV005188182]	likely benign	1	206772261	206772261	Human	2	name
127294417	CV1153431	single nucleotide variant	NM_000572.3(IL10):c.378+284G>T	Inflammatory bowel disease [RCV001511739]\|not provided [RCV004714224]	benign	1	206770623	206770623	Human	7	name
401930976	CV2795638	single nucleotide variant	NM_000572.3(IL10):c.166-101T>G	not specified [RCV003391200]	benign	1	206771516	206771516	Human		name
401931031	CV2795647	single nucleotide variant	NM_000572.3(IL10):c.379-112A>G	not specified [RCV003391209]	benign	1	206770006	206770006	Human		name
127316118	CV1109925	single nucleotide variant	NM_000572.3(IL10):c.6C>T (p.His2=)	Inflammatory bowel disease [RCV001465447]\|not provided [RCV002070280]	likely benign	1	206772430	206772430	Human	2	name
127299577	CV1109924	single nucleotide variant	NM_000572.3(IL10):c.18G>A (p.Leu6=)	Inflammatory bowel disease [RCV001478231]	likely benign	1	206772418	206772418	Human	2	name
597907589	CV3829922	single nucleotide variant	NM_000572.3(IL10):c.12A>G (p.Ser4=)	Inflammatory bowel disease [RCV005182491]	likely benign	1	206772424	206772424	Human	2	name
597907739	CV3830069	single nucleotide variant	NM_000572.3(IL10):c.27C>T (p.Cys9=)	Inflammatory bowel disease [RCV005182638]	likely benign	1	206772409	206772409	Human	2	name
127297455	CV1109923	single nucleotide variant	NM_000572.3(IL10):c.84C>T (p.Asn28=)	Inflammatory bowel disease [RCV001453059]	likely benign	1	206772352	206772352	Human	2	name
152068898	CV1562096	single nucleotide variant	NM_000572.3(IL10):c.30G>C (p.Leu10=)	Inflammatory bowel disease [RCV002169034]	likely benign	1	206772406	206772406	Human	2	name
597915066	CV3846995	single nucleotide variant	NM_000572.3(IL10):c.28C>T (p.Leu10=)	Inflammatory bowel disease [RCV005190166]	likely benign	1	206772408	206772408	Human	2	name
597928097	CV3856272	single nucleotide variant	NM_000572.3(IL10):c.69C>G (p.Gly23=)	Inflammatory bowel disease [RCV005202500]	likely benign	1	206772367	206772367	Human	2	name
15149930	CV732051	single nucleotide variant	NM_000572.3(IL10):c.48G>A (p.Val16=)	Inflammatory bowel disease [RCV001421598]	likely benign	1	206772388	206772388	Human	2	name
127266227	CV1066679	single nucleotide variant	NM_000572.3(IL10):c.297G>A (p.Glu99=)	Inflammatory bowel disease [RCV001403822]	likely benign	1	206770988	206770988	Human	2	name
127244363	CV1066680	single nucleotide variant	NM_000572.3(IL10):c.276G>A (p.Glu92=)	Inflammatory bowel disease [RCV001416327]	likely benign	1	206771009	206771009	Human	2	name
127240406	CV1088409	single nucleotide variant	NM_000572.3(IL10):c.201G>A (p.Lys67=)	Inflammatory bowel disease [RCV001434222]	likely benign	1	206771380	206771380	Human	2	name
127334932	CV1130822	single nucleotide variant	NM_000572.3(IL10):c.255G>A (p.Glu85=)	Inflammatory bowel disease [RCV001491190]	likely benign	1	206771030	206771030	Human	2	name
152155904	CV1585883	single nucleotide variant	NM_000572.3(IL10):c.273G>A (p.Leu91=)	Inflammatory bowel disease [RCV002140164]	likely benign	1	206771012	206771012	Human	2	name
156226669	CV1956742	single nucleotide variant	NM_000572.3(IL10):c.252T>G (p.Ser84=)	Inflammatory bowel disease [RCV002575727]	likely benign	1	206771033	206771033	Human	2	name
156328196	CV1990732	single nucleotide variant	NM_000572.3(IL10):c.261C>T (p.Ile87=)	Inflammatory bowel disease [RCV002630777]	likely benign	1	206771024	206771024	Human	2	name
156046315	CV2093302	single nucleotide variant	NM_000572.3(IL10):c.135A>C (p.Arg45=)	Inflammatory bowel disease [RCV002867628]	likely benign	1	206772301	206772301	Human	2	name
405123441	CV2947193	single nucleotide variant	NM_000572.3(IL10):c.213G>T (p.Leu71=)	Inflammatory bowel disease [RCV003753357]	likely benign	1	206771368	206771368	Human	2	name
597834457	CV3760755	single nucleotide variant	NM_000572.3(IL10):c.193T>C (p.Leu65=)	Inflammatory bowel disease [RCV005085306]	likely benign	1	206771388	206771388	Human	2	name
597886972	CV3812663	single nucleotide variant	NM_000572.3(IL10):c.237T>C (p.Gly79=)	Inflammatory bowel disease [RCV005161937]	likely benign	1	206771048	206771048	Human	2	name
15194502	CV761492	single nucleotide variant	NM_000572.3(IL10):c.228T>C (p.Gly76=)	Inflammatory bowel disease [RCV000933663]	likely benign	1	206771057	206771057	Human	2	name
127269398	CV1066678	single nucleotide variant	NM_000572.3(IL10):c.309A>G (p.Pro103=)	Inflammatory bowel disease [RCV001404669]	likely benign	1	206770976	206770976	Human	2	name
127272216	CV1088406	single nucleotide variant	NM_000572.3(IL10):c.471C>A (p.Ala157=)	Inflammatory bowel disease [RCV001431221]	likely benign	1	206768702	206768702	Human	2	name
127280732	CV1088407	single nucleotide variant	NM_000572.3(IL10):c.393C>T (p.Pro131=)	Inflammatory bowel disease [RCV001446696]	likely benign	1	206769880	206769880	Human	2	name
127274487	CV1088408	single nucleotide variant	NM_000572.3(IL10):c.321G>A (p.Ala107=)	Inflammatory bowel disease [RCV001431970]	likely benign	1	206770964	206770964	Human	2	name
127316826	CV1130821	single nucleotide variant	NM_000572.3(IL10):c.375C>A (p.Arg125=)	Inflammatory bowel disease [RCV001482986]	likely benign	1	206770910	206770910	Human	2	name
150528436	CV1288311	single nucleotide variant	NM_000572.3(IL10):c.334C>T (p.Leu112=)	Inflammatory bowel disease [RCV002543883]\|not provided [RCV001726779]	likely benign	1	206770951	206770951	Human	2	name
151877059	CV1460132	single nucleotide variant	NM_000572.3(IL10):c.37C>A (p.Leu13Met)	Inflammatory bowel disease [RCV002036385]	uncertain significance	1	206772399	206772399	Human	2	name
151763703	CV1478312	single nucleotide variant	NM_000572.3(IL10):c.46G>T (p.Val16Leu)	Inflammatory bowel disease [RCV002008162]	uncertain significance	1	206772390	206772390	Human	2	name
152063469	CV1587810	single nucleotide variant	NM_000572.3(IL10):c.510C>T (p.Ala170=)	Inflammatory bowel disease [RCV002090549]	likely benign	1	206768663	206768663	Human	2	name
156405436	CV1919338	single nucleotide variant	NM_000572.3(IL10):c.62G>A (p.Gly21Asp)	Inflammatory bowel disease [RCV002585646]	uncertain significance	1	206772374	206772374	Human	2	name
156353282	CV1965626	single nucleotide variant	NM_000572.3(IL10):c.327G>A (p.Val109=)	Inflammatory bowel disease [RCV002581211]	likely benign	1	206770958	206770958	Human	2	name
156218467	CV2035599	single nucleotide variant	NM_000572.3(IL10):c.414C>G (p.Ala138=)	Inflammatory bowel disease [RCV002766897]	likely benign	1	206769859	206769859	Human	2	name
156337704	CV2096026	single nucleotide variant	NM_000572.3(IL10):c.372G>A (p.Arg124=)	Inflammatory bowel disease [RCV002900300]	likely benign	1	206770913	206770913	Human	2	name
156128386	CV2158603	single nucleotide variant	NM_000572.3(IL10):c.361C>T (p.Leu121=)	Inflammatory bowel disease [RCV003022078]	likely benign	1	206770924	206770924	Human	2	name
156232833	CV2173142	single nucleotide variant	NM_000572.3(IL10):c.92C>T (p.Thr31Ile)	Inflammatory bowel disease [RCV003059372]	uncertain significance	1	206772344	206772344	Human	2	name
405193112	CV2921112	single nucleotide variant	NM_000572.3(IL10):c.471C>T (p.Ala157=)	Inflammatory bowel disease [RCV003590190]	likely benign	1	206768702	206768702	Human	2	name
407479410	CV3440950	single nucleotide variant	NM_000572.3(IL10):c.34C>G (p.Leu12Val)	not specified [RCV004626380]	uncertain significance	1	206772402	206772402	Human		name
597888312	CV3811885	single nucleotide variant	NM_000572.3(IL10):c.435C>G (p.Ala145=)	Inflammatory bowel disease [RCV005163538]	likely benign	1	206769838	206769838	Human	2	name
597901885	CV3839358	single nucleotide variant	NM_000572.3(IL10):c.492C>T (p.Phe164=)	Inflammatory bowel disease [RCV005176469]	likely benign	1	206768681	206768681	Human	2	name
13500487	CV447726	single nucleotide variant	NM_000572.3(IL10):c.43G>A (p.Gly15Arg)	Inflammatory bowel disease [RCV001257069]\|Susceptibility to HIV infection [RCV003224318]\|not provided [RCV000767995]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	1	206772393	206772393	Human	6	name
13613840	CV515517	single nucleotide variant	NM_000572.3(IL10):c.94C>A (p.His32Asn)	Inflammatory bowel disease [RCV000631401]\|not provided [RCV004791643]	uncertain significance	1	206772342	206772342	Human	2	name
13613838	CV515521	single nucleotide variant	NM_000572.3(IL10):c.58C>T (p.Pro20Ser)	Inflammatory bowel disease [RCV000631402]	uncertain significance	1	206772378	206772378	Human	2	name
15163882	CV732050	single nucleotide variant	NM_000572.3(IL10):c.56G>A (p.Ser19Asn)	Inflammatory bowel disease [RCV000903874]	likely benign	1	206772380	206772380	Human	2	name
15142489	CV746024	single nucleotide variant	NM_000572.3(IL10):c.345C>T (p.Asn115=)	Inflammatory bowel disease [RCV000922027]\|not provided [RCV004711412]	likely benign	1	206770940	206770940	Human	2	name
15200477	CV761491	single nucleotide variant	NM_000572.3(IL10):c.336G>C (p.Leu112=)	Inflammatory bowel disease [RCV000935393]	likely benign	1	206770949	206770949	Human	2	name
15118496	CV780460	single nucleotide variant	NM_000572.3(IL10):c.513C>T (p.Tyr171=)	Inflammatory bowel disease [RCV001446247]	likely benign	1	206768660	206768660	Human	2	name
38479462	CV921817	single nucleotide variant	NM_000572.3(IL10):c.71C>G (p.Thr24Ser)	Inflammatory bowel disease [RCV001217119]	uncertain significance	1	206772365	206772365	Human	2	name
126913949	CV1039745	single nucleotide variant	NM_000572.3(IL10):c.100C>A (p.Pro34Thr)	Inflammatory bowel disease [RCV001359362]\|not provided [RCV004728667]	uncertain significance	1	206772336	206772336	Human	2	name
151745294	CV1401711	single nucleotide variant	NM_000572.3(IL10):c.209T>A (p.Leu70Ter)	Inflammatory bowel disease [RCV001947523]	uncertain significance	1	206771372	206771372	Human	2	name
151757437	CV1459758	single nucleotide variant	NM_000572.3(IL10):c.121C>T (p.Leu41Phe)	Inflammatory bowel disease [RCV001986893]	uncertain significance	1	206772315	206772315	Human	2	name
151803231	CV1462563	single nucleotide variant	NM_000572.3(IL10):c.241C>A (p.Gln81Lys)	Inflammatory bowel disease [RCV002028295]	uncertain significance	1	206771044	206771044	Human	2	name
156273033	CV1899556	single nucleotide variant	NM_000572.3(IL10):c.118A>G (p.Met40Val)	Inflammatory bowel disease [RCV003086853]	uncertain significance	1	206772318	206772318	Human	2	name
156296064	CV2017061	single nucleotide variant	NM_000572.3(IL10):c.112C>G (p.Pro38Ala)	Inflammatory bowel disease [RCV002715848]	uncertain significance	1	206772324	206772324	Human	2	name
156238473	CV2154567	single nucleotide variant	NM_000572.3(IL10):c.137A>G (p.Asp46Gly)	Inflammatory bowel disease [RCV003025916]	uncertain significance	1	206772299	206772299	Human	2	name
155992828	CV2171332	single nucleotide variant	NM_000572.3(IL10):c.257T>A (p.Met86Lys)	Inflammatory bowel disease [RCV003034406]	uncertain significance	1	206771028	206771028	Human	2	name
156277312	CV2287838	single nucleotide variant	NM_000572.3(IL10):c.215A>G (p.Glu72Gly)	not specified [RCV004143279]	uncertain significance	1	206771366	206771366	Human		name
407479551	CV3440951	single nucleotide variant	NM_000572.3(IL10):c.249G>T (p.Leu83Phe)	not specified [RCV004627915]	uncertain significance	1	206771036	206771036	Human		name
597942084	CV3757541	single nucleotide variant	NM_000572.3(IL10):c.146G>A (p.Ser49Asn)	Inflammatory bowel disease [RCV005077727]	uncertain significance	1	206772290	206772290	Human	2	name
26916974	CV823275	single nucleotide variant	NM_000572.3(IL10):c.134G>A (p.Arg45Gln)	Inflammatory bowel disease [RCV001042351]	uncertain significance	1	206772302	206772302	Human	2	name
38458402	CV941669	single nucleotide variant	NM_000572.3(IL10):c.274G>A (p.Glu92Lys)	Inflammatory bowel disease [RCV001228939]	uncertain significance	1	206771011	206771011	Human	2	name
126743548	CV1002437	single nucleotide variant	NM_000572.3(IL10):c.365G>A (p.Arg122Lys)	Inflammatory bowel disease [RCV001325637]	uncertain significance	1	206770920	206770920	Human	2	name
126923247	CV1039744	single nucleotide variant	NM_000572.3(IL10):c.314T>G (p.Ile105Ser)	Inflammatory bowel disease [RCV001365626]	uncertain significance	1	206770971	206770971	Human	2	name
151882552	CV1381787	single nucleotide variant	NM_000572.3(IL10):c.301C>A (p.Gln101Lys)	Inflammatory bowel disease [RCV001941321]	uncertain significance	1	206770984	206770984	Human	2	name
151867084	CV1394123	single nucleotide variant	NM_000572.3(IL10):c.534C>G (p.Asn178Lys)	Inflammatory bowel disease [RCV002035188]	uncertain significance	1	206768639	206768639	Human	2	name
151882102	CV1395996	single nucleotide variant	NM_000572.3(IL10):c.323A>G (p.His108Arg)	Inflammatory bowel disease [RCV002037063]	uncertain significance	1	206770962	206770962	Human	2	name
151764154	CV1403108	single nucleotide variant	NM_000572.3(IL10):c.374G>A (p.Arg125His)	Inflammatory bowel disease [RCV001914327]	uncertain significance	1	206770911	206770911	Human	2	name
151877969	CV1415928	single nucleotide variant	NM_000572.3(IL10):c.502A>G (p.Ile168Val)	Inflammatory bowel disease [RCV001926065]	uncertain significance	1	206768671	206768671	Human	2	name
151802771	CV1437678	single nucleotide variant	NM_000572.3(IL10):c.383G>A (p.Arg128Gln)	Inflammatory bowel disease [RCV001899215]	uncertain significance	1	206769890	206769890	Human	2	name
151768468	CV1445492	single nucleotide variant	NM_000572.3(IL10):c.374G>T (p.Arg125Leu)	Inflammatory bowel disease [RCV002025128]	uncertain significance	1	206770911	206770911	Human	2	name
151850764	CV1450473	single nucleotide variant	NM_000572.3(IL10):c.320C>T (p.Ala107Val)	Inflammatory bowel disease [RCV001922748]	uncertain significance	1	206770965	206770965	Human	2	name
151892492	CV1493519	single nucleotide variant	NM_000572.3(IL10):c.371G>A (p.Arg124Gln)	Inflammatory bowel disease [RCV001944169]	uncertain significance	1	206770914	206770914	Human	2	name
151756402	CV1496938	single nucleotide variant	NM_000572.3(IL10):c.434C>T (p.Ala145Val)	Inflammatory bowel disease [RCV001913489]	uncertain significance	1	206769839	206769839	Human	2	name
151774503	CV1505107	single nucleotide variant	NM_000572.3(IL10):c.521T>C (p.Met174Thr)	Inflammatory bowel disease [RCV001988560]	uncertain significance	1	206768652	206768652	Human	2	name
155720425	CV1775628	single nucleotide variant	NM_000572.3(IL10):c.424G>C (p.Val142Leu)	Inflammatory bowel disease [RCV002301267]	uncertain significance	1	206769849	206769849	Human	2	name
155747014	CV1778155	single nucleotide variant	NM_000572.3(IL10):c.320C>A (p.Ala107Glu)	Inflammatory bowel disease [RCV002303521]	uncertain significance	1	206770965	206770965	Human	2	name
156381812	CV1925153	single nucleotide variant	NM_000572.3(IL10):c.386T>A (p.Phe129Tyr)	Inflammatory bowel disease [RCV002634330]	uncertain significance	1	206769887	206769887	Human	2	name
156270671	CV1970928	single nucleotide variant	NM_000572.3(IL10):c.529C>T (p.Arg177Ter)	Inflammatory bowel disease [RCV002598079]	uncertain significance	1	206768644	206768644	Human	2	name
156371768	CV2007824	single nucleotide variant	NM_000572.3(IL10):c.534C>A (p.Asn178Lys)	Inflammatory bowel disease [RCV002676957]	uncertain significance	1	206768639	206768639	Human	2	name
155999878	CV2057367	single nucleotide variant	NM_000572.3(IL10):c.503T>A (p.Ile168Lys)	Inflammatory bowel disease [RCV002819598]	uncertain significance	1	206768670	206768670	Human	2	name
156332917	CV2061479	single nucleotide variant	NM_000572.3(IL10):c.443A>G (p.Lys148Arg)	Inflammatory bowel disease [RCV002810786]	uncertain significance	1	206769830	206769830	Human	2	name
597847144	CV3768327	single nucleotide variant	NM_000572.3(IL10):c.347T>A (p.Leu116Gln)	Inflammatory bowel disease [RCV005122706]	uncertain significance	1	206770938	206770938	Human	2	name
14735855	CV627319	single nucleotide variant	NM_000572.3(IL10):c.514A>G (p.Met172Val)	Inflammatory bowel disease [RCV000819760]	uncertain significance	1	206768659	206768659	Human	2	name
38488050	CV921816	single nucleotide variant	NM_000572.3(IL10):c.383G>T (p.Arg128Leu)	Inflammatory bowel disease [RCV001221005]	uncertain significance	1	206769890	206769890	Human	2	name
38486200	CV930253	single nucleotide variant	NM_000572.3(IL10):c.507A>C (p.Glu169Asp)	Inflammatory bowel disease [RCV001208795]	uncertain significance	1	206768666	206768666	Human	2	name
38458811	CV952222	single nucleotide variant	NM_000572.3(IL10):c.530G>A (p.Arg177Gln)	Inflammatory bowel disease [RCV001246421]	uncertain significance	1	206768643	206768643	Human	2	name
126762439	CV987175	single nucleotide variant	NM_000572.3(IL10):c.370C>T (p.Arg124Trp)	Inflammatory bowel disease [RCV001309884]\|not specified [RCV004034218]	uncertain significance	1	206770915	206770915	Human	2	name
126725422	CV987176	single nucleotide variant	NM_000572.3(IL10):c.343A>T (p.Asn115Tyr)	Inflammatory bowel disease [RCV001302561]	uncertain significance	1	206770942	206770942	Human	2	name
126764500	CV987177	single nucleotide variant	NM_000572.3(IL10):c.332C>T (p.Ser111Phe)	Inflammatory bowel disease [RCV001301114]	uncertain significance	1	206770953	206770953	Human	2	name
152074151	CV1570429	indel	NM_000572.3(IL10):c.378+19_378+20delinsCC	Inflammatory bowel disease [RCV002210370]	likely benign	1	206770887	206770888	Human		name
28907841	CV867074	single nucleotide variant	NM_001558.4(IL10RA):c.*9G>A	IL10RA-related disorder [RCV003963049]\|Inflammatory bowel disease 28 [RCV001107441]	likely benign\|uncertain significance	11	117999650	117999650	Human	1	name , trait , alternate_id
11613050	CV324452	single nucleotide variant	NM_001558.4(IL10RA):c.-70C>T	Inflammatory bowel disease 28 [RCV000265133]\|not provided [RCV004705205]	likely benign\|uncertain significance	11	117986398	117986398	Human	1	name
11651556	CV324454	single nucleotide variant	NM_001558.4(IL10RA):c.-54T>C	Inflammatory bowel disease 28 [RCV000299480]	uncertain significance	11	117986414	117986414	Human	1	name
11623944	CV336594	single nucleotide variant	NM_000628.5(IL10RB):c.-72C>A	Inflammatory bowel disease 25 [RCV000379182]\|not provided [RCV004703841]	likely benign\|uncertain significance	21	33266394	33266394	Human	1	name
11630207	CV346300	single nucleotide variant	NM_000628.5(IL10RB):c.-74C>A	Inflammatory bowel disease 25 [RCV000343233]	uncertain significance	21	33266392	33266392	Human	1	name
11627479	CV350548	single nucleotide variant	NM_000628.5(IL10RB):c.-94C>A	Inflammatory bowel disease 25 [RCV000283648]	uncertain significance	21	33266372	33266372	Human	1	name
11654097	CV350554	single nucleotide variant	NM_000628.5(IL10RB):c.*17A>G	Inflammatory bowel disease 25 [RCV000314813]	uncertain significance	21	33296374	33296374	Human	1	name
11660717	CV350557	single nucleotide variant	NM_000628.5(IL10RB):c.*20C>T	Inflammatory bowel disease 25 [RCV000369479]	uncertain significance	21	33296377	33296377	Human	1	name
11626811	CV351592	single nucleotide variant	NM_000628.5(IL10RB):c.*85A>G	Inflammatory bowel disease 25 [RCV000270142]\|not provided [RCV004717456]\|not specified [RCV003392210]	benign	21	33296442	33296442	Human	1	name
28909999	CV867068	single nucleotide variant	NM_001558.4(IL10RA):c.-65C>T	Inflammatory bowel disease 28 [RCV001108783]	uncertain significance	11	117986403	117986403	Human	1	name
28910000	CV867069	single nucleotide variant	NM_001558.4(IL10RA):c.-29C>T	Inflammatory bowel disease 28 [RCV001108784]	uncertain significance	11	117986439	117986439	Human	1	name
28902537	CV886687	single nucleotide variant	NM_000628.5(IL10RB):c.-66A>T	Inflammatory bowel disease 25 [RCV001143615]	uncertain significance	21	33266400	33266400	Human	1	name
126744961	CV1030076	single nucleotide variant	NM_001558.4(IL10RA):c.67+6G>T	Inflammatory bowel disease 28 [RCV001351345]	uncertain significance	11	117986540	117986540	Human	1	name
