Il22 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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119 records found for search term Il22

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329378355	CV2446978	single nucleotide variant	NM_020525.5(IL22):c.25A>C (p.Ser9Arg)	not provided [RCV004696357]\|not specified [RCV004257819]	uncertain significance	12	68253424	68253424	Human		name
401893448	CV2763417	single nucleotide variant	NM_020525.5(IL22):c.95C>A (p.Ala32Glu)	not specified [RCV004349306]	uncertain significance	12	68253354	68253354	Human		name
156389398	CV2226256	single nucleotide variant	NM_020525.5(IL22):c.262C>T (p.Arg88Cys)	not specified [RCV004099503]	uncertain significance	12	68252638	68252638	Human		name
405804805	CV3271115	single nucleotide variant	NM_020525.5(IL22):c.147G>T (p.Gln49His)	not specified [RCV004405176]	uncertain significance	12	68253302	68253302	Human		name
405804806	CV3271116	single nucleotide variant	NM_020525.5(IL22):c.248T>C (p.Val83Ala)	not specified [RCV004405177]	uncertain significance	12	68252768	68252768	Human		name
405804808	CV3271117	single nucleotide variant	NM_020525.5(IL22):c.255G>A (p.Met85Ile)	not specified [RCV004405178]	uncertain significance	12	68252645	68252645	Human		name
597774584	CV3686480	single nucleotide variant	NM_020525.5(IL22):c.172A>C (p.Met58Leu)	not specified [RCV004929161]	uncertain significance	12	68253277	68253277	Human		name
597774588	CV3686481	single nucleotide variant	NM_020525.5(IL22):c.138C>A (p.Asn46Lys)	not specified [RCV004929162]	uncertain significance	12	68253311	68253311	Human		name
598207487	CV3972223	single nucleotide variant	NM_020525.5(IL22):c.242A>G (p.His81Arg)	not specified [RCV005337982]	likely benign	12	68252774	68252774	Human		name
156251150	CV2196440	single nucleotide variant	NM_020525.5(IL22):c.487G>A (p.Ala163Thr)	not specified [RCV004073741]	uncertain significance	12	68248852	68248852	Human		name
156232566	CV2227692	single nucleotide variant	NM_020525.5(IL22):c.374T>A (p.Leu125His)	not specified [RCV004094082]	uncertain significance	12	68252526	68252526	Human		name
156023847	CV2273809	single nucleotide variant	NM_020525.5(IL22):c.358C>T (p.Pro120Ser)	not specified [RCV004132442]	likely benign	12	68252542	68252542	Human		name
156093728	CV2300244	single nucleotide variant	NM_020525.5(IL22):c.355G>A (p.Val119Met)	not specified [RCV004153210]	uncertain significance	12	68252545	68252545	Human		name
156259958	CV2366418	single nucleotide variant	NM_020525.5(IL22):c.460A>G (p.Lys154Glu)	not specified [RCV004212462]	uncertain significance	12	68251515	68251515	Human		name
401891980	CV2775860	single nucleotide variant	NM_020525.5(IL22):c.530C>T (p.Ala177Val)	not specified [RCV004344893]	uncertain significance	12	68248809	68248809	Human		name
597774580	CV3686479	single nucleotide variant	NM_020525.5(IL22):c.458A>G (p.Lys153Arg)	not specified [RCV004929160]	uncertain significance	12	68251517	68251517	Human		name
15156651	CV725252	single nucleotide variant	NM_020525.5(IL22):c.472A>G (p.Ser158Gly)	not provided [RCV000880672]	benign	12	68248867	68248867	Human		name
404988400	CV2849576	single nucleotide variant	NM_021258.4(IL22RA1):c.*81C>T	not specified [RCV003490433]	benign	1	24120724	24120724	Human		name
404984440	CV2