127247288	CV1056636	single nucleotide variant	NM_000628.5(IL10RB):c.49+2T>G	Inflammatory bowel disease 25 [RCV001377748]	likely pathogenic	21	33266516	33266516	Human	1	name
127252717	CV1107360	single nucleotide variant	NM_000628.5(IL10RB):c.49+8G>T	IL10RB-related disorder [RCV003965840]\|Inflammatory bowel disease 25 [RCV001436881]	likely benign	21	33266522	33266522	Human	1	name , trait , alternate_id
151667489	CV1351118	single nucleotide variant	NM_000628.5(IL10RB):c.49+5G>A	Inflammatory bowel disease 25 [RCV001990215]	uncertain significance	21	33266519	33266519	Human	1	name
151727015	CV1488380	single nucleotide variant	NM_001558.4(IL10RA):c.68-1G>A	Inflammatory bowel disease 28 [RCV001966719]	likely pathogenic	11	117988381	117988381	Human	1	name
405175942	CV2948207	single nucleotide variant	NM_001558.4(IL10RA):c.68-6C>T	Inflammatory bowel disease 28 [RCV003639047]	likely benign	11	117988376	117988376	Human	1	name
11611554	CV312453	single nucleotide variant	NM_001558.4(IL10RA):c.*354T>C	Inflammatory bowel disease 28 [RCV000396898]\|not provided [RCV004706796]	benign\|likely benign	11	117999995	117999995	Human	1	name
11609589	CV312454	single nucleotide variant	NM_001558.4(IL10RA):c.*639C>T	Inflammatory bowel disease 28 [RCV000370150]	uncertain significance	11	118000280	118000280	Human	1	name
11600230	CV312455	single nucleotide variant	NM_001558.4(IL10RA):c.*863C>T	Inflammatory bowel disease 28 [RCV000271970]	uncertain significance	11	118000504	118000504	Human	1	name
11605646	CV312459	single nucleotide variant	NM_001558.4(IL10RA):c.*866C>A	Inflammatory bowel disease 28 [RCV000322410]	uncertain significance	11	118000507	118000507	Human	1	name
405274147	CV3195008	single nucleotide variant	NM_001558.4(IL10RA):c.67+8T>G	IL10RA-related disorder [RCV003902249]	likely benign	11	117986542	117986542	Human		name , trait , alternate_id
11648282	CV324484	single nucleotide variant	NM_001558.4(IL10RA):c.*104C>G	Inflammatory bowel disease 28 [RCV000281038]	uncertain significance	11	117999745	117999745	Human	1	name
11621570	CV324491	single nucleotide variant	NM_001558.4(IL10RA):c.*133C>T	Inflammatory bowel disease 28 [RCV000350011]	likely benign\|uncertain significance	11	117999774	117999774	Human	1	name
11654212	CV324506	duplication	NM_001558.4(IL10RA):c.*356dup	Inflammatory bowel disease [RCV000315577]	likely benign	11	117999995	117999996	Human	2	name
11625455	CV324507	single nucleotide variant	NM_001558.4(IL10RA):c.*676C>T	Inflammatory bowel disease 28 [RCV000398873]	uncertain significance	11	118000317	118000317	Human	1	name
11622945	CV324509	single nucleotide variant	NM_001558.4(IL10RA):c.*854C>G	Inflammatory bowel disease 28 [RCV000366437]	uncertain significance	11	118000495	118000495	Human	1	name
11617723	CV325226	single nucleotide variant	NM_001558.4(IL10RA):c.*756T>C	Inflammatory bowel disease 28 [RCV000307178]	likely benign\|uncertain significance	11	118000397	118000397	Human	1	name
11622198	CV325227	single nucleotide variant	NM_001558.4(IL10RA):c.*968G>A	Inflammatory bowel disease 28 [RCV000357651]	benign\|uncertain significance	11	118000609	118000609	Human	1	name
11623752	CV336602	single nucleotide variant	NM_000628.5(IL10RB):c.*515C>T	Inflammatory bowel disease 25 [RCV000376575]	uncertain significance	21	33296872	33296872	Human	1	name
11657012	CV336606	single nucleotide variant	NM_000628.5(IL10RB):c.*616A>G	Inflammatory bowel disease 25 [RCV000338187]	uncertain significance	21	33296973	33296973	Human	1	name
11658405	CV336608	single nucleotide variant	NM_000628.5(IL10RB):c.*796T>C	Inflammatory bowel disease 25 [RCV000348570]	uncertain significance	21	33297153	33297153	Human	1	name
11645847	CV346309	single nucleotide variant	NM_000628.5(IL10RB):c.*546G>A	Inflammatory bowel disease 25 [RCV000267491]	uncertain significance	21	33296903	33296903	Human	1	name
11631340	CV346315	single nucleotide variant	NM_000628.5(IL10RB):c.*719G>A	Inflammatory bowel disease 25 [RCV000374106]\|not provided [RCV004717458]	benign	21	33297076	33297076	Human	1	name
11631928	CV346316	single nucleotide variant	NM_000628.5(IL10RB):c.*816T>C	Inflammatory bowel disease 25 [RCV000391576]	uncertain significance	21	33297173	33297173	Human	1	name
11654978	CV350559	single nucleotide variant	NM_000628.5(IL10RB):c.*365C>T	Inflammatory bowel disease [RCV000322001]	uncertain significance	21	33296722	33296722	Human	2	name
11628688	CV351595	single nucleotide variant	NM_000628.5(IL10RB):c.*135G>A	Inflammatory bowel disease 25 [RCV000306565]\|not provided [RCV004717457]	benign\|likely benign	21	33296492	33296492	Human	1	name
11631012	CV351596	single nucleotide variant	NM_000628.5(IL10RB):c.*314G>A	Inflammatory bowel disease 25 [RCV000366107]\|not provided [RCV004718538]	benign	21	33296671	33296671	Human	1	name
11626890	CV351598	single nucleotide variant	NM_000628.5(IL10RB):c.*334G>A	Inflammatory bowel disease 25 [RCV000271439]	benign\|likely benign	21	33296691	33296691	Human	1	name
11661037	CV351601	deletion	NM_000628.5(IL10RB):c.*616del	Inflammatory bowel disease [RCV000372654]\|not provided [RCV004694631]	uncertain significance	21	33296954	33296954	Human	2	name
11628118	CV351603	single nucleotide variant	NM_000628.5(IL10RB):c.*761C>T	Inflammatory bowel disease 25 [RCV000293621]	uncertain significance	21	33297118	33297118	Human	1	name
598197995	CV3892484	single nucleotide variant	NM_000628.5(IL10RB):c.50-2A>T	not provided [RCV005254317]	pathogenic	21	33268392	33268392	Human		name
13490884	CV460898	single nucleotide variant	NM_001558.4(IL10RA):c.67+8T>C	Inflammatory bowel disease 28 [RCV000556310]\|not provided [RCV001091034]	benign\|likely benign\|conflicting interpretations of pathogenicity	11	117986542	117986542	Human	1	name
13618309	CV533819	single nucleotide variant	NM_000628.5(IL10RB):c.50-4A>G	Inflammatory bowel disease 25 [RCV000645976]	likely benign	21	33268390	33268390	Human	1	name
28907842	CV867075	single nucleotide variant	NM_001558.4(IL10RA):c.*203G>T	Inflammatory bowel disease 28 [RCV001107442]	uncertain significance	11	117999844	117999844	Human	1	name
28907846	CV867076	single nucleotide variant	NM_001558.4(IL10RA):c.*328G>C	Inflammatory bowel disease 28 [RCV001107443]	uncertain significance	11	117999969	117999969	Human	1	name
28900401	CV867077	single nucleotide variant	NM_001558.4(IL10RA):c.*405G>A	Inflammatory bowel disease 28 [RCV001103817]	uncertain significance	11	118000046	118000046	Human	1	name
28900404	CV867078	single nucleotide variant	NM_001558.4(IL10RA):c.*421A>C	Inflammatory bowel disease 28 [RCV001103818]	uncertain significance	11	118000062	118000062	Human	1	name
28900407	CV867079	single nucleotide variant	NM_001558.4(IL10RA):c.*543G>A	Inflammatory bowel disease 28 [RCV001103819]	uncertain significance	11	118000184	118000184	Human	1	name
28900411	CV867080	single nucleotide variant	NM_001558.4(IL10RA):c.*576G>C	Inflammatory bowel disease 28 [RCV001103820]	uncertain significance	11	118000217	118000217	Human	1	name
28904860	CV867081	single nucleotide variant	NM_001558.4(IL10RA):c.*846T>A	Inflammatory bowel disease 28 [RCV001105766]	uncertain significance	11	118000487	118000487	Human	1	name
28904864	CV867082	single nucleotide variant	NM_001558.4(IL10RA):c.*872G>A	Inflammatory bowel disease 28 [RCV001105767]	uncertain significance	11	118000513	118000513	Human	1	name
28904868	CV867083	single nucleotide variant	NM_001558.4(IL10RA):c.*984C>A	Inflammatory bowel disease 28 [RCV001105768]	likely benign	11	118000625	118000625	Human	1	name
28898277	CV886688	single nucleotide variant	NM_000628.5(IL10RB):c.*519A>G	Inflammatory bowel disease 25 [RCV001141911]	uncertain significance	21	33296876	33296876	Human	1	name
28898280	CV886689	single nucleotide variant	NM_000628.5(IL10RB):c.*536G>T	Inflammatory bowel disease 25 [RCV001141912]	uncertain significance	21	33296893	33296893	Human	1	name
126742665	CV1018734	single nucleotide variant	NM_000628.5(IL10RB):c.331+1G>C	Inflammatory bowel disease 25 [RCV001330007]	likely pathogenic	21	33276754	33276754	Human	1	name
127245882	CV1056637	single nucleotide variant	NM_000628.5(IL10RB):c.173+2T>G	Inflammatory bowel disease 25 [RCV001377497]	pathogenic\|likely pathogenic	21	33268519	33268519	Human	1	name
151820739	CV1378453	single nucleotide variant	NM_001558.4(IL10RA):c.367+4C>T	Inflammatory bowel disease 28 [RCV002029869]	uncertain significance	11	117989624	117989624	Human	1	name
151864981	CV1405923	single nucleotide variant	NM_001558.4(IL10RA):c.810+6T>A	Inflammatory bowel disease 28 [RCV001959715]	uncertain significance	11	117995716	117995716	Human	1	name
152027764	CV1529568	single nucleotide variant	NM_000628.5(IL10RB):c.49+19G>T	Inflammatory bowel disease 25 [RCV002185611]	likely benign	21	33266533	33266533	Human	1	name
152132984	CV1557378	single nucleotide variant	NM_001558.4(IL10RA):c.68-16A>G	Inflammatory bowel disease 28 [RCV002137175]	benign	11	117988366	117988366	Human	1	name
152106117	CV1605105	single nucleotide variant	NM_001558.4(IL10RA):c.67+20C>T	Inflammatory bowel disease 28 [RCV002196169]	likely benign	11	117986554	117986554	Human	1	name
152130056	CV1607918	deletion	NM_000628.5(IL10RB):c.332-5del	Inflammatory bowel disease 25 [RCV002176679]	likely benign	21	33279747	33279747	Human	1	name
152134439	CV1645960	single nucleotide variant	NM_001558.4(IL10RA):c.67+17C>T	Inflammatory bowel disease 28 [RCV002177235]	likely benign	11	117986551	117986551	Human	1	name
152028185	CV1655115	deletion	NM_000628.5(IL10RB):c.647-7del	Inflammatory bowel disease 25 [RCV002105148]	benign	21	33288094	33288094	Human	1	name
152140540	CV1660876	single nucleotide variant	NM_000628.5(IL10RB):c.49+12G>A	Inflammatory bowel disease 25 [RCV002120305]	likely benign	21	33266526	33266526	Human	1	name
156350059	CV1886052	single nucleotide variant	NM_000628.5(IL10RB):c.50-20T>C	Inflammatory bowel disease 25 [RCV003090902]	likely benign	21	33268374	33268374	Human	1	name
156101504	CV1960331	single nucleotide variant	NM_001558.4(IL10RA):c.689-8G>T	Inflammatory bowel disease 28 [RCV002570864]	likely benign	11	117995581	117995581	Human	1	name
156385440	CV1990092	single nucleotide variant	NM_000628.5(IL10RB):c.49+19G>A	Inflammatory bowel disease 25 [RCV002634581]	likely benign	21	33266533	33266533	Human	1	name
156212219	CV2036977	single nucleotide variant	NM_000628.5(IL10RB):c.50-15G>A	Inflammatory bowel disease 25 [RCV002790287]	likely benign	21	33268379	33268379	Human	1	name
156238448	CV2154559	single nucleotide variant	NM_000628.5(IL10RB):c.331+4A>T	Inflammatory bowel disease 25 [RCV003025915]	uncertain significance	21	33276757	33276757	Human	1	name
156015820	CV2177468	deletion	NM_000628.5(IL10RB):c.332-7del	Inflammatory bowel disease 25 [RCV003035478]	likely benign	21	33279745	33279745	Human	1	name
11636494	CV273890	single nucleotide variant	NM_001558.4(IL10RA):c.67+10C>T	Inflammatory bowel disease 28 [RCV001470596]\|not provided [RCV000268478]	likely benign\|uncertain significance	11	117986544	117986544	Human	1	name
401930845	CV2795617	single nucleotide variant	NM_000628.5(IL10RB):c.49+40G>A	not specified [RCV003391179]	benign	21	33266554	33266554	Human		name
401906887	CV2795740	single nucleotide variant	NM_001558.4(IL10RA):c.67+89G>C	not specified [RCV003397092]	benign	11	117986623	117986623	Human		name
404994982	CV2865181	single nucleotide variant	NM_000628.5(IL10RB):c.174-1G>A	Inflammatory bowel disease 25 [RCV003525550]	likely pathogenic	21	33276595	33276595	Human	1	name
405180321	CV2957356	single nucleotide variant	NM_001558.4(IL10RA):c.689-8G>A	Inflammatory bowel disease 28 [RCV003639477]	likely benign	11	117995581	117995581	Human	1	name
11662662	CV312436	single nucleotide variant	NM_001558.4(IL10RA):c.67+15C>T	Inflammatory bowel disease 28 [RCV000387985]	conflicting interpretations of pathogenicity\|uncertain significance	11	117986549	117986549	Human	1	name
11645868	CV312460	single nucleotide variant	NM_001558.4(IL10RA):c.*1058A>G	Inflammatory bowel disease 28 [RCV000267574]	uncertain significance	11	118000699	118000699	Human	1	name
11605694	CV312461	single nucleotide variant	NM_001558.4(IL10RA):c.*1348G>C	Inflammatory bowel disease 28 [RCV000322630]\|not provided [RCV004706797]	benign\|likely benign	11	118000989	118000989	Human	1	name
11600925	CV312465	single nucleotide variant	NM_001558.4(IL10RA):c.*1375C>A	Inflammatory bowel disease 28 [RCV000278255]	uncertain significance	11	118001016	118001016	Human	1	name
11609790	CV318360	single nucleotide variant	NM_001558.4(IL10RA):c.*1352G>A	Inflammatory bowel disease 28 [RCV000372581]	likely benign\|uncertain significance	11	118000993	118000993	Human	1	name
11602903	CV318366	single nucleotide variant	NM_001558.4(IL10RA):c.*1730G>A	Inflammatory bowel disease 28 [RCV000294858]\|not provided [RCV004706798]	benign	11	118001371	118001371	Human	1	name
11612422	CV324456	single nucleotide variant	NM_001558.4(IL10RA):c.67+11G>A	Inflammatory bowel disease 28 [RCV000259364]	conflicting interpretations of pathogenicity\|uncertain significance	11	117986545	117986545	Human	1	name
11654377	CV324465	single nucleotide variant	NM_001558.4(IL10RA):c.67+13G>A	Inflammatory bowel disease 28 [RCV000316968]	conflicting interpretations of pathogenicity\|uncertain significance	11	117986547	117986547	Human	1	name
11618913	CV324511	single nucleotide variant	NM_001558.4(IL10RA):c.*1412T>C	Inflammatory bowel disease 28 [RCV000319341]	benign\|likely benign	11	118001053	118001053	Human	1	name
11623528	CV324512	single nucleotide variant	NM_001558.4(IL10RA):c.*1555C>T	Inflammatory bowel disease 28 [RCV000373883]	uncertain significance	11	118001196	118001196	Human	1	name
11650577	CV324516	single nucleotide variant	NM_001558.4(IL10RA):c.*1664A>G	Inflammatory bowel disease 28 [RCV000293550]	uncertain significance	11	118001305	118001305	Human	1	name
11664413	CV324517	single nucleotide variant	NM_001558.4(IL10RA):c.*1722T>C	Inflammatory bowel disease 28 [RCV000405254]	uncertain significance	11	118001363	118001363	Human	1	name
11615992	CV325209	single nucleotide variant	NM_001558.4(IL10RA):c.188+3G>A	Inflammatory bowel disease 28 [RCV000290374]	uncertain significance	11	117988505	117988505	Human	1	name
11621420	CV325241	single nucleotide variant	NM_001558.4(IL10RA):c.*1684G>A	Inflammatory bowel disease 28 [RCV000348592]	uncertain significance	11	118001325	118001325	Human	1	name
407475828	CV3415689	deletion	NM_000628.5(IL10RB):c.804+2del	Susceptibility to severe COVID-19 [RCV004598566]	likely pathogenic	21	33288263	33288263	Human		name
597692972	CV3717282	single nucleotide variant	NM_000628.5(IL10RB):c.805-2A>C	Hepatitis B virus, susceptibility to [RCV005032697]	likely pathogenic	21	33296182	33296182	Human	1	name
597954195	CV3757161	single nucleotide variant	NM_000628.5(IL10RB):c.332-4T>A	Inflammatory bowel disease 25 [RCV005080022]	likely benign	21	33279748	33279748	Human	1	name
597936644	CV3759526	single nucleotide variant	NM_001558.4(IL10RA):c.538-9T>C	Inflammatory bowel disease 28 [RCV005076646]	likely benign	11	117993990	117993990	Human	1	name
597973277	CV3801040	duplication	NM_000628.5(IL10RB):c.332-3dup	Inflammatory bowel disease 25 [RCV005143235]	likely benign	21	33279747	33279748	Human	1	name
597878887	CV3826170	single nucleotide variant	NM_001558.4(IL10RA):c.537+9T>C	Inflammatory bowel disease 28 [RCV005177866]	likely benign	11	117993419	117993419	Human	1	name
597967193	CV3855748	single nucleotide variant	NM_000628.5(IL10RB):c.646+8C>G	Inflammatory bowel disease 25 [RCV005194728]	likely benign	21	33283249	33283249	Human	1	name
597921670	CV3861803	single nucleotide variant	NM_000628.5(IL10RB):c.331+1G>A	Inflammatory bowel disease 25 [RCV005205179]	likely pathogenic	21	33276754	33276754	Human	1	name
13484176	CV461229	single nucleotide variant	NM_001558.4(IL10RA):c.811-9C>T	Inflammatory bowel disease 28 [RCV000552643]	likely benign	11	117998706	117998706	Human	1	name
26893779	CV852397	single nucleotide variant	NM_000628.5(IL10RB):c.647-3C>T	Inflammatory bowel disease 25 [RCV001069140]	uncertain significance	21	33288101	33288101	Human	1	name
28906842	CV867084	single nucleotide variant	NM_001558.4(IL10RA):c.*1147C>T	Inflammatory bowel disease 28 [RCV001106881]	uncertain significance	11	118000788	118000788	Human	1	name
28900035	CV868605	single nucleotide variant	NM_001558.4(IL10RA):c.67+11G>C	Inflammatory bowel disease 28 [RCV001103630]	conflicting interpretations of pathogenicity\|uncertain significance	11	117986545	117986545	Human	1	name
41406584	CV980489	single nucleotide variant	NM_000628.5(IL10RB):c.804+8G>A	Hepatitis B virus, susceptibility to [RCV003224552]\|IL10RB-related disorder [RCV003953626]\|Inflammatory bowel disease 25 [RCV002069497]	likely benign\|uncertain significance	21	33288269	33288269	Human	2	name , trait , alternate_id
126753193	CV1035901	deletion	NM_001558.4(IL10RA):c.1_67+1del	Inflammatory bowel disease 28 [RCV001352890]	pathogenic	11	117986466	117986533	Human	1	name
127251805	CV1077888	deletion	NM_001558.4(IL10RA):c.367+10del	Inflammatory bowel disease 28 [RCV001400203]	likely benign	11	117989629	117989629	Human	1	name
127304494	CV1121084	single nucleotide variant	NM_001558.4(IL10RA):c.538-10T>G	Inflammatory bowel disease 28 [RCV001454977]	likely benign	11	117993989	117993989	Human	1	name
127307360	CV1156577	single nucleotide variant	NM_001558.4(IL10RA):c.368-18C>A	Inflammatory bowel disease 28 [RCV001517067]\|not provided [RCV004707641]	benign	11	117993223	117993223	Human	1	name
127320298	CV1156578	single nucleotide variant	NM_001558.4(IL10RA):c.368-18C>G	Inflammatory bowel disease 28 [RCV001522573]\|not provided [RCV003399320]	benign\|likely benign	11	117993223	117993223	Human	1	name
127308775	CV1158969	single nucleotide variant	NM_000628.5(IL10RB):c.173+19T>C	Inflammatory bowel disease 25 [RCV001517635]	benign	21	33268536	33268536	Human	1	name
127316593	CV1158970	single nucleotide variant	NM_000628.5(IL10RB):c.646+19C>A	Hepatitis B virus, susceptibility to [RCV002501831]\|Inflammatory bowel disease 25 [RCV001520567]	benign\|likely benign	21	33283260	33283260	Human	2	name
151815754	CV1486087	single nucleotide variant	NM_001558.4(IL10RA):c.810+11C>T	Inflammatory bowel disease 28 [RCV002049292]	likely benign\|uncertain significance	11	117995721	117995721	Human	1	name
152168196	CV1524790	single nucleotide variant	NM_000628.5(IL10RB):c.332-11C>G	Inflammatory bowel disease 25 [RCV002182359]	likely benign	21	33279741	33279741	Human	1	name
152133274	CV1547106	single nucleotide variant	NM_001558.4(IL10RA):c.811-13C>T	Inflammatory bowel disease 28 [RCV002155818]	likely benign	11	117998702	117998702	Human	1	name
152120478	CV1547267	single nucleotide variant	NM_001558.4(IL10RA):c.368-16C>A	Inflammatory bowel disease 28 [RCV002154190]	likely benign	11	117993225	117993225	Human	1	name
152091988	CV1567704	single nucleotide variant	NM_000628.5(IL10RB):c.174-18A>G	Inflammatory bowel disease 25 [RCV002212853]	likely benign	21	33276578	33276578	Human	1	name
152126796	CV1571983	single nucleotide variant	NM_001558.4(IL10RA):c.537+17G>T	Inflammatory bowel disease 28 [RCV002217521]	likely benign	11	117993427	117993427	Human	1	name
152071492	CV1591608	single nucleotide variant	NM_000628.5(IL10RB):c.174-14T>C	Inflammatory bowel disease 25 [RCV002210038]	likely benign	21	33276582	33276582	Human	1	name
152096927	CV1599826	single nucleotide variant	NM_001558.4(IL10RA):c.368-20C>T	Inflammatory bowel disease 28 [RCV002151317]	likely benign	11	117993221	117993221	Human	1	name
152097599	CV1599974	single nucleotide variant	NM_000628.5(IL10RB):c.647-16C>G	Inflammatory bowel disease 25 [RCV002151397]	likely benign	21	33288088	33288088	Human	1	name
152136213	CV1634578	single nucleotide variant	NM_000628.5(IL10RB):c.804+17G>A	Inflammatory bowel disease 25 [RCV002218751]	likely benign	21	33288278	33288278	Human	1	name
152040151	CV1644083	single nucleotide variant	NM_001558.4(IL10RA):c.368-20C>A	Inflammatory bowel disease 28 [RCV002125970]	likely benign	11	117993221	117993221	Human	1	name
152099840	CV1664024	single nucleotide variant	NM_001558.4(IL10RA):c.688+17G>A	Inflammatory bowel disease 28 [RCV002078843]	likely benign	11	117994166	117994166	Human	1	name
156270234	CV1899361	single nucleotide variant	NM_001558.4(IL10RA):c.811-11C>G	Inflammatory bowel disease 28 [RCV003086754]	likely benign	11	117998704	117998704	Human	1	name
156417936	CV1920751	single nucleotide variant	NM_001558.4(IL10RA):c.368-18C>T	Inflammatory bowel disease 28 [RCV002611105]	likely benign	11	117993223	117993223	Human	1	name
156419404	CV1932779	single nucleotide variant	NM_001558.4(IL10RA):c.188+18G>A	Inflammatory bowel disease 28 [RCV002612636]	likely benign	11	117988520	117988520	Human	1	name
156292601	CV1958589	single nucleotide variant	NM_000628.5(IL10RB):c.804+13G>A	Inflammatory bowel disease 25 [RCV002577891]	likely benign	21	33288274	33288274	Human	1	name
156057688	CV1974649	single nucleotide variant	NM_001558.4(IL10RA):c.367+12C>G	Inflammatory bowel disease 28 [RCV002590868]	likely benign	11	117989632	117989632	Human	1	name
155943418	CV2064580	single nucleotide variant	NM_001558.4(IL10RA):c.367+10C>T	Inflammatory bowel disease 28 [RCV002839560]	likely benign	11	117989630	117989630	Human	1	name
156012188	CV2071866	single nucleotide variant	NM_000628.5(IL10RB):c.646+14T>C	Inflammatory bowel disease 25 [RCV002843933]	likely benign	21	33283255	33283255	Human	1	name
155917909	CV2073547	single nucleotide variant	NM_001558.4(IL10RA):c.189-12G>C	Inflammatory bowel disease 28 [RCV002838159]	likely benign	11	117989430	117989430	Human	1	name
155967655	CV2152284	single nucleotide variant	NM_001558.4(IL10RA):c.811-15C>T	Inflammatory bowel disease 28 [RCV003015782]	likely benign	11	117998700	117998700	Human	1	name
156065404	CV2170689	single nucleotide variant	NM_000628.5(IL10RB):c.646+19C>T	Inflammatory bowel disease 25 [RCV003019872]	likely benign	21	33283260	33283260	Human	1	name
156336910	CV2178230	single nucleotide variant	NM_001558.4(IL10RA):c.188+14A>G	Inflammatory bowel disease 28 [RCV003047527]	likely benign	11	117988516	117988516	Human	1	name
401906976	CV2795704	single nucleotide variant	NM_000628.5(IL10RB):c.331+65G>A	not specified [RCV003397056]	benign	21	33276818	33276818	Human		name
401934068	CV2809888	single nucleotide variant	NM_001558.4(IL10RA):c.67+139C>T	not provided [RCV003410927]	likely benign	11	117986673	117986673	Human		name
404987926	CV2849510	single nucleotide variant	NM_001558.4(IL10RA):c.68-114G>A	not specified [RCV003490367]	benign	11	117988268	117988268	Human		name
405012467	CV2903146	deletion	NM_000628.5(IL10RB):c.332-17del	Inflammatory bowel disease 25 [RCV003527394]	likely benign	21	33279735	33279735	Human	1	name
405183490	CV2979966	single nucleotide variant	NM_001558.4(IL10RA):c.689-14C>T	Inflammatory bowel disease 28 [RCV003639932]	likely benign	11	117995575	117995575	Human	1	name
405182660	CV2985571	single nucleotide variant	NM_000628.5(IL10RB):c.804+12G>A	Inflammatory bowel disease 25 [RCV003639849]	likely benign	21	33288273	33288273	Human	1	name
405176051	CV3061664	single nucleotide variant	NM_001558.4(IL10RA):c.538-20T>C	Inflammatory bowel disease 28 [RCV003639095]	likely benign	11	117993979	117993979	Human	1	name
405175711	CV3068636	single nucleotide variant	NM_000628.5(IL10RB):c.498+19A>G	Inflammatory bowel disease 25 [RCV003639084]	likely benign	21	33279937	33279937	Human	1	name
405178959	CV3077099	single nucleotide variant	NM_001558.4(IL10RA):c.537+20C>G	Inflammatory bowel disease 28 [RCV003639307]	likely benign	11	117993430	117993430	Human	1	name
405179386	CV3077895	single nucleotide variant	NM_001558.4(IL10RA):c.537+18G>T	Inflammatory bowel disease 28 [RCV003639365]	likely benign	11	117993428	117993428	Human	1	name
405179016	CV3080508	single nucleotide variant	NM_001558.4(IL10RA):c.368-20C>G	Inflammatory bowel disease 28 [RCV003639328]	likely benign	11	117993221	117993221	Human	1	name
405001914	CV3120587	single nucleotide variant	NM_001558.4(IL10RA):c.537+12C>T	Inflammatory bowel disease 28 [RCV003828189]	likely benign	11	117993422	117993422	Human	1	name
405241076	CV3176796	single nucleotide variant	NM_001558.4(IL10RA):c.537+13C>G	Inflammatory bowel disease 28 [RCV003867234]	likely benign	11	117993423	117993423	Human	1	name
405253751	CV3178585	single nucleotide variant	NM_000628.5(IL10RB):c.647-17C>T	Inflammatory bowel disease 25 [RCV003871186]	likely benign	21	33288087	33288087	Human	1	name
11599865	CV318356	single nucleotide variant	NM_001558.4(IL10RA):c.810+10G>A	Inflammatory bowel disease 28 [RCV000967931]	benign\|likely benign\|uncertain significance	11	117995720	117995720	Human	1	name
11628351	CV351591	single nucleotide variant	NM_000628.5(IL10RB):c.174-14T>G	Inflammatory bowel disease 25 [RCV000299840]	conflicting interpretations of pathogenicity\|uncertain significance	21	33276582	33276582	Human	1	name
11655045	CV351599	microsatellite	NM_000628.5(IL10RB):c.*593TC[1]	Inflammatory bowel disease [RCV000322612]	uncertain significance	21	33296950	33296951	Human		name
597831623	CV3750922	single nucleotide variant	NM_001558.4(IL10RA):c.367+12C>T	Inflammatory bowel disease 28 [RCV005084666]	likely benign	11	117989632	117989632	Human	1	name
597954975	CV3754099	single nucleotide variant	NM_001558.4(IL10RA):c.538-14C>A	Inflammatory bowel disease 28 [RCV005080142]	likely benign	11	117993985	117993985	Human	1	name
597922400	CV3775692	single nucleotide variant	NM_001558.4(IL10RA):c.538-11T>A	Inflammatory bowel disease 28 [RCV005115407]	likely benign	11	117993988	117993988	Human	1	name
597913885	CV3778772	single nucleotide variant	NM_000628.5(IL10RB):c.332-17C>T	Inflammatory bowel disease 25 [RCV005129117]	likely benign	21	33279735	33279735	Human	1	name
597831077	CV3820208	single nucleotide variant	NM_000628.5(IL10RB):c.499-14G>T	Inflammatory bowel disease 25 [RCV005169985]	likely benign	21	33283080	33283080	Human	1	name
597967280	CV3824196	single nucleotide variant	NM_001558.4(IL10RA):c.188+11G>A	Inflammatory bowel disease 28 [RCV005165419]	likely benign	11	117988513	117988513	Human	1	name
597972185	CV3829504	single nucleotide variant	NM_001558.4(IL10RA):c.537+16A>G	Inflammatory bowel disease 28 [RCV005167291]	likely benign	11	117993426	117993426	Human	1	name
597952387	CV3843762	single nucleotide variant	NM_000628.5(IL10RB):c.173+14C>T	Inflammatory bowel disease 25 [RCV005190624]	likely benign	21	33268531	33268531	Human	1	name
597967848	CV3853280	single nucleotide variant	NM_001558.4(IL10RA):c.689-18A>T	Inflammatory bowel disease 28 [RCV005194922]	likely benign	11	117995571	117995571	Human	1	name
28883844	CV887502	single nucleotide variant	NM_000628.5(IL10RB):c.332-11C>T	Inflammatory bowel disease 25 [RCV001137042]	conflicting interpretations of pathogenicity\|uncertain significance	21	33279741	33279741	Human	1	name
38461757	CV920421	single nucleotide variant	NM_000628.5(IL10RB):c.647-14A>C	Inflammatory bowel disease 25 [RCV001197905]	conflicting interpretations of pathogenicity\|uncertain significance	21	33288090	33288090	Human	1	name
8586785	CV121407	single nucleotide variant	NM_000628.4(IL10RB):c.498+405G>A	Lung cancer [RCV000101927]	uncertain significance	21	33280323	33280323	Human		name
401906780	CV2795692	single nucleotide variant	NM_000628.5(IL10RB):c.805-2113A>G	not specified [RCV003397044]	benign	21	33294071	33294071	Human		name
401906893	CV2795709	single nucleotide variant	NM_000628.5(IL10RB):c.805-2099G>A	not specified [RCV003397061]	benign	21	33294085	33294085	Human		name
11627248	CV350560	deletion	NM_000628.5(IL10RB):c.615_616del	Inflammatory bowel disease [RCV000278486]	benign	21	33296954	33296955	Human	2	name
402477239	CV2849439	single nucleotide variant	NM_001405849.1(IL10RB):c.805-886C>A	not specified [RCV003490296]	benign	21	33308090	33308090	Human		name
402477257	CV2849531	single nucleotide variant	NM_001405849.1(IL10RB):c.805-591T>G	not specified [RCV003490388]	benign	21	33308385	33308385	Human		name
152144659	CV1576499	duplication	NM_001558.4(IL10RA):c.537+7_537+10dup	Inflammatory bowel disease 28 [RCV002101277]	likely benign	11	117993416	117993417	Human	1	name
404997488	CV2867874	deletion	NM_001558.4(IL10RA):c.810+19_810+24del	Inflammatory bowel disease 28 [RCV003525772]	likely benign	11	117995728	117995733	Human	1	name
13509407	CV480624	single nucleotide variant	NM_000660.7(TGFB1):c.133C>T (p.Arg45Cys)	Encephalopathy [RCV000584758]\|Inflammatory bowel disease, immunodeficiency, and encephalopathy [RCV000723358]	pathogenic\|likely pathogenic	19	41352912	41352912	Human	3	alternate_id
13509404	CV481174	single nucleotide variant	NM_000660.7(TGFB1):c.328C>T (p.Arg110Cys)	Encephalopathy [RCV000584755]\|Inflammatory bowel disease, immunodeficiency, and encephalopathy [RCV000723357]	pathogenic\|likely pathogenic	19	41352717	41352717	Human	3	alternate_id
13509406	CV481175	single nucleotide variant	NM_000660.7(TGFB1):c.1159T>C (p.Cys387Arg)	Encephalopathy [RCV000584756]\|Inflammatory bowel disease, immunodeficiency, and encephalopathy [RCV000723356]	pathogenic\|likely pathogenic	19	41331066	41331066	Human	3	alternate_id
14352085	CV589848	single nucleotide variant	NM_001354930.2(RIPK1):c.1278C>A (p.Tyr426Ter)	IL10-related early-onset inflammatory bowel disease [RCV000754604]	pathogenic	6	3105753	3105753	Human	1	trait
14352089	CV589849	single nucleotide variant	NM_001354930.2(RIPK1):c.1802G>A (p.Cys601Tyr)	IL10-related early-onset inflammatory bowel disease [RCV000754606]	pathogenic	6	3113125	3113125	Human	1	trait
14352081	CV589850	single nucleotide variant	NM_001354930.2(RIPK1):c.1844T>C (p.Ile615Thr)	IL10-related early-onset inflammatory bowel disease [RCV000754602]	pathogenic	6	3113167	3113167	Human	1	trait
14352088	CV589847	deletion	NM_001354930.2(RIPK1):c.954del (p.Met318fs)	IL10-related early-onset inflammatory bowel disease [RCV000754605]\|Immunodeficiency 57 [RCV000985125]	pathogenic\|likely pathogenic	6	3104263	3104263	Human	1	trait
14352083	CV589851	single nucleotide variant	NM_001354930.2(RIPK1):c.1934C>T (p.Thr645Met)	Autoinflammation with episodic fever and lymphadenopathy [RCV003989593]\|IL10-related early-onset inflammatory bowel disease [RCV000754603]\|Immunodeficiency 57 [RCV001331110]\|See cases [RCV003324714]\|not provided [RCV001855836]	pathogenic\|likely pathogenic\|uncertain significance	6	3113257	3113257	Human	2	trait
11612258	CV312443	single nucleotide variant	NM_001558.4(IL10RA):c.1452G>A (p.Glu484=)	IL10RA-related disorder [RCV003950015]\|Inflammatory bowel disease 28 [RCV000406462]\|not provided [RCV001311792]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	11	117999356	117999356	Human	1	name , trait , alternate_id
11607286	CV318325	single nucleotide variant	NM_001558.4(IL10RA):c.337G>A (p.Val113Ile)	IL10RA-related disorder [RCV003983003]\|Inflammatory bowel disease 28 [RCV000539178]\|not provided [RCV003409467]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	11	117989590	117989590	Human	1	name , trait , alternate_id
405291766	CV3206119	single nucleotide variant	NM_000628.5(IL10RB):c.588T>C (p.Pro196=)	IL10RB-related disorder [RCV003964190]\|Inflammatory bowel disease 25 [RCV005064890]	likely benign	21	33283183	33283183	Human	1	name , trait , alternate_id
11619350	CV325216	single nucleotide variant	NM_001558.4(IL10RA):c.1188G>A (p.Arg396=)	IL10RA-related disorder [RCV003920241]\|Inflammatory bowel disease 28 [RCV000971021]	benign\|likely benign\|uncertain significance	11	117999092	117999092	Human	1	name , trait , alternate_id
11627355	CV346301	single nucleotide variant	NM_000628.5(IL10RB):c.73G>A (p.Glu25Lys)	IL10RB-related disorder [RCV003910322]\|Inflammatory bowel disease 25 [RCV000544667]\|not provided [RCV004703842]	benign\|likely benign\|uncertain significance	21	33268417	33268417	Human	1	name , trait , alternate_id
11629882	CV350553	single nucleotide variant	NM_000628.5(IL10RB):c.131C>T (p.Ala44Val)	IL10RB-related disorder [RCV003950177]\|Inflammatory bowel disease 25 [RCV000335085]	benign\|likely benign\|uncertain significance	21	33268475	33268475	Human	1	name , trait , alternate_id
13476118	CV460933	single nucleotide variant	NM_001558.4(IL10RA):c.312C>T (p.Asp104=)	IL10RA-related disorder [RCV003979999]\|Inflammatory bowel disease 28 [RCV000526589]\|not provided [RCV004707331]	benign	11	117989565	117989565	Human	1	name , trait , alternate_id
8570418	CV48031	single nucleotide variant	NM_001558.4(IL10RA):c.301C>T (p.Arg101Trp)	IL10RA-related disorder [RCV003398584]\|Inflammatory bowel disease 28 [RCV000032627]	pathogenic\|likely pathogenic	11	117989554	117989554	Human	1	name , trait , alternate_id
13619999	CV526008	single nucleotide variant	NM_001558.4(IL10RA):c.1518G>A (p.Leu506=)	IL10RA-related disorder [RCV003965373]\|Inflammatory bowel disease 28 [RCV001463531]	likely benign	11	117999422	117999422	Human	1	name , trait , alternate_id
13618300	CV533835	single nucleotide variant	NM_000628.5(IL10RB):c.442G>A (p.Val148Met)	IL10RB-related disorder [RCV003953159]\|Inflammatory bowel disease 25 [RCV001083772]\|not provided [RCV000762358]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	21	33279862	33279862	Human	1	name , trait , alternate_id
13812854	CV564442	single nucleotide variant	NM_001558.4(IL10RA):c.1023C>A (p.His341Gln)	IL10RA-related disorder [RCV003403599]\|Inborn genetic diseases [RCV003243256]\|Inflammatory bowel disease 28 [RCV000689776]\|not provided [RCV004692105]	uncertain significance	11	117998927	117998927	Human	2	name , trait , alternate_id
13803462	CV573065	single nucleotide variant	NM_000628.5(IL10RB):c.727G>T (p.Ala243Ser)	IL10RB-related disorder [RCV003953243]\|Inflammatory bowel disease 25 [RCV000699258]\|not provided [RCV003480784]	likely benign\|uncertain significance	21	33288184	33288184	Human	1	name , trait , alternate_id
13832921	CV584147	single nucleotide variant	NM_001558.4(IL10RA):c.1260G>A (p.Ser420=)	IL10RA-related disorder [RCV003965504]\|Inflammatory bowel disease 28 [RCV001079569]\|not provided [RCV000728028]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	11	117999164	117999164	Human	1	name , trait , alternate_id
15158537	CV724212	single nucleotide variant	NM_001558.4(IL10RA):c.1638C>T (p.Ala546=)	IL10RA-related disorder [RCV003955824]\|Inflammatory bowel disease 28 [RCV000881025]	benign\|likely benign	11	117999542	117999542	Human	1	name , trait , alternate_id
15100205	CV728861	single nucleotide variant	NM_000628.5(IL10RB):c.483C>T (p.Asn161=)	IL10RB-related disorder [RCV003920776]\|Inflammatory bowel disease 25 [RCV000892069]	benign\|likely benign	21	33279903	33279903	Human	1	name , trait , alternate_id
15185163	CV742594	single nucleotide variant	NM_000628.5(IL10RB):c.763G>A (p.Ala255Thr)	IL10RB-related disorder [RCV003902841]\|Inflammatory bowel disease 25 [RCV000908453]	likely benign\|conflicting interpretations of pathogenicity	21	33288220	33288220	Human	1	name , trait , alternate_id
26902216	CV838015	single nucleotide variant	NM_001558.4(IL10RA):c.1057C>T (p.Pro353Ser)	IL10RA-related disorder [RCV003413892]\|Inflammatory bowel disease 28 [RCV001069197]	uncertain significance	11	117998961	117998961	Human	1	name , trait , alternate_id
126727358	CV1034883	single nucleotide variant	NM_000628.5(IL10RB):c.25C>T (p.Leu9=)	Inflammatory bowel disease 25 [RCV001348683]	likely benign\|uncertain significance	21	33266490	33266490	Human	1	name
127279078	CV1085637	single nucleotide variant	NM_000628.5(IL10RB):c.21C>T (p.Ser7=)	Inflammatory bowel disease 25 [RCV001408882]	likely benign	21	33266486	33266486	Human	1	name
127235341	CV1099533	single nucleotide variant	NM_001558.4(IL10RA):c.21G>A (p.Val7=)	Inflammatory bowel disease 28 [RCV001422253]	likely benign	11	117986488	117986488	Human	1	name
152074635	CV1647561	single nucleotide variant	NM_000628.5(IL10RB):c.27G>C (p.Leu9=)	Inflammatory bowel disease 25 [RCV002210432]	likely benign	21	33266492	33266492	Human	1	name
11641729	CV266227	single nucleotide variant	NM_001558.4(IL10RA):c.21G>C (p.Val7=)	Inflammatory bowel disease 28 [RCV000550448]\|not provided [RCV002274969]\|not specified [RCV000361895]	benign\|likely benign	11	117986488	117986488	Human	1	name
405171065	CV3055624	single nucleotide variant	NM_000628.5(IL10RB):c.27G>A (p.Leu9=)	Inflammatory bowel disease 25 [RCV003638511]	likely benign	21	33266492	33266492	Human	1	name
11659323	CV325206	single nucleotide variant	NM_001558.4(IL10RA):c.25C>T (p.Leu9=)	Inflammatory bowel disease 28 [RCV000356585]	uncertain significance	11	117986492	117986492	Human	1	name
127239886	CV1085638	single nucleotide variant	NM_000628.5(IL10RB):c.72C>T (p.Pro24=)	Inflammatory bowel disease 25 [RCV001397663]	likely benign	21	33268416	33268416	Human	1	name
127272235	CV1099534	single nucleotide variant	NM_001558.4(IL10RA):c.93T>C (p.Ser31=)	Inflammatory bowel disease 28 [RCV001431227]	likely benign	11	117988407	117988407	Human	1	name
151819179	CV1346693	single nucleotide variant	NM_000628.5(IL10RB):c.1A>C (p.Met1Leu)	Inflammatory bowel disease 25 [RCV001959667]	uncertain significance	21	33266466	33266466	Human	1	name
152126349	CV1533772	single nucleotide variant	NM_001558.4(IL10RA):c.45C>T (p.Leu15=)	Inflammatory bowel disease 28 [RCV002136367]	likely benign	11	117986512	117986512	Human	1	name
152123874	CV1587321	single nucleotide variant	NM_000628.5(IL10RB):c.39G>A (p.Leu13=)	Inflammatory bowel disease 25 [RCV002136063]	likely benign	21	33266504	33266504	Human	1	name
156437378	CV1937522	single nucleotide variant	NM_001558.4(IL10RA):c.30G>A (p.Ala10=)	Inflammatory bowel disease 28 [RCV003106913]	likely benign	11	117986497	117986497	Human	1	name
156434375	CV1940020	single nucleotide variant	NM_001558.4(IL10RA):c.87T>C (p.Pro29=)	Inflammatory bowel disease 28 [RCV003104434]	likely benign	11	117988401	117988401	Human	1	name
156321305	CV2067585	single nucleotide variant	NM_000628.5(IL10RB):c.51A>G (p.Ala17=)	Inflammatory bowel disease 25 [RCV002834714]	likely benign	21	33268395	33268395	Human	1	name
155972441	CV2135838	single nucleotide variant	NM_001558.4(IL10RA):c.81C>G (p.Pro27=)	Inflammatory bowel disease 28 [RCV002995691]	likely benign	11	117988395	117988395	Human	1	name
156111517	CV2146194	single nucleotide variant	NM_000628.5(IL10RB):c.5C>T (p.Ala2Val)	Inflammatory bowel disease 25 [RCV003021432]	uncertain significance	21	33266470	33266470	Human	1	name
156352505	CV2190459	single nucleotide variant	NM_000628.5(IL10RB):c.1A>T (p.Met1Leu)	Inflammatory bowel disease 25 [RCV003048441]	uncertain significance	21	33266466	33266466	Human	1	name
405005087	CV2873122	single nucleotide variant	NM_000628.5(IL10RB):c.40C>T (p.Leu14=)	Inflammatory bowel disease 25 [RCV003526713]	likely benign	21	33266505	33266505	Human	1	name
405116001	CV3119229	single nucleotide variant	NM_000628.5(IL10RB):c.52T>C (p.Leu18=)	Inflammatory bowel disease 25 [RCV003814265]	likely benign	21	33268396	33268396	Human	1	name
11610817	CV318321	single nucleotide variant	NM_001558.4(IL10RA):c.96G>A (p.Val32=)	Inflammatory bowel disease 28 [RCV001088383]\|not provided [RCV000593830]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	11	117988410	117988410	Human	1	name
11614486	CV324468	single nucleotide variant	NM_001558.4(IL10RA):c.72A>C (p.Thr24=)	Inflammatory bowel disease 28 [RCV000277188]\|not provided [RCV000596626]	conflicting interpretations of pathogenicity\|uncertain significance	11	117988386	117988386	Human	1	name
597920858	CV3738127	single nucleotide variant	NM_001558.4(IL10RA):c.63T>C (p.Ala21=)	Inflammatory bowel disease 28 [RCV005074726]	likely benign	11	117986530	117986530	Human	1	name
597916625	CV3779401	single nucleotide variant	NM_001558.4(IL10RA):c.3G>A (p.Met1Ile)	Inflammatory bowel disease 28 [RCV005129542]	pathogenic	11	117986470	117986470	Human	1	name
597947339	CV3800675	single nucleotide variant	NM_000628.5(IL10RB):c.69T>C (p.Pro23=)	Inflammatory bowel disease 25 [RCV005135075]	likely benign	21	33268413	33268413	Human	1	name
597936491	CV3862506	single nucleotide variant	NM_001558.4(IL10RA):c.72A>T (p.Thr24=)	Inflammatory bowel disease 28 [RCV005207778]	likely benign	11	117988386	117988386	Human	1	name
13490179	CV461716	single nucleotide variant	NM_001558.4(IL10RA):c.90G>A (p.Pro30=)	Inflammatory bowel disease 28 [RCV000533341]\|not provided [RCV004704083]	likely benign	11	117988404	117988404	Human	1	name
15202991	CV752446	single nucleotide variant	NM_001558.4(IL10RA):c.8C>A (p.Pro3Gln)	Inflammatory bowel disease 28 [RCV000913660]	likely benign	11	117986475	117986475	Human	1	name
38482811	CV926131	single nucleotide variant	NM_001558.4(IL10RA):c.8C>G (p.Pro3Arg)	Inflammatory bowel disease 28 [RCV001218593]	uncertain significance	11	117986475	117986475	Human	1	name
127231526	CV1077887	single nucleotide variant	NM_001558.4(IL10RA):c.282T>C (p.Asn94=)	Inflammatory bowel disease 28 [RCV001395358]	likely benign	11	117989535	117989535	Human	1	name
127252828	CV1085639	single nucleotide variant	NM_000628.5(IL10RB):c.177T>C (p.Tyr59=)	Inflammatory bowel disease 25 [RCV001418161]	likely benign	21	33276599	33276599	Human	1	name
127239310	CV1107361	single nucleotide variant	NM_000628.5(IL10RB):c.132T>A (p.Ala44=)	Inflammatory bowel disease 25 [RCV001433947]	likely benign	21	33268476	33268476	Human	1	name
127333644	CV1121080	single nucleotide variant	NM_001558.4(IL10RA):c.219C>T (p.Ser73=)	Inflammatory bowel disease 28 [RCV001473057]	likely benign	11	117989472	117989472	Human	1	name
127316090	CV1141920	single nucleotide variant	NM_001558.4(IL10RA):c.138A>G (p.Thr46=)	Inflammatory bowel disease 28 [RCV001502922]	likely benign	11	117988452	117988452	Human	1	name
127328018	CV1149713	single nucleotide variant	NM_000628.5(IL10RB):c.144G>C (p.Gly48=)	Inflammatory bowel disease 25 [RCV001506882]	likely benign	21	33268488	33268488	Human	1	name
127310301	CV1149714	single nucleotide variant	NM_000628.5(IL10RB):c.147C>T (p.Asn49=)	Inflammatory bowel disease 25 [RCV001481108]	likely benign	21	33268491	33268491	Human	1	name
151877485	CV1361432	single nucleotide variant	NM_001558.4(IL10RA):c.17T>C (p.Val6Ala)	Inflammatory bowel disease 28 [RCV001926006]	uncertain significance	11	117986484	117986484	Human	1	name
151796763	CV1403298	single nucleotide variant	NM_000628.5(IL10RB):c.207T>C (p.Thr69=)	Inflammatory bowel disease 25 [RCV001914455]	likely benign	21	33276629	33276629	Human	1	name
152096003	CV1559714	single nucleotide variant	NM_001558.4(IL10RA):c.126C>T (p.Ile42=)	Inflammatory bowel disease 28 [RCV002213365]	likely benign	11	117988440	117988440	Human	1	name
152093966	CV1634329	single nucleotide variant	NM_001558.4(IL10RA):c.120C>T (p.His40=)	Inflammatory bowel disease 28 [RCV002213108]	likely benign	11	117988434	117988434	Human	1	name
156417672	CV1909953	single nucleotide variant	NM_001558.4(IL10RA):c.13C>T (p.Leu5Phe)	Inflammatory bowel disease 28 [RCV002610842]	uncertain significance	11	117986480	117986480	Human	1	name
156354198	CV1933197	single nucleotide variant	NM_001558.4(IL10RA):c.262T>C (p.Leu88=)	Inflammatory bowel disease 28 [RCV002651136]	likely benign	11	117989515	117989515	Human	1	name
156446372	CV1937839	single nucleotide variant	NM_001558.4(IL10RA):c.177G>A (p.Val59=)	Inflammatory bowel disease 28 [RCV003117875]	likely benign	11	117988491	117988491	Human	1	name
156445931	CV1952182	single nucleotide variant	NM_000628.5(IL10RB):c.150G>A (p.Leu50=)	Inflammatory bowel disease 25 [RCV003116894]	likely benign	21	33268494	33268494	Human	1	name
155936034	CV2074840	single nucleotide variant	NM_001558.4(IL10RA):c.237G>C (p.Leu79=)	Inflammatory bowel disease 28 [RCV002861442]	likely benign	11	117989490	117989490	Human	1	name
156272531	CV2136626	single nucleotide variant	NM_000628.5(IL10RB):c.138C>T (p.Ala46=)	Inflammatory bowel disease 25 [RCV003009318]	likely benign	21	33268482	33268482	Human	1	name
156289054	CV2299286	single nucleotide variant	NM_000628.5(IL10RB):c.24G>T (p.Trp8Cys)	Inborn genetic diseases [RCV002878728]	uncertain significance	21	33266489	33266489	Human	1	name
405185198	CV2997293	single nucleotide variant	NM_001558.4(IL10RA):c.132C>T (p.His44=)	Inflammatory bowel disease 28 [RCV003640141]	likely benign	11	117988446	117988446	Human	1	name
11602343	CV312438	single nucleotide variant	NM_001558.4(IL10RA):c.144C>T (p.Ile48=)	Inflammatory bowel disease 28 [RCV000647209]	benign\|likely benign\|uncertain significance	11	117988458	117988458	Human	1	name
405143370	CV3125998	single nucleotide variant	NM_000628.5(IL10RB):c.144G>A (p.Gly48=)	Inflammatory bowel disease 25 [RCV003816914]	likely benign	21	33268488	33268488	Human	1	name
11621335	CV325208	single nucleotide variant	NM_001558.4(IL10RA):c.180G>A (p.Ala60=)	Inflammatory bowel disease 28 [RCV000347549]\|not provided [RCV004706793]\|not specified [RCV003401292]	benign\|likely benign	11	117988494	117988494	Human	1	name
597834914	CV3760863	single nucleotide variant	NM_001558.4(IL10RA):c.216C>T (p.Ile72=)	Inflammatory bowel disease 28 [RCV005085414]	likely benign	11	117989469	117989469	Human	1	name
597974656	CV3802300	single nucleotide variant	NM_001558.4(IL10RA):c.267C>T (p.Asp89=)	Inflammatory bowel disease 28 [RCV005144077]	likely benign	11	117989520	117989520	Human	1	name
13620004	CV525919	single nucleotide variant	NM_001558.4(IL10RA):c.252C>T (p.Thr84=)	Inflammatory bowel disease 28 [RCV000647214]	likely benign	11	117989505	117989505	Human	1	name
14699164	CV624689	deletion	NM_000628.5(IL10RB):c.53del (p.Leu18fs)	not provided [RCV000788409]	likely pathogenic	21	33268396	33268396	Human		name
14726421	CV639722	single nucleotide variant	NM_001558.4(IL10RA):c.16G>C (p.Val6Leu)	Inflammatory bowel disease 28 [RCV000815632]	uncertain significance	11	117986483	117986483	Human	1	name
15105893	CV773295	single nucleotide variant	NM_000628.5(IL10RB):c.123G>A (p.Glu41=)	Inflammatory bowel disease 25 [RCV000937678]\|not provided [RCV003438601]	likely benign	21	33268467	33268467	Human	1	name
15193934	CV773297	single nucleotide variant	NM_000628.5(IL10RB):c.259T>C (p.Leu87=)	Inflammatory bowel disease 25 [RCV002066123]	likely benign	21	33276681	33276681	Human	1	name
26921250	CV838005	single nucleotide variant	NM_001558.4(IL10RA):c.20T>A (p.Val7Glu)	Inflammatory bowel disease 28 [RCV001049526]	uncertain significance	11	117986487	117986487	Human	1	name
38485815	CV929304	single nucleotide variant	NM_000628.5(IL10RB):c.20G>A (p.Ser7Asn)	Inflammatory bowel disease 25 [RCV001220017]	uncertain significance	21	33266485	33266485	Human	1	name
126749226	CV1014316	single nucleotide variant	NM_000628.5(IL10RB):c.91T>A (p.Ser31Thr)	Inflammatory bowel disease 25 [RCV001326491]	uncertain significance	21	33268435	33268435	Human	1	name
126756581	CV1030075	single nucleotide variant	NM_001558.4(IL10RA):c.37C>T (p.Leu13Phe)	Inflammatory bowel disease 28 [RCV001339319]	uncertain significance	11	117986504	117986504	Human	1	name
127237067	CV1077889	single nucleotide variant	NM_001558.4(IL10RA):c.741C>T (p.Ser247=)	Inflammatory bowel disease 28 [RCV001392221]	likely benign	11	117995641	117995641	Human	1	name
127276974	CV1077890	single nucleotide variant	NM_001558.4(IL10RA):c.942C>T (p.His314=)	Inflammatory bowel disease 28 [RCV001407484]	likely benign	11	117998846	117998846	Human	1	name
127282920	CV1077891	single nucleotide variant	NM_001558.4(IL10RA):c.972C>G (p.Thr324=)	Inflammatory bowel disease 28 [RCV001411462]	likely benign	11	117998876	117998876	Human	1	name
127230963	CV1077892	single nucleotide variant	NM_001558.4(IL10RA):c.999C>T (p.Pro333=)	Inflammatory bowel disease 28 [RCV001412823]	likely benign	11	117998903	117998903	Human	1	name
127279668	CV1085640	single nucleotide variant	NM_000628.5(IL10RB):c.420C>T (p.Tyr140=)	Inflammatory bowel disease 25 [RCV001409273]	likely benign	21	33279840	33279840	Human	1	name
127231246	CV1085641	single nucleotide variant	NM_000628.5(IL10RB):c.681C>T (p.Leu227=)	Inflammatory bowel disease 25 [RCV001395202]	likely benign	21	33288138	33288138	Human	1	name
127241556	CV1085642	single nucleotide variant	NM_000628.5(IL10RB):c.762C>T (p.Tyr254=)	Inflammatory bowel disease 25 [RCV001398010]	likely benign	21	33288219	33288219	Human	1	name
127250660	CV1099535	single nucleotide variant	NM_001558.4(IL10RA):c.378A>T (p.Thr126=)	Inflammatory bowel disease 28 [RCV001425415]	likely benign	11	117993251	117993251	Human	1	name
127265953	CV1107362	single nucleotide variant	NM_000628.5(IL10RB):c.432T>A (p.Thr144=)	Inflammatory bowel disease 25 [RCV001429272]	likely benign	21	33279852	33279852	Human	1	name
127270964	CV1107363	single nucleotide variant	NM_000628.5(IL10RB):c.966G>T (p.Gly322=)	Inflammatory bowel disease 25 [RCV001430786]	likely benign	21	33296345	33296345	Human	1	name
127290097	CV1121081	single nucleotide variant	NM_001558.4(IL10RA):c.301C>A (p.Arg101=)	Inflammatory bowel disease 28 [RCV001458344]\|not provided [RCV001773750]	likely benign\|uncertain significance	11	117989554	117989554	Human	1	name
127317989	CV1121082	single nucleotide variant	NM_001558.4(IL10RA):c.474A>G (p.Glu158=)	Inflammatory bowel disease 28 [RCV001466046]	likely benign	11	117993347	117993347	Human	1	name
127329556	CV1121083	single nucleotide variant	NM_001558.4(IL10RA):c.495A>C (p.Arg165=)	Inflammatory bowel disease 28 [RCV001470302]	likely benign	11	117993368	117993368	Human	1	name
127298048	CV1128771	single nucleotide variant	NM_000628.5(IL10RB):c.657C>T (p.Pro219=)	Inflammatory bowel disease 25 [RCV001453198]	likely benign	21	33288114	33288114	Human	1	name
127288211	CV1128772	single nucleotide variant	NM_000628.5(IL10RB):c.717C>T (p.Leu239=)	Inflammatory bowel disease 25 [RCV001450401]	likely benign	21	33288174	33288174	Human	1	name
127290375	CV1128773	single nucleotide variant	NM_000628.5(IL10RB):c.888T>C (p.Ser296=)	Inflammatory bowel disease 25 [RCV001458421]	likely benign	21	33296267	33296267	Human	1	name
127333629	CV1141921	single nucleotide variant	NM_001558.4(IL10RA):c.423G>A (p.Gly141=)	Inflammatory bowel disease 28 [RCV001490299]	likely benign	11	117993296	117993296	Human	1	name
127295937	CV1141922	single nucleotide variant	NM_001558.4(IL10RA):c.678C>T (p.Leu226=)	Inflammatory bowel disease 28 [RCV001497368]	likely benign	11	117994139	117994139	Human	1	name
127317306	CV1141923	single nucleotide variant	NM_001558.4(IL10RA):c.813C>G (p.Leu271=)	Inflammatory bowel disease 28 [RCV001503351]	likely benign	11	117998717	117998717	Human	1	name
127302902	CV1141924	single nucleotide variant	NM_001558.4(IL10RA):c.885G>A (p.Pro295=)	Inflammatory bowel disease 28 [RCV001479089]\|not provided [RCV004704603]	likely benign	11	117998789	117998789	Human	1	name
127305302	CV1149715	single nucleotide variant	NM_000628.5(IL10RB):c.630G>A (p.Glu210=)	Inflammatory bowel disease 25 [RCV001499880]	likely benign	21	33283225	33283225	Human	1	name
127329349	CV1149716	single nucleotide variant	NM_000628.5(IL10RB):c.822T>C (p.His274=)	Inflammatory bowel disease 25 [RCV001487363]	likely benign	21	33296201	33296201	Human	1	name
151743674	CV1401417	single nucleotide variant	NM_001558.4(IL10RA):c.65A>C (p.His22Pro)	Inflammatory bowel disease 28 [RCV001947356]	uncertain significance	11	117986532	117986532	Human	1	name
151819230	CV1405936	single nucleotide variant	NM_000628.5(IL10RB):c.35G>A (p.Cys12Tyr)	Inflammatory bowel disease 25 [RCV001959718]	uncertain significance	21	33266500	33266500	Human	1	name
151804094	CV1418602	single nucleotide variant	NM_000628.5(IL10RB):c.85A>G (p.Met29Val)	Inborn genetic diseases [RCV002558492]\|Inflammatory bowel disease 25 [RCV001928911]	uncertain significance	21	33268429	33268429	Human	2	name
152077593	CV1531346	single nucleotide variant	NM_001558.4(IL10RA):c.336C>G (p.Thr112=)	Inflammatory bowel disease 28 [RCV002210801]	likely benign	11	117989589	117989589	Human	1	name
152089856	CV1563173	single nucleotide variant	NM_000628.5(IL10RB):c.735G>A (p.Leu245=)	Inflammatory bowel disease 25 [RCV002113925]	likely benign	21	33288192	33288192	Human	1	name
152067168	CV1566771	single nucleotide variant	NM_000628.5(IL10RB):c.966G>A (p.Gly322=)	Inflammatory bowel disease 25 [RCV002091078]	likely benign	21	33296345	33296345	Human	1	name
152048000	CV1569654	single nucleotide variant	NM_000628.5(IL10RB):c.360A>G (p.Val120=)	Inflammatory bowel disease 25 [RCV002126877]	likely benign	21	33279780	33279780	Human	1	name
152166696	CV1597133	single nucleotide variant	NM_000628.5(IL10RB):c.312C>T (p.Thr104=)	Inflammatory bowel disease 25 [RCV002204498]	likely benign	21	33276734	33276734	Human	1	name
152174479	CV1601985	single nucleotide variant	NM_001558.4(IL10RA):c.684G>A (p.Arg228=)	Inflammatory bowel disease 28 [RCV002144450]	likely benign	11	117994145	117994145	Human	1	name
152041923	CV1603324	single nucleotide variant	NM_000628.5(IL10RB):c.954G>A (p.Pro318=)	Inflammatory bowel disease 25 [RCV002071133]	conflicting interpretations of pathogenicity	21	33296333	33296333	Human	1	name
152099815	CV1627332	single nucleotide variant	NM_001558.4(IL10RA):c.804T>C (p.Ser268=)	Inflammatory bowel disease 28 [RCV002095372]	likely benign	11	117995704	117995704	Human	1	name
152141208	CV1630398	single nucleotide variant	NM_001558.4(IL10RA):c.465C>T (p.Asp155=)	Inflammatory bowel disease 28 [RCV002120398]	likely benign	11	117993338	117993338	Human	1	name
152034340	CV1634882	single nucleotide variant	NM_001558.4(IL10RA):c.792G>A (p.Lys264=)	Inflammatory bowel disease 28 [RCV002086955]	likely benign	11	117995692	117995692	Human	1	name
152079841	CV1649798	single nucleotide variant	NM_001558.4(IL10RA):c.798A>G (p.Leu266=)	Inflammatory bowel disease 28 [RCV002092701]	likely benign	11	117995698	117995698	Human	1	name
152043381	CV1650819	single nucleotide variant	NM_000628.5(IL10RB):c.891C>T (p.Val297=)	Inflammatory bowel disease 25 [RCV002165983]	likely benign	21	33296270	33296270	Human	1	name
155641381	CV1709743	single nucleotide variant	NM_001558.4(IL10RA):c.540C>T (p.Phe180=)	not provided [RCV002292843]	likely benign	11	117994001	117994001	Human		name
156262158	CV1913608	single nucleotide variant	NM_000628.5(IL10RB):c.636A>C (p.Thr212=)	Inflammatory bowel disease 25 [RCV002627801]	likely benign	21	33283231	33283231	Human	1	name
156027676	CV1918947	single nucleotide variant	NM_000628.5(IL10RB):c.741C>T (p.Cys247=)	Inflammatory bowel disease 25 [RCV002637019]	likely benign	21	33288198	33288198	Human	1	name
156303692	CV1934608	single nucleotide variant	NM_000628.5(IL10RB):c.912C>T (p.Ser304=)	Inflammatory bowel disease 25 [RCV002647772]	likely benign	21	33296291	33296291	Human	1	name
156298825	CV1955456	single nucleotide variant	NM_000628.5(IL10RB):c.450C>T (p.Asn150=)	Inflammatory bowel disease 25 [RCV002578136]	likely benign	21	33279870	33279870	Human	1	name
156151990	CV1961077	single nucleotide variant	NM_000628.5(IL10RB):c.651G>A (p.Thr217=)	Inflammatory bowel disease 25 [RCV002572928]	uncertain significance	21	33288108	33288108	Human	1	name
156414815	CV1983016	single nucleotide variant	NM_001558.4(IL10RA):c.71C>A (p.Thr24Lys)	Inborn genetic diseases [RCV004065815]\|Inflammatory bowel disease 28 [RCV002609377]	uncertain significance	11	117988385	117988385	Human	2	name
156302380	CV1998497	single nucleotide variant	NM_001558.4(IL10RA):c.594G>A (p.Val198=)	Inflammatory bowel disease 28 [RCV002671219]	likely benign	11	117994055	117994055	Human	1	name
156010294	CV2042871	single nucleotide variant	NM_000628.5(IL10RB):c.672C>T (p.Ala224=)	Inflammatory bowel disease 25 [RCV002756646]	likely benign	21	33288129	33288129	Human	1	name
156050268	CV2060019	single nucleotide variant	NM_000628.5(IL10RB):c.60G>A (p.Met20Ile)	Inborn genetic diseases [RCV005351025]\|Inflammatory bowel disease 25 [RCV002796743]	uncertain significance	21	33268404	33268404	Human	2	name
156328662	CV2094626	single nucleotide variant	NM_001558.4(IL10RA):c.318C>T (p.Ser106=)	Inflammatory bowel disease 28 [RCV002899786]	likely benign	11	117989571	117989571	Human	1	name
156002906	CV2106873	single nucleotide variant	NM_000628.5(IL10RB):c.444G>C (p.Val148=)	Inflammatory bowel disease 25 [RCV002947874]	likely benign	21	33279864	33279864	Human	1	name
156209611	CV2114329	single nucleotide variant	NM_001558.4(IL10RA):c.660A>G (p.Lys220=)	Inflammatory bowel disease 28 [RCV002932007]	likely benign	11	117994121	117994121	Human	1	name
156234988	CV2118373	single nucleotide variant	NM_000628.5(IL10RB):c.444G>A (p.Val148=)	Inflammatory bowel disease 25 [RCV002958657]	likely benign	21	33279864	33279864	Human	1	name
156390693	CV2122472	single nucleotide variant	NM_001558.4(IL10RA):c.44T>C (p.Leu15Pro)	Inflammatory bowel disease 28 [RCV002943874]	uncertain significance	11	117986511	117986511	Human	1	name
156283658	CV2133976	single nucleotide variant	NM_000628.5(IL10RB):c.29G>C (p.Gly10Ala)	Inborn genetic diseases [RCV004983262]\|Inflammatory bowel disease 25 [RCV003009687]	uncertain significance	21	33266494	33266494	Human	2	name
156119934	CV2151648	single nucleotide variant	NM_000628.5(IL10RB):c.660C>G (p.Ser220=)	Inflammatory bowel disease 25 [RCV003002939]	likely benign	21	33288117	33288117	Human	1	name
156334450	CV2181959	single nucleotide variant	NM_001558.4(IL10RA):c.717C>T (p.Phe239=)	Inflammatory bowel disease 28 [RCV003047400]	likely benign	11	117995617	117995617	Human	1	name
156365070	CV2192041	single nucleotide variant	NM_000628.5(IL10RB):c.726C>T (p.Phe242=)	Inflammatory bowel disease 25 [RCV003065896]	likely benign	21	33288183	33288183	Human	1	name
11580277	CV270570	single nucleotide variant	NM_001558.4(IL10RA):c.931T>C (p.Leu311=)	Inflammatory bowel disease 28 [RCV001079433]\|not provided [RCV000281135]	benign\|conflicting interpretations of pathogenicity\|uncertain significance	11	117998835	117998835	Human	1	name
404995515	CV2855861	single nucleotide variant	NM_000628.5(IL10RB):c.702C>T (p.Val234=)	Inflammatory bowel disease 25 [RCV003525604]	likely benign	21	33288159	33288159	Human	1	name
405005235	CV2880193	single nucleotide variant	NM_001558.4(IL10RA):c.627C>T (p.Val209=)	Inflammatory bowel disease 28 [RCV003526725]	likely benign	11	117994088	117994088	Human	1	name
405006230	CV2884624	single nucleotide variant	NM_000628.5(IL10RB):c.945C>T (p.Leu315=)	Inflammatory bowel disease 25 [RCV003526815]	likely benign	21	33296324	33296324	Human	1	name
405001850	CV2925353	single nucleotide variant	NM_000628.5(IL10RB):c.498G>A (p.Lys166=)	Inflammatory bowel disease 25 [RCV003526397]	uncertain significance	21	33279918	33279918	Human	1	name
405178948	CV2939379	single nucleotide variant	NM_001558.4(IL10RA):c.627C>A (p.Val209=)	Inflammatory bowel disease 28 [RCV003639422]	likely benign	11	117994088	117994088	Human	1	name
405179447	CV2960518	single nucleotide variant	NM_000628.5(IL10RB):c.561T>C (p.Tyr187=)	Inflammatory bowel disease 25 [RCV003639472]	likely benign	21	33283156	33283156	Human	1	name
405182379	CV2977901	single nucleotide variant	NM_001558.4(IL10RA):c.582C>G (p.Thr194=)	Inflammatory bowel disease 28 [RCV003639813]	likely benign	11	117994043	117994043	Human	1	name
405182327	CV2980968	single nucleotide variant	NM_001558.4(IL10RA):c.555A>G (p.Val185=)	Inflammatory bowel disease 28 [RCV003639807]	likely benign	11	117994016	117994016	Human	1	name
405182468	CV2981379	single nucleotide variant	NM_001558.4(IL10RA):c.300G>A (p.Val100=)	Inflammatory bowel disease 28 [RCV003639824]	likely benign	11	117989553	117989553	Human	1	name
405184066	CV3001680	single nucleotide variant	NM_000628.5(IL10RB):c.834T>A (p.Leu278=)	Inflammatory bowel disease 25 [RCV003640007]	likely benign	21	33296213	33296213	Human	1	name
405185412	CV3004398	single nucleotide variant	NM_000628.5(IL10RB):c.831A>G (p.Thr277=)	Inflammatory bowel disease 25 [RCV003640164]	likely benign	21	33296210	33296210	Human	1	name
405168845	CV3033723	single nucleotide variant	NM_000628.5(IL10RB):c.796C>T (p.Leu266=)	Inflammatory bowel disease 25 [RCV003638312]	likely benign	21	33288253	33288253	Human	1	name
405168310	CV3040678	single nucleotide variant	NM_000628.5(IL10RB):c.372T>G (p.Ala124=)	Inflammatory bowel disease 25 [RCV003638263]	likely benign	21	33279792	33279792	Human	1	name
405170744	CV3055145	single nucleotide variant	NM_000628.5(IL10RB):c.849T>C (p.Phe283=)	Inflammatory bowel disease 25 [RCV003638482]	likely benign	21	33296228	33296228	Human	1	name
405176566	CV3062122	single nucleotide variant	NM_000628.5(IL10RB):c.555A>G (p.Thr185=)	Inflammatory bowel disease 25 [RCV003639125]	likely benign	21	33283150	33283150	Human	1	name
405177956	CV3071975	single nucleotide variant	NM_000628.5(IL10RB):c.594G>A (p.Arg198=)	Inflammatory bowel disease 25 [RCV003639320]	likely benign	21	33283189	33283189	Human	1	name
405177241	CV3076397	single nucleotide variant	NM_001558.4(IL10RA):c.936C>T (p.Asp312=)	Inflammatory bowel disease 28 [RCV003639243]	likely benign	11	117998840	117998840	Human	1	name
405160866	CV3125071	single nucleotide variant	NM_001558.4(IL10RA):c.927G>A (p.Lys309=)	Inflammatory bowel disease 28 [RCV003818342]	likely benign	11	117998831	117998831	Human	1	name
405140615	CV3125774	single nucleotide variant	NM_000628.5(IL10RB):c.759G>A (p.Lys253=)	Inflammatory bowel disease 25 [RCV003816689]	likely benign	21	33288216	33288216	Human	1	name
405114367	CV3133870	single nucleotide variant	NM_001558.4(IL10RA):c.456C>T (p.Pro152=)	Inflammatory bowel disease 28 [RCV003836665]	likely benign	11	117993329	117993329	Human	1	name
405252385	CV3177942	single nucleotide variant	NM_000628.5(IL10RB):c.549A>G (p.Pro183=)	Inflammatory bowel disease 25 [RCV003870722]	likely benign	21	33283144	33283144	Human	1	name
405231203	CV3180898	single nucleotide variant	NM_001558.4(IL10RA):c.861A>G (p.Pro287=)	Inflammatory bowel disease 28 [RCV003865136]	likely benign	11	117998765	117998765	Human	1	name
11603131	CV318326	single nucleotide variant	NM_001558.4(IL10RA):c.459A>G (p.Ala153=)	Inflammatory bowel disease 28 [RCV000297163]\|not provided [RCV001824728]\|not specified [RCV000454846]	benign\|not provided	11	117993332	117993332	Human	1	name
11625329	CV324473	single nucleotide variant	NM_001558.4(IL10RA):c.447G>A (p.Lys149=)	Inflammatory bowel disease 28 [RCV000397670]	uncertain significance	11	117993320	117993320	Human	1	name
11612748	CV324476	single nucleotide variant	NM_001558.4(IL10RA):c.525G>A (p.Pro175=)	Inflammatory bowel disease 28 [RCV000261984]\|not provided [RCV004706794]	benign	11	117993398	117993398	Human	1	name
11622985	CV324477	single nucleotide variant	NM_001558.4(IL10RA):c.696C>T (p.Thr232=)	Inflammatory bowel disease 28 [RCV000625086]\|not provided [RCV001091035]\|not specified [RCV000734742]	benign\|likely benign\|uncertain significance	11	117995596	117995596	Human	1	name
11624194	CV324483	single nucleotide variant	NM_001558.4(IL10RA):c.972C>T (p.Thr324=)	Inflammatory bowel disease 28 [RCV000544267]\|not provided [RCV004706795]	benign\|likely benign	11	117998876	117998876	Human	1	name
11619826	CV325207	single nucleotide variant	NM_001558.4(IL10RA):c.80C>T (p.Pro27Leu)	Inborn genetic diseases [RCV004021497]\|Inflammatory bowel disease 28 [RCV000330022]	uncertain significance	11	117988394	117988394	Human	2	name
11617521	CV325215	single nucleotide variant	NM_001558.4(IL10RA):c.336C>T (p.Thr112=)	Inborn genetic diseases [RCV004984797]\|Inflammatory bowel disease 28 [RCV000305533]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	11	117989589	117989589	Human	2	name
597699684	CV3690116	single nucleotide variant	NM_001558.4(IL10RA):c.94G>A (p.Val32Met)	Inborn genetic diseases [RCV004987789]	uncertain significance	11	117988408	117988408	Human	1	name
597930743	CV3789376	single nucleotide variant	NM_001558.4(IL10RA):c.606T>C (p.Cys202=)	Inflammatory bowel disease 28 [RCV005131657]	likely benign	11	117994067	117994067	Human	1	name
597847906	CV3792879	single nucleotide variant	NM_001558.4(IL10RA):c.85C>G (p.Pro29Ala)	Inflammatory bowel disease 28 [RCV005145015]	uncertain significance	11	117988399	117988399	Human	1	name
597948824	CV3801257	single nucleotide variant	NM_001558.4(IL10RA):c.319C>A (p.Arg107=)	Inflammatory bowel disease 28 [RCV005135437]	likely benign	11	117989572	117989572	Human	1	name
597866172	CV3802789	single nucleotide variant	NM_001558.4(IL10RA):c.912G>A (p.Val304=)	Inflammatory bowel disease 28 [RCV005147576]	uncertain significance	11	117998816	117998816	Human	1	name
597914198	CV3833897	single nucleotide variant	NM_001558.4(IL10RA):c.702C>T (p.Thr234=)	Inflammatory bowel disease 28 [RCV005183256]	likely benign	11	117995602	117995602	Human	1	name
597884538	CV3834957	single nucleotide variant	NM_000628.5(IL10RB):c.798G>A (p.Leu266=)	Inflammatory bowel disease 25 [RCV005178681]	likely benign	21	33288255	33288255	Human	1	name
597906528	CV3853468	single nucleotide variant	NM_001558.4(IL10RA):c.99G>A (p.Trp33Ter)	Inflammatory bowel disease 28 [RCV005202946]	pathogenic	11	117988413	117988413	Human	1	name
13619995	CV525995	single nucleotide variant	NM_001558.4(IL10RA):c.420C>T (p.Leu140=)	Inflammatory bowel disease 28 [RCV000647206]	likely benign	11	117993293	117993293	Human	1	name
13620001	CV526079	single nucleotide variant	NM_001558.4(IL10RA):c.75G>T (p.Glu25Asp)	Inflammatory bowel disease 28 [RCV000647212]\|not provided [RCV001702540]\|not specified [RCV001726289]	benign\|likely benign	11	117988389	117988389	Human	1	name
13618305	CV533820	single nucleotide variant	NM_000628.5(IL10RB):c.768C>T (p.Phe256=)	Inflammatory bowel disease 25 [RCV000645974]	likely benign	21	33288225	33288225	Human	1	name
13618307	CV534377	single nucleotide variant	NM_000628.5(IL10RB):c.465T>C (p.Asn155=)	Inflammatory bowel disease 25 [RCV000645975]\|not provided [RCV004717700]	benign	21	33279885	33279885	Human	1	name
14704851	CV639729	single nucleotide variant	NM_001558.4(IL10RA):c.762G>A (p.Leu254=)	Inflammatory bowel disease 28 [RCV000791494]	likely benign\|uncertain significance	11	117995662	117995662	Human	1	name
15185941	CV724211	single nucleotide variant	NM_001558.4(IL10RA):c.937C>T (p.Leu313=)	Inflammatory bowel disease 28 [RCV000886836]	likely benign	11	117998841	117998841	Human	1	name
15189442	CV737751	single nucleotide variant	NM_001558.4(IL10RA):c.633C>T (p.Ser211=)	Inflammatory bowel disease 28 [RCV000909650]	likely benign	11	117994094	117994094	Human	1	name
15158267	CV752447	single nucleotide variant	NM_001558.4(IL10RA):c.954C>T (p.Asp318=)	Inflammatory bowel disease 28 [RCV000925034]	likely benign	11	117998858	117998858	Human	1	name
15120988	CV757751	single nucleotide variant	NM_000628.5(IL10RB):c.645C>T (p.Asp215=)	Inflammatory bowel disease 25 [RCV000918406]	benign\|conflicting interpretations of pathogenicity	21	33283240	33283240	Human	1	name
15123687	CV768220	single nucleotide variant	NM_001558.4(IL10RA):c.723C>T (p.Ala241=)	Inflammatory bowel disease 28 [RCV000940898]	likely benign	11	117995623	117995623	Human	1	name
15102588	CV783874	single nucleotide variant	NM_001558.4(IL10RA):c.789A>G (p.Arg263=)	Inflammatory bowel disease 28 [RCV001447102]	likely benign	11	117995689	117995689	Human	1	name
25315126	CV818393	single nucleotide variant	NM_001558.4(IL10RA):c.537G>A (p.Thr179=)	Inflammatory bowel disease 28 [RCV001030031]	pathogenic\|likely pathogenic	11	117993410	117993410	Human	1	name
26913217	CV838006	single nucleotide variant	NM_001558.4(IL10RA):c.46C>T (p.Arg16Cys)	Inflammatory bowel disease 28 [RCV001035429]	uncertain significance	11	117986513	117986513	Human	1	name
26886395	CV838007	single nucleotide variant	NM_001558.4(IL10RA):c.47G>C (p.Arg16Pro)	Inborn genetic diseases [RCV004031735]\|Inflammatory bowel disease 28 [RCV001054870]	uncertain significance	11	117986514	117986514	Human	2	name
26906187	CV848721	single nucleotide variant	NM_000628.5(IL10RB):c.79G>C (p.Val27Leu)	Inflammatory bowel disease 25 [RCV001051605]	uncertain significance	21	33268423	33268423	Human	1	name
28904428	CV867070	single nucleotide variant	NM_001558.4(IL10RA):c.89C>T (p.Pro30Leu)	Inflammatory bowel disease 28 [RCV001105571]\|not provided [RCV003326540]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	11	117988403	117988403	Human	1	name
8633866	CV89082	single nucleotide variant	NM_001558.4(IL10RA):c.750C>T (p.Leu250=)	Inflammatory bowel disease 28 [RCV002653195]	likely benign\|not provided	11	117995650	117995650	Human	1	name
38469125	CV939086	single nucleotide variant	NM_000628.5(IL10RB):c.690G>A (p.Ser230=)	Inflammatory bowel disease 25 [RCV001202238]	likely benign\|uncertain significance	21	33288147	33288147	Human	1	name
38483825	CV947330	single nucleotide variant	NM_001558.4(IL10RA):c.477C>T (p.Ser159=)	Inflammatory bowel disease 28 [RCV001236087]	likely benign\|uncertain significance	11	117993350	117993350	Human	1	name
126767347	CV999164	single nucleotide variant	NM_000628.5(IL10RB):c.804G>A (p.Glu268=)	Inflammatory bowel disease 25 [RCV001302248]	uncertain significance	21	33288261	33288261	Human	1	name
126736804	CV1000716	single nucleotide variant	NM_001558.4(IL10RA):c.1026C>G (p.Pro342=)	Inflammatory bowel disease 28 [RCV002071867]\|not provided [RCV001311791]	likely benign	11	117998930	117998930	Human	1	name
126764469	CV1034886	deletion	NM_000628.5(IL10RB):c.832del (p.Leu278fs)	Inflammatory bowel disease 25 [RCV001341667]	uncertain significance	21	33296211	33296211	Human	1	name
126920935	CV1047047	single nucleotide variant	NM_001558.4(IL10RA):c.253G>A (p.Ala85Thr)	Inflammatory bowel disease 28 [RCV001363176]\|not provided [RCV003238362]	uncertain significance	11	117989506	117989506	Human	1	name
127258095	CV1077893	single nucleotide variant	NM_001558.4(IL10RA):c.1326A>G (p.Ala442=)	Inflammatory bowel disease 28 [RCV001401625]	likely benign	11	117999230	117999230	Human	1	name
127284194	CV1099536	single nucleotide variant	NM_001558.4(IL10RA):c.1066C>T (p.Leu356=)	Inflammatory bowel disease 28 [RCV001449072]	likely benign	11	117998970	117998970	Human	1	name
127243860	CV1099537	single nucleotide variant	NM_001558.4(IL10RA):c.1140C>T (p.Ser380=)	Inflammatory bowel disease 28 [RCV001424028]	likely benign	11	117999044	117999044	Human	1	name
127233310	CV1099538	single nucleotide variant	NM_001558.4(IL10RA):c.1158C>T (p.Thr386=)	Inflammatory bowel disease 28 [RCV001421720]	likely benign	11	117999062	117999062	Human	1	name
127259030	CV1099539	single nucleotide variant	NM_001558.4(IL10RA):c.1284G>A (p.Pro428=)	Inflammatory bowel disease 28 [RCV001438281]	likely benign	11	117999188	117999188	Human	1	name
127273780	CV1099540	single nucleotide variant	NM_001558.4(IL10RA):c.1722G>T (p.Leu574=)	Inflammatory bowel disease 28 [RCV001442682]	likely benign	11	117999626	117999626	Human	1	name
127327903	CV1141925	single nucleotide variant	NM_001558.4(IL10RA):c.1038A>G (p.Arg346=)	Inflammatory bowel disease 28 [RCV001506843]	likely benign	11	117998942	117998942	Human	1	name
127300945	CV1141926	single nucleotide variant	NM_001558.4(IL10RA):c.1620C>T (p.Ser540=)	Inflammatory bowel disease 28 [RCV001498702]	likely benign	11	117999524	117999524	Human	1	name
151786673	CV1360904	single nucleotide variant	NM_000628.5(IL10RB):c.107A>C (p.Asn36Thr)	Inflammatory bowel disease 25 [RCV001894310]	uncertain significance	21	33268451	33268451	Human	1	name
151857804	CV1363915	single nucleotide variant	NM_001558.4(IL10RA):c.1458C>T (p.Gly486=)	Inflammatory bowel disease 28 [RCV001904906]	likely benign\|uncertain significance	11	117999362	117999362	Human	1	name
151871583	CV1392791	single nucleotide variant	NM_001558.4(IL10RA):c.290G>A (p.Arg97Gln)	Inflammatory bowel disease 28 [RCV001925292]	uncertain significance	11	117989543	117989543	Human	1	name
151810115	CV1396930	single nucleotide variant	NM_000628.5(IL10RB):c.122A>G (p.Glu41Gly)	Inflammatory bowel disease 25 [RCV001940284]	uncertain significance	21	33268466	33268466	Human	1	name
151782937	CV1422371	duplication	NM_001558.4(IL10RA):c.618dup (p.Pro207fs)	Inflammatory bowel disease 28 [RCV001972249]	pathogenic	11	117994076	117994077	Human	1	name
151750663	CV1457243	single nucleotide variant	NM_001558.4(IL10RA):c.184C>A (p.Leu62Met)	Inflammatory bowel disease 28 [RCV001912952]	uncertain significance	11	117988498	117988498	Human	1	name
151887454	CV1471987	single nucleotide variant	NM_001558.4(IL10RA):c.158A>C (p.Glu53Ala)	Inflammatory bowel disease 28 [RCV002000884]	uncertain significance	11	117988472	117988472	Human	1	name
151832449	CV1500908	single nucleotide variant	NM_000628.5(IL10RB):c.194A>G (p.Lys65Arg)	Inflammatory bowel disease 25 [RCV001987140]	uncertain significance	21	33276616	33276616	Human	1	name
151711245	CV1515127	single nucleotide variant	NM_000628.5(IL10RB):c.274G>C (p.Glu92Gln)	Inflammatory bowel disease 25 [RCV002001676]	uncertain significance	21	33276696	33276696	Human	1	name
152122231	CV1521578	single nucleotide variant	NM_001558.4(IL10RA):c.1716T>C (p.Ser572=)	Inflammatory bowel disease 28 [RCV002135855]	likely benign	11	117999620	117999620	Human	1	name
152129580	CV1538983	single nucleotide variant	NM_001558.4(IL10RA):c.1482G>A (p.Lys494=)	Inflammatory bowel disease 28 [RCV002217882]	likely benign	11	117999386	117999386	Human	1	name
152088882	CV1541454	single nucleotide variant	NM_001558.4(IL10RA):c.1695G>T (p.Leu565=)	Inflammatory bowel disease 28 [RCV002171564]	likely benign	11	117999599	117999599	Human	1	name
152101615	CV1578914	single nucleotide variant	NM_001558.4(IL10RA):c.1197T>C (p.Asp399=)	Inflammatory bowel disease 28 [RCV002079068]\|not provided [RCV003222394]	likely benign	11	117999101	117999101	Human	1	name
152130355	CV1582240	single nucleotide variant	NM_001558.4(IL10RA):c.1392G>A (p.Glu464=)	Inflammatory bowel disease 28 [RCV002099401]	likely benign	11	117999296	117999296	Human	1	name
152036151	CV1604401	single nucleotide variant	NM_001558.4(IL10RA):c.1203T>C (p.Ser401=)	Inflammatory bowel disease 28 [RCV002087238]	likely benign	11	117999107	117999107	Human	1	name
152132588	CV1604803	single nucleotide variant	NM_001558.4(IL10RA):c.1701C>T (p.Thr567=)	Inflammatory bowel disease 28 [RCV002099688]	likely benign	11	117999605	117999605	Human	1	name
152113382	CV1623864	single nucleotide variant	NM_001558.4(IL10RA):c.1689A>C (p.Ser563=)	Inflammatory bowel disease 28 [RCV002134777]	likely benign	11	117999593	117999593	Human	1	name
152085428	CV1633490	single nucleotide variant	NM_001558.4(IL10RA):c.1704G>A (p.Leu568=)	Inflammatory bowel disease 28 [RCV002113319]	likely benign	11	117999608	117999608	Human	1	name
153303388	CV1686203	single nucleotide variant	NM_000628.5(IL10RB):c.130G>A (p.Ala44Thr)	not provided [RCV002261636]	uncertain significance	21	33268474	33268474	Human		name
155698884	CV1777365	single nucleotide variant	NM_000628.5(IL10RB):c.284A>T (p.Asp95Val)	Inflammatory bowel disease 25 [RCV002295489]	uncertain significance	21	33276706	33276706	Human	1	name
156376327	CV1868940	single nucleotide variant	NM_001558.4(IL10RA):c.1095C>T (p.Ser365=)	Inflammatory bowel disease 28 [RCV003066762]	likely benign	11	117998999	117998999	Human	1	name
156405794	CV1884621	single nucleotide variant	NM_001558.4(IL10RA):c.1734G>A (p.Glu578=)	Inflammatory bowel disease 28 [RCV003070135]	likely benign	11	117999638	117999638	Human	1	name
156442706	CV1948809	single nucleotide variant	NM_001558.4(IL10RA):c.1296G>A (p.Val432=)	Inflammatory bowel disease 28 [RCV003113054]	likely benign	11	117999200	117999200	Human	1	name
156415972	CV1983845	single nucleotide variant	NM_001558.4(IL10RA):c.155C>G (p.Ser52Cys)	Inflammatory bowel disease 28 [RCV002609932]	uncertain significance	11	117988469	117988469	Human	1	name
156082525	CV2012058	single nucleotide variant	NM_001558.4(IL10RA):c.1149A>G (p.Thr383=)	Inflammatory bowel disease 28 [RCV002706035]	likely benign	11	117999053	117999053	Human	1	name
156309941	CV2031475	single nucleotide variant	NM_000628.5(IL10RB):c.203A>T (p.Asn68Ile)	Inflammatory bowel disease 25 [RCV002716474]	uncertain significance	21	33276625	33276625	Human	1	name
156159397	CV2033746	single nucleotide variant	NM_001558.4(IL10RA):c.150T>G (p.Asn50Lys)	Inflammatory bowel disease 28 [RCV002741489]	uncertain significance	11	117988464	117988464	Human	1	name
156012426	CV2035695	single nucleotide variant	NM_001558.4(IL10RA):c.1551C>T (p.Asn517=)	Inflammatory bowel disease 28 [RCV002795171]	likely benign	11	117999455	117999455	Human	1	name
156287773	CV2058194	single nucleotide variant	NM_001558.4(IL10RA):c.284G>T (p.Gly95Val)	Inflammatory bowel disease 28 [RCV002833074]	uncertain significance	11	117989537	117989537	Human	1	name
156034646	CV2059335	single nucleotide variant	NM_001558.4(IL10RA):c.1404C>T (p.Pro468=)	Inflammatory bowel disease 28 [RCV002796200]	likely benign	11	117999308	117999308	Human	1	name
156110588	CV2082108	single nucleotide variant	NM_001558.4(IL10RA):c.1338C>T (p.Tyr446=)	Inflammatory bowel disease 28 [RCV002848435]	likely benign	11	117999242	117999242	Human	1	name
156107699	CV2096515	single nucleotide variant	NM_001558.4(IL10RA):c.1248A>G (p.Thr416=)	Inflammatory bowel disease 28 [RCV002913649]	likely benign	11	117999152	117999152	Human	1	name
156203227	CV2110147	single nucleotide variant	NM_000628.5(IL10RB):c.179G>C (p.Arg60Thr)	Inflammatory bowel disease 25 [RCV002957458]	uncertain significance	21	33276601	33276601	Human	1	name
156021567	CV2111071	single nucleotide variant	NM_001558.4(IL10RA):c.140C>G (p.Pro47Arg)	Inflammatory bowel disease 28 [RCV002909639]	uncertain significance	11	117988454	117988454	Human	1	name
156382184	CV2118103	single nucleotide variant	NM_001558.4(IL10RA):c.1110C>T (p.Ser370=)	Inflammatory bowel disease 28 [RCV002943223]	likely benign	11	117999014	117999014	Human	1	name
156357059	CV2126141	single nucleotide variant	NM_000628.5(IL10RB):c.116A>G (p.Gln39Arg)	Inflammatory bowel disease 25 [RCV002966735]	uncertain significance	21	33268460	33268460	Human	1	name
156041955	CV2143500	single nucleotide variant	NM_001558.4(IL10RA):c.187A>G (p.Arg63Gly)	Inborn genetic diseases [RCV003009002]\|Inflammatory bowel disease 28 [RCV002999558]	uncertain significance	11	117988501	117988501	Human	2	name
156165197	CV2169564	single nucleotide variant	NM_001558.4(IL10RA):c.1047A>C (p.Gly349=)	Inflammatory bowel disease 28 [RCV003023339]	likely benign	11	117998951	117998951	Human	1	name
11578487	CV269232	single nucleotide variant	NM_001558.4(IL10RA):c.170A>G (p.Tyr57Cys)	Inflammatory bowel disease 28 [RCV000804486]\|not provided [RCV000282398]	likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	11	117988484	117988484	Human	1	name
405867473	CV2831805	deletion	NM_000628.5(IL10RB):c.25_43del (p.Leu9fs)	Inflammatory bowel disease 25 [RCV004560170]	likely pathogenic	21	33266485	33266503	Human	1	name
405007285	CV2882075	single nucleotide variant	NM_001558.4(IL10RA):c.1431C>T (p.Phe477=)	Inflammatory bowel disease 28 [RCV003526912]	likely benign	11	117999335	117999335	Human	1	name
405009443	CV2887056	single nucleotide variant	NM_001558.4(IL10RA):c.1272C>T (p.His424=)	Inflammatory bowel disease 28 [RCV003527103]	likely benign	11	117999176	117999176	Human	1	name
405178829	CV2946054	single nucleotide variant	NM_001558.4(IL10RA):c.1173G>A (p.Val391=)	Inflammatory bowel disease 28 [RCV003639411]	likely benign	11	117999077	117999077	Human	1	name
405181634	CV2969014	single nucleotide variant	NM_001558.4(IL10RA):c.1671C>A (p.Leu557=)	Inflammatory bowel disease 28 [RCV003639719]	likely benign	11	117999575	117999575	Human	1	name
8564473	CV29854	single nucleotide variant	NM_001558.4(IL10RA):c.251C>T (p.Thr84Ile)	Inflammatory bowel disease 28 [RCV000015938]	pathogenic	11	117989504	117989504	Human	1	name
405177680	CV3071586	single nucleotide variant	NM_001558.4(IL10RA):c.1446T>G (p.Val482=)	Inflammatory bowel disease 28 [RCV003639288]	likely benign	11	117999350	117999350	Human	1	name
405102424	CV3119427	single nucleotide variant	NM_001558.4(IL10RA):c.1113G>A (p.Gly371=)	Inflammatory bowel disease 28 [RCV003811688]	likely benign	11	117999017	117999017	Human	1	name
11601199	CV312439	single nucleotide variant	NM_001558.4(IL10RA):c.1281C>T (p.Pro427=)	Inflammatory bowel disease 28 [RCV000280203]	uncertain significance	11	117999185	117999185	Human	1	name
405094463	CV3164229	single nucleotide variant	NM_001558.4(IL10RA):c.1635T>G (p.Leu545=)	Inflammatory bowel disease 28 [RCV003852544]	likely benign	11	117999539	117999539	Human	1	name
402517164	CV3179026	single nucleotide variant	NM_001558.4(IL10RA):c.1239T>A (p.Ala413=)	Inflammatory bowel disease 28 [RCV003879459]	likely benign	11	117999143	117999143	Human	1	name
11610394	CV318324	single nucleotide variant	NM_001558.4(IL10RA):c.181C>G (p.Leu61Val)	Inflammatory bowel disease 28 [RCV000541829]\|not provided [RCV004703590]	benign\|likely benign	11	117988495	117988495	Human	1	name
11606728	CV318359	single nucleotide variant	NM_001558.4(IL10RA):c.1323G>A (p.Val441=)	Inflammatory bowel disease 28 [RCV000335288]	conflicting interpretations of pathogenicity\|uncertain significance	11	117999227	117999227	Human	1	name
8600371	CV31962	single nucleotide variant	NM_000628.5(IL10RB):c.139A>G (p.Lys47Glu)	Hepatitis B virus, susceptibility to [RCV000018431]\|Inflammatory bowel disease 25 [RCV000392488]\|not provided [RCV004716909]\|not specified [RCV000455211]	risk factor\|benign	21	33268483	33268483	Human	7	name
11657329	CV325211	single nucleotide variant	NM_001558.4(IL10RA):c.295A>T (p.Arg99Ter)	Inflammatory bowel disease 28 [RCV000340619]	uncertain significance	11	117989548	117989548	Human		name
407479556	CV3440955	single nucleotide variant	NM_000628.5(IL10RB):c.164A>G (p.Gln55Arg)	Inborn genetic diseases [RCV004627919]	uncertain significance	21	33268508	33268508	Human	1	name
597699703	CV3690119	single nucleotide variant	NM_001558.4(IL10RA):c.212C>T (p.Ser71Phe)	Inborn genetic diseases [RCV004987792]	uncertain significance	11	117989465	117989465	Human	1	name
597830210	CV3746630	single nucleotide variant	NM_001558.4(IL10RA):c.1206C>T (p.Gly402=)	Inflammatory bowel disease 28 [RCV005061916]	likely benign	11	117999110	117999110	Human	1	name
597919893	CV3781177	single nucleotide variant	NM_001558.4(IL10RA):c.1194G>A (p.Gln398=)	Inflammatory bowel disease 28 [RCV005130059]	likely benign	11	117999098	117999098	Human	1	name
597972042	CV3794097	single nucleotide variant	NM_001558.4(IL10RA):c.1281C>A (p.Pro427=)	Inflammatory bowel disease 28 [RCV005142463]	likely benign	11	117999185	117999185	Human	1	name
597959746	CV3797635	single nucleotide variant	NM_000628.5(IL10RB):c.168C>G (p.Tyr56Ter)	Inflammatory bowel disease 25 [RCV005138322]	pathogenic	21	33268512	33268512	Human	1	name
597871363	CV3805994	single nucleotide variant	NM_001558.4(IL10RA):c.1441C>T (p.Leu481=)	Inflammatory bowel disease 28 [RCV005148404]	likely benign	11	117999345	117999345	Human	1	name
597960567	CV3811925	single nucleotide variant	NM_001558.4(IL10RA):c.1419T>G (p.Leu473=)	Inflammatory bowel disease 28 [RCV005163578]	likely benign	11	117999323	117999323	Human	1	name
597846158	CV3827929	single nucleotide variant	NM_001558.4(IL10RA):c.1263C>T (p.Ala421=)	Inflammatory bowel disease 28 [RCV005173004]	likely benign	11	117999167	117999167	Human	1	name
597917233	CV3861329	single nucleotide variant	NM_001558.4(IL10RA):c.1416C>G (p.Gly472=)	Inflammatory bowel disease 28 [RCV005204486]	likely benign	11	117999320	117999320	Human	1	name
13472010	CV460914	single nucleotide variant	NM_001558.4(IL10RA):c.136A>G (p.Thr46Ala)	Inflammatory bowel disease 28 [RCV000524699]\|not provided [RCV001701041]	benign\|likely benign	11	117988450	117988450	Human	1	name
13620000	CV525921	single nucleotide variant	NM_001558.4(IL10RA):c.1041G>A (p.Thr347=)	Inflammatory bowel disease 28 [RCV000647211]\|not provided [RCV004707396]	benign	11	117998945	117998945	Human	1	name
13620002	CV526417	single nucleotide variant	NM_001558.4(IL10RA):c.1158C>G (p.Thr386=)	Inflammatory bowel disease 28 [RCV000647213]\|not provided [RCV002060758]	benign\|likely benign	11	117999062	117999062	Human	1	name
13619997	CV526420	single nucleotide variant	NM_001558.4(IL10RA):c.1539G>A (p.Thr513=)	Inborn genetic diseases [RCV004985039]\|Inflammatory bowel disease 28 [RCV000647208]	likely benign\|conflicting interpretations of pathogenicity	11	117999443	117999443	Human	2	name
14727560	CV639723	single nucleotide variant	NM_001558.4(IL10RA):c.161G>C (p.Ser54Thr)	Inflammatory bowel disease 28 [RCV000799697]	uncertain significance	11	117988475	117988475	Human	1	name
15151515	CV712626	single nucleotide variant	NM_001558.4(IL10RA):c.1401G>A (p.Ser467=)	Inflammatory bowel disease 28 [RCV000968155]	benign\|conflicting interpretations of pathogenicity	11	117999305	117999305	Human	1	name
15185097	CV737750	single nucleotide variant	NM_001558.4(IL10RA):c.172G>A (p.Glu58Lys)	Inflammatory bowel disease 28 [RCV000908434]\|not provided [RCV004704305]	likely benign	11	117988486	117988486	Human	1	name
15108712	CV757750	single nucleotide variant	NM_000628.5(IL10RB):c.215C>T (p.Thr72Met)	Inflammatory bowel disease 25 [RCV000916193]	likely benign\|conflicting interpretations of pathogenicity	21	33276637	33276637	Human	1	name
26913688	CV838008	single nucleotide variant	NM_001558.4(IL10RA):c.114T>A (p.Phe38Leu)	Inflammatory bowel disease 28 [RCV001036342]	uncertain significance	11	117988428	117988428	Human	1	name
26919395	CV838009	single nucleotide variant	NM_001558.4(IL10RA):c.289C>T (p.Arg97Trp)	Inflammatory bowel disease 28 [RCV001045484]	uncertain significance	11	117989542	117989542	Human	1	name
26906852	CV848722	single nucleotide variant	NM_000628.5(IL10RB):c.120G>A (p.Trp40Ter)	Inflammatory bowel disease 25 [RCV001037664]	pathogenic	21	33268464	33268464	Human	1	name
26888706	CV848723	single nucleotide variant	NM_000628.5(IL10RB):c.157A>C (p.Thr53Pro)	Inflammatory bowel disease 25 [RCV001045365]	uncertain significance	21	33268501	33268501	Human	1	name
28907838	CV867073	single nucleotide variant	NM_001558.4(IL10RA):c.1707C>T (p.Pro569=)	Inflammatory bowel disease 28 [RCV001107440]	uncertain significance	11	117999611	117999611	Human	1	name
126760496	CV994333	single nucleotide variant	NM_001558.4(IL10RA):c.274C>T (p.His92Tyr)	Inflammatory bowel disease 28 [RCV001299810]	uncertain significance	11	117989527	117989527	Human	1	name
126757404	CV1009517	single nucleotide variant	NM_001558.4(IL10RA):c.530A>G (p.Asn177Ser)	Inflammatory bowel disease 28 [RCV001317481]	uncertain significance	11	117993403	117993403	Human	1	name
126749849	CV1009518	single nucleotide variant	NM_001558.4(IL10RA):c.910G>A (p.Val304Met)	Inflammatory bowel disease 28 [RCV001326615]	uncertain significance	11	117998814	117998814	Human	1	name
126755180	CV1014317	single nucleotide variant	NM_000628.5(IL10RB):c.652G>A (p.Val218Ile)	Inflammatory bowel disease 25 [RCV001316881]	uncertain significance	21	33288109	33288109	Human	1	name
126742663	CV1018733	single nucleotide variant	NM_000628.5(IL10RB):c.298T>G (p.Trp100Gly)	Inflammatory bowel disease 25 [RCV001330006]	uncertain significance	21	33276720	33276720	Human	1	name
126733369	CV1034884	single nucleotide variant	NM_000628.5(IL10RB):c.511C>A (p.Pro171Thr)	Inflammatory bowel disease 25 [RCV001349768]	uncertain significance	21	33283106	33283106	Human	1	name
126752072	CV1034885	single nucleotide variant	NM_000628.5(IL10RB):c.593G>A (p.Arg198Gln)	Inborn genetic diseases [RCV002547562]\|Inflammatory bowel disease 25 [RCV001352551]	uncertain significance	21	33283188	33283188	Human	2	name
126768838	CV1034887	single nucleotide variant	NM_000628.5(IL10RB):c.970C>T (p.Gln324Ter)	Inflammatory bowel disease 25 [RCV001343581]	uncertain significance	21	33296349	33296349	Human	1	name
126912005	CV1047048	single nucleotide variant	NM_001558.4(IL10RA):c.538T>G (p.Phe180Val)	Inflammatory bowel disease 28 [RCV001369505]	uncertain significance	11	117993999	117993999	Human	1	name
126918426	CV1051862	single nucleotide variant	NM_000628.5(IL10RB):c.833T>G (p.Leu278Arg)	Inflammatory bowel disease 25 [RCV001361713]	uncertain significance	21	33296212	33296212	Human	1	name
126917277	CV1051863	single nucleotide variant	NM_000628.5(IL10RB):c.857C>T (p.Ser286Leu)	Inflammatory bowel disease 25 [RCV001361074]\|not provided [RCV004692630]	uncertain significance	21	33296236	33296236	Human	1	name
127262484	CV1062241	single nucleotide variant	NM_001558.4(IL10RA):c.756C>A (p.Tyr252Ter)	Inflammatory bowel disease 28 [RCV001387734]	pathogenic	11	117995656	117995656	Human	1	name
151821862	CV1355049	single nucleotide variant	NM_001558.4(IL10RA):c.524C>T (p.Pro175Leu)	Inborn genetic diseases [RCV004043025]\|Inflammatory bowel disease 28 [RCV001934221]	uncertain significance	11	117993397	117993397	Human	2	name
151762493	CV1372044	single nucleotide variant	NM_001558.4(IL10RA):c.975G>C (p.Lys325Asn)	Inborn genetic diseases [RCV002562855]\|Inflammatory bowel disease 28 [RCV001987441]	uncertain significance	11	117998879	117998879	Human	2	name
151781255	CV1381632	single nucleotide variant	NM_000628.5(IL10RB):c.421G>A (p.Glu141Lys)	Inflammatory bowel disease 25 [RCV001883973]	uncertain significance	21	33279841	33279841	Human	1	name
151775398	CV1383596	single nucleotide variant	NM_000628.5(IL10RB):c.785T>G (p.Leu262Arg)	Inflammatory bowel disease 25 [RCV001874270]	uncertain significance	21	33288242	33288242	Human	1	name
151875568	CV1397151	single nucleotide variant	NM_001558.4(IL10RA):c.515G>A (p.Arg172His)	Inflammatory bowel disease 28 [RCV001940349]	uncertain significance	11	117993388	117993388	Human	1	name
151716171	CV1401040	single nucleotide variant	NM_000628.5(IL10RB):c.386T>G (p.Met129Arg)	Inflammatory bowel disease 25 [RCV002022762]	uncertain significance	21	33279806	33279806	Human	1	name
151799334	CV1412524	single nucleotide variant	NM_000628.5(IL10RB):c.641A>C (p.His214Pro)	Inflammatory bowel disease 25 [RCV001919632]	uncertain significance	21	33283236	33283236	Human	1	name
151805302	CV1429873	single nucleotide variant	NM_001558.4(IL10RA):c.769C>T (p.Gln257Ter)	Inflammatory bowel disease 28 [RCV001974279]	pathogenic\|likely pathogenic	11	117995669	117995669	Human	1	name
151725386	CV1433242	single nucleotide variant	NM_001558.4(IL10RA):c.416T>A (p.Ile139Asn)	Inflammatory bowel disease 28 [RCV001983617]	uncertain significance	11	117993289	117993289	Human	1	name
151667547	CV1448879	single nucleotide variant	NM_000628.5(IL10RB):c.682A>T (p.Met228Leu)	Inflammatory bowel disease 25 [RCV001990439]	uncertain significance	21	33288139	33288139	Human	1	name
151800696	CV1450295	single nucleotide variant	NM_000628.5(IL10RB):c.389G>A (p.Arg130His)	Inflammatory bowel disease 25 [RCV001922702]	uncertain significance	21	33279809	33279809	Human	1	name
151768719	CV1450841	single nucleotide variant	NM_001558.4(IL10RA):c.896A>T (p.Glu299Val)	Inflammatory bowel disease 28 [RCV001929308]	uncertain significance	11	117998800	117998800	Human	1	name
151786248	CV1456237	single nucleotide variant	NM_001558.4(IL10RA):c.922C>A (p.Leu308Met)	Inflammatory bowel disease 28 [RCV002046638]	uncertain significance	11	117998826	117998826	Human	1	name
151714060	CV1465491	single nucleotide variant	NM_000628.5(IL10RB):c.302T>C (p.Val101Ala)	Inflammatory bowel disease 25 [RCV002014146]	uncertain significance	21	33276724	33276724	Human	1	name
151889099	CV1468569	single nucleotide variant	NM_001558.4(IL10RA):c.517A>G (p.Lys173Glu)	Inflammatory bowel disease 28 [RCV002001222]	uncertain significance	11	117993390	117993390	Human	1	name
151889136	CV1468576	single nucleotide variant	NM_001558.4(IL10RA):c.426G>C (p.Lys142Asn)	Inflammatory bowel disease 28 [RCV002001229]	uncertain significance	11	117993299	117993299	Human	1	name
151773431	CV1470080	single nucleotide variant	NM_000628.5(IL10RB):c.311C>T (p.Thr104Ile)	Inflammatory bowel disease 25 [RCV001871067]	uncertain significance	21	33276733	33276733	Human	1	name
151778124	CV1470952	single nucleotide variant	NM_001558.4(IL10RA):c.851G>A (p.Arg284His)	Inflammatory bowel disease 28 [RCV001971824]	uncertain significance	11	117998755	117998755	Human	1	name
151833850	CV1479159	single nucleotide variant	NM_001558.4(IL10RA):c.697G>T (p.Val233Leu)	Inflammatory bowel disease 28 [RCV002050991]	uncertain significance	11	117995597	117995597	Human	1	name
151813952	CV1494716	single nucleotide variant	NM_001558.4(IL10RA):c.873C>G (p.Asp291Glu)	Inflammatory bowel disease 28 [RCV001954098]	uncertain significance	11	117998777	117998777	Human	1	name
151848047	CV1502521	single nucleotide variant	NM_001558.4(IL10RA):c.746C>A (p.Ala249Asp)	Inflammatory bowel disease 28 [RCV001882227]	uncertain significance	11	117995646	117995646	Human	1	name
151828345	CV1507798	single nucleotide variant	NM_000628.5(IL10RB):c.498G>C (p.Lys166Asn)	Inflammatory bowel disease 25 [RCV001978407]	uncertain significance	21	33279918	33279918	Human	1	name
151716637	CV1509108	single nucleotide variant	NM_000628.5(IL10RB):c.673G>A (p.Val225Ile)	Inborn genetic diseases [RCV002548911]\|Inflammatory bowel disease 25 [RCV002024067]	likely benign\|uncertain significance	21	33288130	33288130	Human	2	name
151832041	CV1512106	single nucleotide variant	NM_000628.5(IL10RB):c.641A>G (p.His214Arg)	Inflammatory bowel disease 25 [RCV001986209]	uncertain significance	21	33283236	33283236	Human	1	name
152145934	CV1631312	single nucleotide variant	NM_000628.5(IL10RB):c.388C>T (p.Arg130Cys)	Inflammatory bowel disease 25 [RCV002157428]	likely benign	21	33279808	33279808	Human	1	name
155749575	CV1771779	single nucleotide variant	NM_001558.4(IL10RA):c.742G>A (p.Gly248Arg)	Inflammatory bowel disease 28 [RCV002304793]	uncertain significance	11	117995642	117995642	Human	1	name
156066468	CV1874384	single nucleotide variant	NM_001558.4(IL10RA):c.470A>G (p.Tyr157Cys)	Inflammatory bowel disease 28 [RCV003037432]	pathogenic	11	117993343	117993343	Human	1	name
155940130	CV1913607	single nucleotide variant	NM_000628.5(IL10RB):c.568C>G (p.Gln190Glu)	Inflammatory bowel disease 25 [RCV002615575]	uncertain significance	21	33283163	33283163	Human	1	name
156290278	CV1926472	single nucleotide variant	NM_000628.5(IL10RB):c.584T>C (p.Leu195Pro)	Inflammatory bowel disease 25 [RCV002628784]	uncertain significance	21	33283179	33283179	Human	1	name
156176258	CV1927682	single nucleotide variant	NM_001558.4(IL10RA):c.782G>A (p.Arg261Gln)	Inflammatory bowel disease 28 [RCV002624885]	uncertain significance	11	117995682	117995682	Human	1	name
10052121	CV194358	single nucleotide variant	NM_001558.4(IL10RA):c.475A>G (p.Ser159Gly)	Inflammatory bowel disease 28 [RCV000605669]\|not provided [RCV004706616]\|not specified [RCV000178165]	benign\|likely benign	11	117993348	117993348	Human	5	name
156449193	CV1944451	single nucleotide variant	NM_001558.4(IL10RA):c.703A>G (p.Asn235Asp)	Inflammatory bowel disease 28 [RCV003121306]	uncertain significance	11	117995603	117995603	Human	1	name
156339037	CV1973966	single nucleotide variant	NM_001558.4(IL10RA):c.592G>A (p.Val198Met)	Inflammatory bowel disease 28 [RCV002601181]	uncertain significance	11	117994053	117994053	Human	1	name
156111711	CV1988810	single nucleotide variant	NM_001558.4(IL10RA):c.846C>A (p.Ser282Arg)	Inflammatory bowel disease 28 [RCV002622604]	uncertain significance	11	117998750	117998750	Human	1	name
156258103	CV1996839	single nucleotide variant	NM_000628.5(IL10RB):c.343C>A (p.Pro115Thr)	Inflammatory bowel disease 25 [RCV002646119]	uncertain significance	21	33279763	33279763	Human	1	name
156220662	CV2015484	single nucleotide variant	NM_001558.4(IL10RA):c.688T>C (p.Tyr230His)	Inflammatory bowel disease 28 [RCV002700993]	uncertain significance	11	117994149	117994149	Human	1	name
156371835	CV2031189	single nucleotide variant	NM_001558.4(IL10RA):c.736C>T (p.Leu246Phe)	Inflammatory bowel disease 28 [RCV002721577]	uncertain significance	11	117995636	117995636	Human	1	name
156324458	CV2032285	single nucleotide variant	NM_000628.5(IL10RB):c.511C>T (p.Pro171Ser)	Inborn genetic diseases [RCV004983103]\|Inflammatory bowel disease 25 [RCV002717316]	uncertain significance	21	33283106	33283106	Human	2	name
155933035	CV2035186	single nucleotide variant	NM_000628.5(IL10RB):c.680T>A (p.Leu227His)	Inflammatory bowel disease 25 [RCV002751267]	uncertain significance	21	33288137	33288137	Human	1	name
156295261	CV2043538	single nucleotide variant	NM_001558.4(IL10RA):c.635G>A (p.Arg212Gln)	Inflammatory bowel disease 28 [RCV002770945]	uncertain significance	11	117994096	117994096	Human	1	name
156176928	CV2051207	single nucleotide variant	NM_000628.5(IL10RB):c.377C>T (p.Ser126Phe)	Inflammatory bowel disease 25 [RCV002802134]	uncertain significance	21	33279797	33279797	Human	1	name
156282561	CV2051399	single nucleotide variant	NM_001558.4(IL10RA):c.362A>T (p.Asp121Val)	Inflammatory bowel disease 28 [RCV002832891]	uncertain significance	11	117989615	117989615	Human	1	name
156076823	CV2053475	single nucleotide variant	NM_001558.4(IL10RA):c.307G>C (p.Val103Leu)	Inflammatory bowel disease 28 [RCV002823727]	uncertain significance	11	117989560	117989560	Human	1	name
156087336	CV2060619	single nucleotide variant	NM_000628.5(IL10RB):c.301G>C (p.Val101Leu)	Inflammatory bowel disease 25 [RCV002824057]	uncertain significance	21	33276723	33276723	Human	1	name
156314010	CV2063626	single nucleotide variant	NM_000628.5(IL10RB):c.791A>G (p.Gln264Arg)	Inflammatory bowel disease 25 [RCV002834288]	uncertain significance	21	33288248	33288248	Human	1	name
156210550	CV2074212	single nucleotide variant	NM_001558.4(IL10RA):c.452C>G (p.Ala151Gly)	Inflammatory bowel disease 28 [RCV002829280]	uncertain significance	11	117993325	117993325	Human	1	name
156310616	CV2082349	single nucleotide variant	NM_001558.4(IL10RA):c.494G>A (p.Arg165Gln)	Inflammatory bowel disease 28 [RCV002898692]	uncertain significance	11	117993367	117993367	Human	1	name
156066081	CV2092813	single nucleotide variant	NM_000628.5(IL10RB):c.823C>T (p.His275Tyr)	Inflammatory bowel disease 25 [RCV002886663]	uncertain significance	21	33296202	33296202	Human	1	name
156083303	CV2094925	single nucleotide variant	NM_000628.5(IL10RB):c.383A>T (p.His128Leu)	Inflammatory bowel disease 25 [RCV002912774]	uncertain significance	21	33279803	33279803	Human	1	name
156024591	CV2112283	single nucleotide variant	NM_000628.5(IL10RB):c.612G>T (p.Trp204Cys)	Inflammatory bowel disease 25 [RCV002909774]	uncertain significance	21	33283207	33283207	Human	1	name
156229328	CV2121964	single nucleotide variant	NM_001558.4(IL10RA):c.859C>G (p.Pro287Ala)	Inflammatory bowel disease 28 [RCV002958447]	uncertain significance	11	117998763	117998763	Human	1	name
156342714	CV2123881	single nucleotide variant	NM_000628.5(IL10RB):c.598A>G (p.Lys200Glu)	Inflammatory bowel disease 25 [RCV002938984]	uncertain significance	21	33283193	33283193	Human	1	name
155972405	CV2148720	single nucleotide variant	NM_000628.5(IL10RB):c.863A>T (p.Glu288Val)	Inflammatory bowel disease 25 [RCV003015998]	uncertain significance	21	33296242	33296242	Human	1	name
156308258	CV2153899	single nucleotide variant	NM_000628.5(IL10RB):c.833T>C (p.Leu278Pro)	Inflammatory bowel disease 25 [RCV003028432]	uncertain significance	21	33296212	33296212	Human	1	name
156061039	CV2155110	single nucleotide variant	NM_000628.5(IL10RB):c.971A>G (p.Gln324Arg)	Inflammatory bowel disease 25 [RCV003000204]	uncertain significance	21	33296350	33296350	Human	1	name
156317767	CV2161576	single nucleotide variant	NM_001558.4(IL10RA):c.874A>G (p.Thr292Ala)	Inflammatory bowel disease 28 [RCV003046406]	uncertain significance	11	117998778	117998778	Human	1	name
156164832	CV2169535	single nucleotide variant	NM_001558.4(IL10RA):c.887T>C (p.Leu296Pro)	Inflammatory bowel disease 28 [RCV003023327]	uncertain significance	11	117998791	117998791	Human	1	name
155994859	CV2171506	single nucleotide variant	NM_000628.5(IL10RB):c.466G>A (p.Val156Met)	Inflammatory bowel disease 25 [RCV003034498]	uncertain significance	21	33279886	33279886	Human	1	name
156333820	CV2172071	single nucleotide variant	NM_001558.4(IL10RA):c.687G>C (p.Gln229His)	Inflammatory bowel disease 28 [RCV003029915]	uncertain significance	11	117994148	117994148	Human	1	name
156263219	CV2189022	single nucleotide variant	NM_001558.4(IL10RA):c.646G>A (p.Gly216Arg)	Inflammatory bowel disease 28 [RCV003044191]	uncertain significance	11	117994107	117994107	Human	1	name
156264746	CV2329468	single nucleotide variant	NM_001558.4(IL10RA):c.991G>A (p.Glu331Lys)	Inborn genetic diseases [RCV002959969]	uncertain significance	11	117998895	117998895	Human	1	name
155937494	CV2373634	single nucleotide variant	NM_000628.5(IL10RB):c.385A>G (p.Met129Val)	Inborn genetic diseases [RCV002729692]	uncertain significance	21	33279805	33279805	Human	1	name
243058469	CV2404895	single nucleotide variant	NM_000628.5(IL10RB):c.787C>G (p.Pro263Ala)	Inflammatory bowel disease 25 [RCV003140444]	uncertain significance	21	33288244	33288244	Human	1	name
243058167	CV2405469	single nucleotide variant	NM_001558.4(IL10RA):c.799C>G (p.Pro267Ala)	Inflammatory bowel disease 28 [RCV003133698]	uncertain significance	11	117995699	117995699	Human	1	name
11525674	CV247051	single nucleotide variant	NM_001558.4(IL10RA):c.781C>T (p.Arg261Trp)	Inflammatory bowel disease 28 [RCV001087846]\|not provided [RCV000767103]\|not specified [RCV000238699]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	11	117995681	117995681	Human	1	name
329353096	CV2471469	single nucleotide variant	NM_001558.4(IL10RA):c.310G>A (p.Asp104Asn)	Inborn genetic diseases [RCV003201007]	uncertain significance	11	117989563	117989563	Human	1	name
329351374	CV2478025	single nucleotide variant	NM_000628.5(IL10RB):c.435G>A (p.Met145Ile)	Hepatitis B virus, susceptibility to [RCV003224691]	uncertain significance	21	33279855	33279855	Human	1	name
329954651	CV2670592	single nucleotide variant	NM_001558.4(IL10RA):c.419T>G (p.Leu140Arg)	not provided [RCV003235859]	uncertain significance	11	117993292	117993292	Human		name
401762838	CV2720097	single nucleotide variant	NM_001558.4(IL10RA):c.492C>G (p.Phe164Leu)	Inborn genetic diseases [RCV003300347]	uncertain significance	11	117993365	117993365	Human	1	name
11640791	CV274180	single nucleotide variant	NM_001558.4(IL10RA):c.721G>C (p.Ala241Pro)	not provided [RCV000345305]	uncertain significance	11	117995621	117995621	Human		name
401881686	CV2783922	single nucleotide variant	NM_000628.5(IL10RB):c.665T>C (p.Met222Thr)	Inborn genetic diseases [RCV003385443]	uncertain significance	21	33288122	33288122	Human	1	name
405867484	CV2831803	single nucleotide variant	NM_000628.5(IL10RB):c.300G>A (p.Trp100Ter)	Inflammatory bowel disease 25 [RCV004565062]	pathogenic	21	33276722	33276722	Human	1	name
405008600	CV2883184	single nucleotide variant	NM_001558.4(IL10RA):c.501T>G (p.Tyr167Ter)	Inflammatory bowel disease 28 [RCV003527027]	pathogenic	11	117993374	117993374	Human	1	name
405014740	CV2919415	single nucleotide variant	NM_001558.4(IL10RA):c.349C>T (p.Arg117Cys)	Inflammatory bowel disease 28 [RCV003527589]	pathogenic	11	117989602	117989602	Human	1	name
405180527	CV2952699	single nucleotide variant	NM_001558.4(IL10RA):c.464A>G (p.Asp155Gly)	Inflammatory bowel disease 28 [RCV003639587]	uncertain significance	11	117993337	117993337	Human	1	name
405180273	CV2959383	single nucleotide variant	NM_000628.5(IL10RB):c.691G>A (p.Val231Ile)	Inflammatory bowel disease 25 [RCV003639557]	uncertain significance	21	33288148	33288148	Human	1	name
8564472	CV29853	single nucleotide variant	NM_001558.4(IL10RA):c.421G>A (p.Gly141Arg)	Inflammatory bowel disease 28 [RCV000015937]	pathogenic	11	117993294	117993294	Human	1	name
405129912	CV3114958	single nucleotide variant	NM_001558.4(IL10RA):c.401T>C (p.Ile134Thr)	Inflammatory bowel disease 28 [RCV003815803]	uncertain significance	11	117993274	117993274	Human	1	name
11604706	CV318338	single nucleotide variant	NM_001558.4(IL10RA):c.670A>G (p.Ile224Val)	Inflammatory bowel disease 28 [RCV000312221]\|not provided [RCV001597052]	benign	11	117994131	117994131	Human	1	name
11609054	CV318353	single nucleotide variant	NM_001558.4(IL10RA):c.785G>A (p.Arg262His)	Inflammatory bowel disease 28 [RCV000363512]\|not provided [RCV001815308]	uncertain significance	11	117995685	117995685	Human	1	name
8600372	CV31963	single nucleotide variant	NM_000628.5(IL10RB):c.477G>A (p.Trp159Ter)	Inflammatory bowel disease 25 [RCV000018432]	pathogenic	21	33279897	33279897	Human	1	name
11625331	CV324471	single nucleotide variant	NM_001558.4(IL10RA):c.320G>A (p.Arg107Gln)	Inflammatory bowel disease 28 [RCV000689947]\|not provided [RCV001701942]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	11	117989573	117989573	Human	1	name
11614420	CV324478	single nucleotide variant	NM_001558.4(IL10RA):c.706G>A (p.Val236Ile)	Inflammatory bowel disease 28 [RCV000685802]\|not provided [RCV004692983]	uncertain significance	11	117995606	117995606	Human	1	name
405804282	CV3274799	single nucleotide variant	NM_001558.4(IL10RA):c.500A>T (p.Tyr167Phe)	Inborn genetic diseases [RCV004404919]	uncertain significance	11	117993373	117993373	Human	1	name
405804284	CV3274800	single nucleotide variant	NM_001558.4(IL10RA):c.656C>T (p.Ser219Phe)	Inborn genetic diseases [RCV004404920]	uncertain significance	11	117994117	117994117	Human	1	name
405804286	CV3274801	single nucleotide variant	NM_000628.5(IL10RB):c.571G>A (p.Val191Ile)	Inborn genetic diseases [RCV004404921]	uncertain significance	21	33283166	33283166	Human	1	name
11626013	CV336599	single nucleotide variant	NM_000628.5(IL10RB):c.727G>A (p.Ala243Thr)	Inflammatory bowel disease 25 [RCV000815248]\|not provided [RCV003480609]	uncertain significance	21	33288184	33288184	Human	1	name
407479560	CV3440956	single nucleotide variant	NM_000628.5(IL10RB):c.698T>C (p.Met233Thr)	Inborn genetic diseases [RCV004627920]	uncertain significance	21	33288155	33288155	Human	1	name
11630467	CV346304	single nucleotide variant	NM_000628.5(IL10RB):c.484G>A (p.Gly162Ser)	Inborn genetic diseases [RCV004021845]\|Inflammatory bowel disease 25 [RCV000811479]	uncertain significance	21	33279904	33279904	Human	2	name
408365277	CV3500715	single nucleotide variant	NM_001558.4(IL10RA):c.493C>T (p.Arg165Ter)	Inflammatory bowel disease 28 [RCV004720704]	likely pathogenic	11	117993366	117993366	Human	1	name
408394720	CV3522035	single nucleotide variant	NM_001558.4(IL10RA):c.637A>G (p.Ser213Gly)	Inflammatory bowel disease 28 [RCV004764828]	uncertain significance	11	117994098	117994098	Human	1	name
597699677	CV3690115	single nucleotide variant	NM_001558.4(IL10RA):c.815T>A (p.Phe272Tyr)	Inborn genetic diseases [RCV004987788]	uncertain significance	11	117998719	117998719	Human	1	name
597699696	CV3690118	single nucleotide variant	NM_001558.4(IL10RA):c.830C>T (p.Pro277Leu)	Inborn genetic diseases [RCV004987791]	uncertain significance	11	117998734	117998734	Human	1	name
597849177	CV3793057	single nucleotide variant	NM_001558.4(IL10RA):c.455C>T (p.Pro152Leu)	Inflammatory bowel disease 28 [RCV005145193]	uncertain significance	11	117993328	117993328	Human	1	name
597938497	CV3808257	single nucleotide variant	NM_000628.5(IL10RB):c.710C>T (p.Ala237Val)	Inflammatory bowel disease 25 [RCV005158445]	uncertain significance	21	33288167	33288167	Human	1	name
597902337	CV3845512	single nucleotide variant	NM_001558.4(IL10RA):c.679A>C (p.Thr227Pro)	Inflammatory bowel disease 28 [RCV005181322]	uncertain significance	11	117994140	117994140	Human	1	name
598207244	CV3975992	single nucleotide variant	NM_001558.4(IL10RA):c.426G>T (p.Lys142Asn)	Inborn genetic diseases [RCV005337942]	uncertain significance	11	117993299	117993299	Human	1	name
598179233	CV3975993	single nucleotide variant	NM_001558.4(IL10RA):c.695C>T (p.Thr232Ile)	Inborn genetic diseases [RCV005352118]	uncertain significance	11	117995595	117995595	Human	1	name
598207248	CV3975994	single nucleotide variant	NM_001558.4(IL10RA):c.452C>T (p.Ala151Val)	Inborn genetic diseases [RCV005337943]	uncertain significance	11	117993325	117993325	Human	1	name
598179241	CV3975996	single nucleotide variant	NM_000628.5(IL10RB):c.461A>T (p.Tyr154Phe)	Inborn genetic diseases [RCV005352120]	uncertain significance	21	33279881	33279881	Human	1	name
13487771	CV460942	single nucleotide variant	NM_001558.4(IL10RA):c.698T>G (p.Val233Gly)	Inflammatory bowel disease 28 [RCV001084894]\|not provided [RCV000598085]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	11	117995598	117995598	Human	1	name
13499764	CV461720	single nucleotide variant	NM_001558.4(IL10RA):c.751G>A (p.Ala251Thr)	Inflammatory bowel disease 28 [RCV000540015]	uncertain significance	11	117995651	117995651	Human	1	name
8570417	CV48029	single nucleotide variant	NM_001558.4(IL10RA):c.784C>T (p.Arg262Cys)	Inflammatory bowel disease 28 [RCV000032625]	pathogenic	11	117995684	117995684	Human	1	name
13515867	CV490830	single nucleotide variant	NM_001558.4(IL10RA):c.302G>A (p.Arg101Gln)	Inflammatory bowel disease 28 [RCV000694673]\|not provided [RCV000594822]	likely pathogenic\|uncertain significance	11	117989555	117989555	Human	1	name
13516457	CV491185	single nucleotide variant	NM_001558.4(IL10RA):c.536C>T (p.Thr179Met)	Inflammatory bowel disease 28 [RCV001060072]\|not provided [RCV000595547]	uncertain significance	11	117993409	117993409	Human	1	name
8604993	CV50339	single nucleotide variant	NM_000628.5(IL10RB):c.421G>T (p.Glu141Ter)	Inflammatory bowel disease 25 [RCV000034826]	pathogenic	21	33279841	33279841	Human	1	name
13532514	CV512480	single nucleotide variant	NM_000628.5(IL10RB):c.562T>G (p.Cys188Gly)	Inborn genetic diseases [RCV000624271]	uncertain significance	21	33283157	33283157	Human	1	name
13620005	CV526003	single nucleotide variant	NM_001558.4(IL10RA):c.697G>A (p.Val233Met)	Inflammatory bowel disease 28 [RCV000647215]\|not provided [RCV003411527]	benign	11	117995597	117995597	Human	1	name
13619990	CV526083	single nucleotide variant	NM_001558.4(IL10RA):c.884C>T (p.Pro295Leu)	Inflammatory bowel disease 28 [RCV000647202]\|not provided [RCV001726288]\|not specified [RCV000736104]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	11	117998788	117998788	Human	1	name
13618302	CV534375	single nucleotide variant	NM_000628.5(IL10RB):c.446A>G (p.Tyr149Cys)	Inborn genetic diseases [RCV003162933]\|Inflammatory bowel disease 25 [RCV000645972]	uncertain significance	21	33279866	33279866	Human	2	name
13618303	CV534379	single nucleotide variant	NM_000628.5(IL10RB):c.913G>A (p.Gly305Ser)	Inborn genetic diseases [RCV004025687]\|Inflammatory bowel disease 25 [RCV000645973]	likely benign\|uncertain significance	21	33296292	33296292	Human	2	name
13814742	CV570306	single nucleotide variant	NM_001558.4(IL10RA):c.574C>T (p.Leu192Phe)	Inflammatory bowel disease 28 [RCV000691088]	uncertain significance	11	117994035	117994035	Human	1	name
13810759	CV573064	single nucleotide variant	NM_000628.5(IL10RB):c.646G>A (p.Glu216Lys)	Hepatitis B virus, susceptibility to [RCV002507194]\|Inflammatory bowel disease 25 [RCV000688434]	uncertain significance	21	33283241	33283241	Human	2	name
13804306	CV573067	single nucleotide variant	NM_000628.5(IL10RB):c.742G>A (p.Val248Ile)	Inborn genetic diseases [RCV002533565]\|Inflammatory bowel disease 25 [RCV000699566]	likely benign\|uncertain significance	21	33288199	33288199	Human	2	name
13806283	CV573762	single nucleotide variant	NM_000628.5(IL10RB):c.911G>A (p.Ser304Asn)	Inborn genetic diseases [RCV003243266]\|Inflammatory bowel disease 25 [RCV000700506]	uncertain significance	21	33296290	33296290	Human	2	name
13807200	CV575152	single nucleotide variant	NM_000628.5(IL10RB):c.718G>A (p.Gly240Ser)	Inborn genetic diseases [RCV003362889]\|Inflammatory bowel disease 25 [RCV000686584]\|not provided [RCV003480766]	uncertain significance	21	33288175	33288175	Human	2	name
14688142	CV620670	single nucleotide variant	NM_000628.5(IL10RB):c.611G>A (p.Trp204Ter)	Inflammatory bowel disease 25 [RCV000778639]	pathogenic\|likely pathogenic	21	33283206	33283206	Human	1	name
14720230	CV639724	single nucleotide variant	NM_001558.4(IL10RA):c.407A>G (p.Asn136Ser)	Inflammatory bowel disease 28 [RCV000796542]	uncertain significance	11	117993280	117993280	Human	1	name
14744777	CV639725	single nucleotide variant	NM_001558.4(IL10RA):c.473A>G (p.Glu158Gly)	Inflammatory bowel disease 28 [RCV000824319]	uncertain significance	11	117993346	117993346	Human	1	name
14710961	CV639726	single nucleotide variant	NM_001558.4(IL10RA):c.514C>T (p.Arg172Cys)	Inborn genetic diseases [RCV002536957]\|Inflammatory bowel disease 28 [RCV000793296]	uncertain significance	11	117993387	117993387	Human	2	name
14735483	CV639728	single nucleotide variant	NM_001558.4(IL10RA):c.628G>A (p.Ala210Thr)	Inflammatory bowel disease 28 [RCV000803176]	uncertain significance	11	117994089	117994089	Human	1	name
14722134	CV639730	single nucleotide variant	NM_001558.4(IL10RA):c.883C>T (p.Pro295Ser)	Inborn genetic diseases [RCV002538176]\|Inflammatory bowel disease 28 [RCV000813776]\|not provided [RCV001702838]	likely benign\|uncertain significance	11	117998787	117998787	Human	2	name
14736016	CV648927	single nucleotide variant	NM_000628.5(IL10RB):c.328G>A (p.Asp110Asn)	Inborn genetic diseases [RCV002537447]\|Inflammatory bowel disease 25 [RCV000819820]	uncertain significance	21	33276750	33276750	Human	2	name
14705893	CV648928	single nucleotide variant	NM_000628.5(IL10RB):c.332C>G (p.Thr111Ser)	Inflammatory bowel disease 25 [RCV000808261]	uncertain significance	21	33279752	33279752	Human	1	name
14734770	CV648929	single nucleotide variant	NM_000628.5(IL10RB):c.650C>T (p.Thr217Met)	Inflammatory bowel disease 25 [RCV000819286]	uncertain significance	21	33288107	33288107	Human	1	name
14733793	CV648930	single nucleotide variant	NM_000628.5(IL10RB):c.707T>C (p.Leu236Pro)	Inflammatory bowel disease 25 [RCV000818855]	uncertain significance	21	33288164	33288164	Human	1	name
14716079	CV648931	single nucleotide variant	NM_000628.5(IL10RB):c.715C>A (p.Leu239Ile)	Inflammatory bowel disease 25 [RCV000795010]	uncertain significance	21	33288172	33288172	Human	1	name
14706278	CV648932	single nucleotide variant	NM_000628.5(IL10RB):c.738G>T (p.Trp246Cys)	Inborn genetic diseases [RCV004986621]\|Inflammatory bowel disease 25 [RCV000808391]	uncertain significance	21	33288195	33288195	Human	2	name
14702908	CV648933	single nucleotide variant	NM_000628.5(IL10RB):c.795C>A (p.His265Gln)	Inflammatory bowel disease 25 [RCV000807141]	uncertain significance	21	33288252	33288252	Human	1	name
14725686	CV648934	single nucleotide variant	NM_000628.5(IL10RB):c.889G>A (p.Val297Ile)	Inflammatory bowel disease 25 [RCV000798924]	uncertain significance	21	33296268	33296268	Human	1	name
14706771	CV648935	single nucleotide variant	NM_000628.5(IL10RB):c.949A>T (p.Thr317Ser)	Inflammatory bowel disease 25 [RCV000792099]	uncertain significance	21	33296328	33296328	Human	1	name
15200426	CV724210	single nucleotide variant	NM_001558.4(IL10RA):c.716T>C (p.Phe239Ser)	Inflammatory bowel disease 28 [RCV000890908]	benign\|likely benign	11	117995616	117995616	Human	1	name
21072284	CV791102	single nucleotide variant	NM_001558.4(IL10RA):c.787C>T (p.Arg263Ter)	Inflammatory bowel disease 28 [RCV000988744]	likely pathogenic	11	117995687	117995687	Human	1	name
21073220	CV792005	single nucleotide variant	NM_000628.5(IL10RB):c.476G>A (p.Trp159Ter)	Inflammatory bowel disease 25 [RCV000990344]	pathogenic	21	33279896	33279896	Human	1	name
25315128	CV818394	single nucleotide variant	NM_001558.4(IL10RA):c.634C>T (p.Arg212Ter)	Inflammatory bowel disease 28 [RCV001030032]	pathogenic	11	117994095	117994095	Human	1	name
26922265	CV838010	single nucleotide variant	NM_001558.4(IL10RA):c.457G>A (p.Ala153Thr)	Inborn genetic diseases [RCV004031616]\|Inflammatory bowel disease 28 [RCV001051836]	uncertain significance	11	117993330	117993330	Human	2	name
26918538	CV838011	single nucleotide variant	NM_001558.4(IL10RA):c.712A>G (p.Ile238Val)	Inflammatory bowel disease 28 [RCV001043892]	uncertain significance	11	117995612	117995612	Human	1	name
26889490	CV838012	single nucleotide variant	NM_001558.4(IL10RA):c.802A>G (p.Ser268Gly)	Inflammatory bowel disease 28 [RCV001058249]	uncertain significance	11	117995702	117995702	Human	1	name
26885832	CV838013	single nucleotide variant	NM_001558.4(IL10RA):c.818A>G (p.Lys273Arg)	Inflammatory bowel disease 28 [RCV001054214]	uncertain significance	11	117998722	117998722	Human	1	name
26887427	CV838014	single nucleotide variant	NM_001558.4(IL10RA):c.824C>T (p.Pro275Leu)	Inflammatory bowel disease 28 [RCV001056334]	uncertain significance	11	117998728	117998728	Human	1	name
26891804	CV848724	single nucleotide variant	NM_000628.5(IL10RB):c.575G>A (p.Arg192Gln)	Inflammatory bowel disease 25 [RCV001068406]	uncertain significance	21	33283170	33283170	Human	1	name
26885030	CV848725	single nucleotide variant	NM_000628.5(IL10RB):c.839T>C (p.Phe280Ser)	Inflammatory bowel disease 25 [RCV001065207]	uncertain significance	21	33296218	33296218	Human	1	name
26902031	CV848726	single nucleotide variant	NM_000628.5(IL10RB):c.953C>T (p.Pro318Leu)	Inborn genetic diseases [RCV004986736]\|Inflammatory bowel disease 25 [RCV001035851]\|not provided [RCV003480909]	likely benign\|uncertain significance	21	33296332	33296332	Human	2	name
28906555	CV867071	single nucleotide variant	NM_001558.4(IL10RA):c.313G>A (p.Gly105Ser)	Inflammatory bowel disease 28 [RCV001106718]	uncertain significance	11	117989566	117989566	Human	1	name
38478219	CV926132	single nucleotide variant	NM_001558.4(IL10RA):c.632C>T (p.Ser211Phe)	Inflammatory bowel disease 28 [RCV001216508]	uncertain significance	11	117994093	117994093	Human	1	name
38473237	CV929305	single nucleotide variant	NM_000628.5(IL10RB):c.367C>T (p.Leu123Phe)	Inflammatory bowel disease 25 [RCV001214334]	uncertain significance	21	33279787	33279787	Human	1	name
38472762	CV935401	single nucleotide variant	NM_001558.4(IL10RA):c.506T>C (p.Ile169Thr)	Inflammatory bowel disease 28 [RCV001214188]	pathogenic\|likely pathogenic\|uncertain significance	11	117993379	117993379	Human	1	name
38490011	CV935402	single nucleotide variant	NM_001558.4(IL10RA):c.580A>T (p.Thr194Ser)	Inflammatory bowel disease 28 [RCV001210458]	uncertain significance	11	117994041	117994041	Human	1	name
38477787	CV939084	single nucleotide variant	NM_000628.5(IL10RB):c.610T>C (p.Trp204Arg)	Inflammatory bowel disease 25 [RCV001205247]	uncertain significance	21	33283205	33283205	Human	1	name
38475579	CV939085	single nucleotide variant	NM_000628.5(IL10RB):c.689C>A (p.Ser230Ter)	Inflammatory bowel disease 25 [RCV001204314]	pathogenic	21	33288146	33288146	Human	1	name
38475348	CV939087	single nucleotide variant	NM_000628.5(IL10RB):c.946G>A (p.Gly316Arg)	Inborn genetic diseases [RCV004986939]\|Inflammatory bowel disease 25 [RCV001204237]\|not provided [RCV001509077]	likely benign\|uncertain significance	21	33296325	33296325	Human	2	name
38460488	CV947331	single nucleotide variant	NM_001558.4(IL10RA):c.943G>A (p.Gly315Ser)	Inflammatory bowel disease 28 [RCV001229360]	uncertain significance	11	117998847	117998847	Human	1	name
38457552	CV951210	single nucleotide variant	NM_000628.5(IL10RB):c.548C>G (p.Pro183Arg)	Inborn genetic diseases [RCV002563145]\|Inflammatory bowel disease 25 [RCV001228696]\|not provided [RCV004792826]	uncertain significance	21	33283143	33283143	Human	2	name
38495178	CV951211	single nucleotide variant	NM_000628.5(IL10RB):c.841T>G (p.Phe281Val)	Inflammatory bowel disease 25 [RCV001225552]	uncertain significance	21	33296220	33296220	Human	1	name
38468688	CV951212	single nucleotide variant	NM_000628.5(IL10RB):c.871G>A (p.Val291Ile)	Inflammatory bowel disease 25 [RCV001230671]	uncertain significance	21	33296250	33296250	Human	1	name
38493122	CV956394	single nucleotide variant	NM_001558.4(IL10RA):c.319C>T (p.Arg107Trp)	Inflammatory bowel disease 28 [RCV001240320]	uncertain significance	11	117989572	117989572	Human	1	name
38493333	CV956395	single nucleotide variant	NM_001558.4(IL10RA):c.788G>A (p.Arg263Gln)	Inborn genetic diseases [RCV004986995]\|Inflammatory bowel disease 28 [RCV001240623]	uncertain significance	11	117995688	117995688	Human	2	name
38491614	CV958942	single nucleotide variant	NM_000628.5(IL10RB):c.537A>C (p.Arg179Ser)	Inflammatory bowel disease 25 [RCV001239505]	uncertain significance	21	33283132	33283132	Human	1	name
38457861	CV958943	single nucleotide variant	NM_000628.5(IL10RB):c.917A>G (p.Lys306Arg)	Inflammatory bowel disease 25 [RCV001246181]	uncertain significance	21	33296296	33296296	Human	1	name
126739621	CV994334	single nucleotide variant	NM_001558.4(IL10RA):c.447G>T (p.Lys149Asn)	Inflammatory bowel disease 28 [RCV001305165]	uncertain significance	11	117993320	117993320	Human	1	name
126758323	CV994335	single nucleotide variant	NM_001558.4(IL10RA):c.670A>T (p.Ile224Phe)	Inflammatory bowel disease 28 [RCV001299151]	uncertain significance	11	117994131	117994131	Human	1	name
126752107	CV994336	single nucleotide variant	NM_001558.4(IL10RA):c.700A>G (p.Thr234Ala)	Inflammatory bowel disease 28 [RCV001307166]	uncertain significance	11	117995600	117995600	Human	1	name
126748664	CV994337	single nucleotide variant	NM_001558.4(IL10RA):c.734T>C (p.Leu245Pro)	Inborn genetic diseases [RCV004987052]\|Inflammatory bowel disease 28 [RCV001306479]	uncertain significance	11	117995634	117995634	Human	2	name
126757726	CV999165	single nucleotide variant	NM_000628.5(IL10RB):c.830C>T (p.Thr277Ile)	Inflammatory bowel disease 25 [RCV001308509]	uncertain significance	21	33296209	33296209	Human	1	name
126725898	CV999166	single nucleotide variant	NM_000628.5(IL10RB):c.862G>A (p.Glu288Lys)	Inflammatory bowel disease 25 [RCV001302720]	uncertain significance	21	33296241	33296241	Human	1	name
126727312	CV999167	single nucleotide variant	NM_000628.5(IL10RB):c.933C>A (p.Asp311Glu)	Inflammatory bowel disease 25 [RCV001303125]	uncertain significance	21	33296312	33296312	Human	1	name
126728147	CV1009519	single nucleotide variant	NM_001558.4(IL10RA):c.1019C>T (p.Pro340Leu)	Inflammatory bowel disease 28 [RCV001312446]\|not provided [RCV004793407]	uncertain significance	11	117998923	117998923	Human	1	name
126740075	CV1009520	single nucleotide variant	NM_001558.4(IL10RA):c.1247C>T (p.Thr416Ile)	Inflammatory bowel disease 28 [RCV001314329]	uncertain significance	11	117999151	117999151	Human	1	name
126737839	CV1009521	single nucleotide variant	NM_001558.4(IL10RA):c.1400C>T (p.Ser467Leu)	Inflammatory bowel disease 28 [RCV001324852]	uncertain significance	11	117999304	117999304	Human	1	name
126746410	CV1030077	single nucleotide variant	NM_001558.4(IL10RA):c.1002G>C (p.Gln334His)	Inflammatory bowel disease 28 [RCV001351518]	uncertain significance	11	117998906	117998906	Human	1	name
126774664	CV1030078	single nucleotide variant	NM_001558.4(IL10RA):c.1174G>A (p.Gly392Arg)	Inborn genetic diseases [RCV005340824]\|Inflammatory bowel disease 28 [RCV001347490]	uncertain significance	11	117999078	117999078	Human	2	name
126748559	CV1030079	single nucleotide variant	NM_001558.4(IL10RA):c.1537A>G (p.Thr513Ala)	Inflammatory bowel disease 28 [RCV001351883]	uncertain significance	11	117999441	117999441	Human	1	name
126766953	CV1030080	single nucleotide variant	NM_001558.4(IL10RA):c.1699A>C (p.Thr567Pro)	Inflammatory bowel disease 28 [RCV001342626]	uncertain significance	11	117999603	117999603	Human	1	name
126923942	CV1047049	single nucleotide variant	NM_001558.4(IL10RA):c.1247C>G (p.Thr416Arg)	Inflammatory bowel disease 28 [RCV001366439]	uncertain significance	11	117999151	117999151	Human	1	name
126919863	CV1047050	single nucleotide variant	NM_001558.4(IL10RA):c.1318G>T (p.Ala440Ser)	Inflammatory bowel disease 28 [RCV001373474]	uncertain significance	11	117999222	117999222	Human	1	name
126913354	CV1047051	single nucleotide variant	NM_001558.4(IL10RA):c.1321G>A (p.Val441Met)	Inborn genetic diseases [RCV002550097]\|Inflammatory bowel disease 28 [RCV001370072]	uncertain significance	11	117999225	117999225	Human	2	name
126909791	CV1047052	single nucleotide variant	NM_001558.4(IL10RA):c.1729A>T (p.Ser577Cys)	Inflammatory bowel disease 28 [RCV001368644]	uncertain significance	11	117999633	117999633	Human	1	name
127259412	CV1077894	single nucleotide variant	NM_001558.4(IL10RA):c.1415G>A (p.Gly472Asp)	Inflammatory bowel disease 28 [RCV001419792]	likely benign	11	117999319	117999319	Human	1	name
151796073	CV1352384	single nucleotide variant	NM_001558.4(IL10RA):c.1111G>A (p.Gly371Arg)	Inborn genetic diseases [RCV004988829]\|Inflammatory bowel disease 28 [RCV001876951]	uncertain significance	11	117999015	117999015	Human	2	name
151749548	CV1357156	single nucleotide variant	NM_001558.4(IL10RA):c.1624G>T (p.Ala542Ser)	Inflammatory bowel disease 28 [RCV001872114]	uncertain significance	11	117999528	117999528	Human	1	name
151722169	CV1361545	single nucleotide variant	NM_001558.4(IL10RA):c.1590C>G (p.Ser530Arg)	Inflammatory bowel disease 28 [RCV001945073]	uncertain significance	11	117999494	117999494	Human	1	name
151831430	CV1377909	single nucleotide variant	NM_001558.4(IL10RA):c.1534C>T (p.Pro512Ser)	Inflammatory bowel disease 28 [RCV002014347]	uncertain significance	11	117999438	117999438	Human	1	name
151759187	CV1391841	single nucleotide variant	NM_001558.4(IL10RA):c.1408A>G (p.Thr470Ala)	Inflammatory bowel disease 28 [RCV002044073]	uncertain significance	11	117999312	117999312	Human	1	name
151825388	CV1393720	single nucleotide variant	NM_001558.4(IL10RA):c.1495C>T (p.Gln499Ter)	Inflammatory bowel disease 28 [RCV002030292]	uncertain significance	11	117999399	117999399	Human	1	name
151822844	CV1424956	single nucleotide variant	NM_001558.4(IL10RA):c.1108A>T (p.Ser370Cys)	Inflammatory bowel disease 28 [RCV001919744]	uncertain significance	11	117999012	117999012	Human	1	name
151834188	CV1428954	single nucleotide variant	NM_001558.4(IL10RA):c.1166A>T (p.Gln389Leu)	Inflammatory bowel disease 28 [RCV001994011]	uncertain significance	11	117999070	117999070	Human	1	name
151862598	CV1448900	single nucleotide variant	NM_001558.4(IL10RA):c.1118G>T (p.Cys373Phe)	Inborn genetic diseases [RCV005343212]\|Inflammatory bowel disease 28 [RCV001959412]	uncertain significance	11	117999022	117999022	Human	2	name
151876639	CV1484415	single nucleotide variant	NM_001558.4(IL10RA):c.1253G>A (p.Gly418Asp)	Inflammatory bowel disease 28 [RCV001981985]	uncertain significance	11	117999157	117999157	Human	1	name
151858952	CV1486488	single nucleotide variant	NM_001558.4(IL10RA):c.1309G>A (p.Asp437Asn)	Inflammatory bowel disease 28 [RCV001883678]	uncertain significance	11	117999213	117999213	Human	1	name
151881192	CV1504119	single nucleotide variant	NM_001558.4(IL10RA):c.1369G>A (p.Ala457Thr)	Inflammatory bowel disease 28 [RCV002020189]	uncertain significance	11	117999273	117999273	Human	1	name
151757714	CV1510427	single nucleotide variant	NM_001558.4(IL10RA):c.1318G>A (p.Ala440Thr)	Inborn genetic diseases [RCV004043000]\|Inflammatory bowel disease 28 [RCV001948790]	uncertain significance	11	117999222	117999222	Human	2	name
151860947	CV1511065	single nucleotide variant	NM_001558.4(IL10RA):c.1139G>A (p.Ser380Asn)	Inflammatory bowel disease 28 [RCV001959218]	uncertain significance	11	117999043	117999043	Human	1	name
156446385	CV1937853	single nucleotide variant	NM_001558.4(IL10RA):c.1685A>T (p.Asn562Ile)	Inflammatory bowel disease 28 [RCV003117888]	uncertain significance	11	117999589	117999589	Human	1	name
156385870	CV1961232	single nucleotide variant	NM_001558.4(IL10RA):c.1091G>A (p.Ser364Asn)	Inflammatory bowel disease 28 [RCV002583477]	uncertain significance	11	117998995	117998995	Human	1	name
156409485	CV1961815	single nucleotide variant	NM_001558.4(IL10RA):c.1064T>A (p.Val355Glu)	Inborn genetic diseases [RCV002589007]\|Inflammatory bowel disease 28 [RCV002586834]	likely benign\|uncertain significance	11	117998968	117998968	Human	2	name
156411141	CV1976110	single nucleotide variant	NM_001558.4(IL10RA):c.1183A>G (p.Ser395Gly)	Inflammatory bowel disease 28 [RCV002587393]	uncertain significance	11	117999087	117999087	Human	1	name
156166469	CV1993270	single nucleotide variant	NM_001558.4(IL10RA):c.1594A>G (p.Ser532Gly)	Inflammatory bowel disease 28 [RCV002642591]	uncertain significance	11	117999498	117999498	Human	1	name
156350518	CV2001313	single nucleotide variant	NM_001558.4(IL10RA):c.1141C>T (p.Pro381Ser)	Inflammatory bowel disease 28 [RCV002675559]	uncertain significance	11	117999045	117999045	Human	1	name
155962601	CV2034001	single nucleotide variant	NM_001558.4(IL10RA):c.1270C>A (p.His424Asn)	Inflammatory bowel disease 28 [RCV002731247]	uncertain significance	11	117999174	117999174	Human	1	name
156129715	CV2037350	single nucleotide variant	NM_001558.4(IL10RA):c.1715C>G (p.Ser572Cys)	Inflammatory bowel disease 28 [RCV002800565]	uncertain significance	11	117999619	117999619	Human	1	name
156009242	CV2075413	single nucleotide variant	NM_001558.4(IL10RA):c.1567T>C (p.Trp523Arg)	Inflammatory bowel disease 28 [RCV002843782]	uncertain significance	11	117999471	117999471	Human	1	name
156095929	CV2110543	single nucleotide variant	NM_001558.4(IL10RA):c.1409C>G (p.Thr470Arg)	Inflammatory bowel disease 28 [RCV002926859]	uncertain significance	11	117999313	117999313	Human	1	name
155914343	CV2242685	single nucleotide variant	NM_001558.4(IL10RA):c.1035C>G (p.Asp345Glu)	Inborn genetic diseases [RCV002772048]	uncertain significance	11	117998939	117998939	Human	1	name
156262448	CV2287610	single nucleotide variant	NM_001558.4(IL10RA):c.1620C>A (p.Ser540Arg)	Inborn genetic diseases [RCV002855506]	uncertain significance	11	117999524	117999524	Human	1	name
156211367	CV2306152	single nucleotide variant	NM_001558.4(IL10RA):c.1025C>T (p.Pro342Leu)	Inborn genetic diseases [RCV002875483]	uncertain significance	11	117998929	117998929	Human	1	name
401864400	CV2773432	single nucleotide variant	NM_001558.4(IL10RA):c.1322T>C (p.Val441Ala)	Inborn genetic diseases [RCV003378811]	uncertain significance	11	117999226	117999226	Human	1	name
405178811	CV2945688	single nucleotide variant	NM_001558.4(IL10RA):c.1240G>A (p.Gly414Arg)	Inflammatory bowel disease 28 [RCV003639409]	uncertain significance	11	117999144	117999144	Human	1	name
405167185	CV3026421	single nucleotide variant	NM_001558.4(IL10RA):c.1093A>G (p.Ser365Gly)	Inflammatory bowel disease 28 [RCV003638167]	uncertain significance	11	117998997	117998997	Human	1	name
405091199	CV3167913	single nucleotide variant	NM_001558.4(IL10RA):c.1502C>T (p.Pro501Leu)	Inflammatory bowel disease 28 [RCV003852303]	uncertain significance	11	117999406	117999406	Human	1	name
402475713	CV3173681	single nucleotide variant	NM_001558.4(IL10RA):c.1324G>T (p.Ala442Ser)	Inflammatory bowel disease 28 [RCV003875219]	uncertain significance	11	117999228	117999228	Human	1	name
402469933	CV3174848	single nucleotide variant	NM_001558.4(IL10RA):c.1669C>T (p.Leu557Phe)	Inflammatory bowel disease 28 [RCV003873959]	uncertain significance	11	117999573	117999573	Human	1	name
11601580	CV318357	single nucleotide variant	NM_001558.4(IL10RA):c.1051A>G (p.Arg351Gly)	Inflammatory bowel disease 28 [RCV000283667]\|not provided [RCV001723887]\|not specified [RCV000455516]	benign	11	117998955	117998955	Human	1	name
11610280	CV318358	single nucleotide variant	NM_001558.4(IL10RA):c.1259C>T (p.Ser420Leu)	Inflammatory bowel disease 28 [RCV000535910]\|not provided [RCV002225580]	benign\|likely benign	11	117999163	117999163	Human	1	name
405804280	CV3274798	single nucleotide variant	NM_001558.4(IL10RA):c.1569G>T (p.Trp523Cys)	Inborn genetic diseases [RCV004404918]	uncertain significance	11	117999473	117999473	Human	1	name
407515509	CV3440952	single nucleotide variant	NM_001558.4(IL10RA):c.1619G>T (p.Ser540Ile)	Inborn genetic diseases [RCV004627916]	uncertain significance	11	117999523	117999523	Human	1	name
407515512	CV3440953	single nucleotide variant	NM_001558.4(IL10RA):c.1468C>G (p.Pro490Ala)	Inborn genetic diseases [RCV004627917]	uncertain significance	11	117999372	117999372	Human	1	name
408370054	CV3502985	single nucleotide variant	NM_001558.4(IL10RA):c.1649G>A (p.Cys550Tyr)	not provided [RCV004724106]	uncertain significance	11	117999553	117999553	Human		name
597699673	CV3690114	single nucleotide variant	NM_001558.4(IL10RA):c.1618A>G (p.Ser540Gly)	Inborn genetic diseases [RCV004987787]	uncertain significance	11	117999522	117999522	Human	1	name
597699711	CV3690120	single nucleotide variant	NM_001558.4(IL10RA):c.1706C>T (p.Pro569Leu)	Inborn genetic diseases [RCV004987793]	uncertain significance	11	117999610	117999610	Human	1	name
597699712	CV3690121	single nucleotide variant	NM_001558.4(IL10RA):c.1100G>A (p.Ser367Asn)	Inborn genetic diseases [RCV004987794]	uncertain significance	11	117999004	117999004	Human	1	name
597904107	CV3741594	single nucleotide variant	NM_001558.4(IL10RA):c.1531G>A (p.Ala511Thr)	Inflammatory bowel disease 28 [RCV005072565]	uncertain significance	11	117999435	117999435	Human	1	name
597889474	CV3788102	single nucleotide variant	NM_001558.4(IL10RA):c.1181A>G (p.Asn394Ser)	Inflammatory bowel disease 28 [RCV005125460]	uncertain significance	11	117999085	117999085	Human	1	name
13475062	CV460899	single nucleotide variant	NM_001558.4(IL10RA):c.1360G>A (p.Glu454Lys)	Inflammatory bowel disease 28 [RCV000548542]	benign\|likely benign	11	117999264	117999264	Human	1	name
13619992	CV525924	single nucleotide variant	NM_001558.4(IL10RA):c.1072G>A (p.Asp358Asn)	Inflammatory bowel disease 28 [RCV000647204]\|not provided [RCV001702705]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	11	117998976	117998976	Human	1	name
13619991	CV526004	single nucleotide variant	NM_001558.4(IL10RA):c.1234C>T (p.Arg412Trp)	Inflammatory bowel disease 28 [RCV000647203]	uncertain significance	11	117999138	117999138	Human	1	name
13619994	CV526086	single nucleotide variant	NM_001558.4(IL10RA):c.1235G>A (p.Arg412Gln)	Inflammatory bowel disease 28 [RCV000647205]\|not provided [RCV001700437]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	11	117999139	117999139	Human	1	name
13808711	CV567052	single nucleotide variant	NM_001558.4(IL10RA):c.1145G>C (p.Ser382Thr)	Inborn genetic diseases [RCV004629308]\|Inflammatory bowel disease 28 [RCV000701705]	uncertain significance	11	117999049	117999049	Human	2	name
13833098	CV584326	single nucleotide variant	NM_001558.4(IL10RA):c.1640C>T (p.Pro547Leu)	not provided [RCV000728254]	uncertain significance	11	117999544	117999544	Human		name
14729328	CV639731	single nucleotide variant	NM_001558.4(IL10RA):c.1169A>T (p.Gln390Leu)	Inflammatory bowel disease 28 [RCV000800437]	uncertain significance	11	117999073	117999073	Human	1	name
14735118	CV639732	single nucleotide variant	NM_001558.4(IL10RA):c.1432G>A (p.Gly478Arg)	Inflammatory bowel disease 28 [RCV000819447]	uncertain significance	11	117999336	117999336	Human	1	name
14710233	CV639733	single nucleotide variant	NM_001558.4(IL10RA):c.1538C>T (p.Thr513Met)	Inflammatory bowel disease 28 [RCV000809545]\|not provided [RCV003480852]	uncertain significance	11	117999442	117999442	Human	1	name
14705476	CV639734	single nucleotide variant	NM_001558.4(IL10RA):c.1631A>T (p.Asp544Val)	Inflammatory bowel disease 28 [RCV000791695]	uncertain significance	11	117999535	117999535	Human	1	name
14709038	CV639735	single nucleotide variant	NM_001558.4(IL10RA):c.1693C>A (p.Leu565Met)	Inflammatory bowel disease 28 [RCV000792750]	uncertain significance	11	117999597	117999597	Human	1	name
15157687	CV737752	single nucleotide variant	NM_001558.4(IL10RA):c.1283C>T (p.Pro428Leu)	Inflammatory bowel disease 28 [RCV001106802]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	11	117999187	117999187	Human	1	name
26884744	CV838016	single nucleotide variant	NM_001558.4(IL10RA):c.1165C>A (p.Gln389Lys)	Inborn genetic diseases [RCV005338538]\|Inflammatory bowel disease 28 [RCV001052475]	uncertain significance	11	117999069	117999069	Human	2	name
26890871	CV838017	single nucleotide variant	NM_001558.4(IL10RA):c.1250A>G (p.Gln417Arg)	Inflammatory bowel disease 28 [RCV001059854]	uncertain significance	11	117999154	117999154	Human	1	name
26916747	CV838018	single nucleotide variant	NM_001558.4(IL10RA):c.1399T>C (p.Ser467Pro)	Inflammatory bowel disease 28 [RCV001040895]	uncertain significance	11	117999303	117999303	Human	1	name
28906700	CV867072	single nucleotide variant	NM_001558.4(IL10RA):c.1414G>A (p.Gly472Ser)	Inflammatory bowel disease 28 [RCV001106803]	uncertain significance	11	117999318	117999318	Human	1	name
38488774	CV947332	single nucleotide variant	NM_001558.4(IL10RA):c.1040C>T (p.Thr347Met)	Inflammatory bowel disease 28 [RCV001238142]	uncertain significance	11	117998944	117998944	Human	1	name
38458138	CV956396	single nucleotide variant	NM_001558.4(IL10RA):c.1103C>T (p.Thr368Ile)	Inflammatory bowel disease 28 [RCV001246242]	uncertain significance	11	117999007	117999007	Human	1	name
126753892	CV994338	single nucleotide variant	NM_001558.4(IL10RA):c.1336T>A (p.Tyr446Asn)	Inflammatory bowel disease 28 [RCV001298001]	uncertain significance	11	117999240	117999240	Human	1	name
126766682	CV994339	single nucleotide variant	NM_001558.4(IL10RA):c.1718G>A (p.Ser573Asn)	Inflammatory bowel disease 28 [RCV001301988]	uncertain significance	11	117999622	117999622	Human	1	name
155940842	CV2038120	duplication	NM_001558.4(IL10RA):c.258_279dup (p.Asn94fs)	Inflammatory bowel disease 28 [RCV002775181]	pathogenic	11	117989510	117989511	Human	1	name
151711656	CV1406647	deletion	NM_000628.5(IL10RB):c.800_801del (p.Lys267fs)	Inflammatory bowel disease 25 [RCV002003863]	uncertain significance	21	33288256	33288257	Human	1	name
156211649	CV2087244	deletion	NM_001558.4(IL10RA):c.439_452del (p.Arg147fs)	Inflammatory bowel disease 28 [RCV002852849]	pathogenic	11	117993311	117993324	Human	1	name
15196891	CV773296	inversion	NM_000628.5(IL10RB):c.138_139inv (p.Lys47Glu)	Inflammatory bowel disease 25 [RCV000934348]	likely benign	21	33268482	33268483	Human		name
152117608	CV1538911	inversion	NM_001558.4(IL10RA):c.1050_1051inv (p.Arg351Gly)	Inflammatory bowel disease 28 [RCV002175143]	likely benign	11	117998954	117998955	Human		name
151805559	CV1393083	deletion	NM_000628.5(IL10RB):c.962_967del (p.Gln321_Gly322del)	Inflammatory bowel disease 25 [RCV001931366]	uncertain significance	21	33296337	33296342	Human	1	name
14726138	CV639727	duplication	NM_001558.4(IL10RA):c.559_579dup (p.His187_Leu193dup)	Inflammatory bowel disease 28 [RCV000815505]	uncertain significance	11	117994018	117994019	Human	1	name
13817636	CV570308	deletion	NM_001558.4(IL10RA):c.1087_1095del (p.Gly363_Ser365del)	Inflammatory bowel disease 28 [RCV000693154]	uncertain significance	11	117998991	117998999	Human	1	name
151730297	CV1396821	deletion	NM_001558.4(IL10RA):c.1181_1237del (p.Asn394_Ala413delinsThr)	Inflammatory bowel disease 28 [RCV001910796]	uncertain significance	11	117999085	117999141	Human	1	name

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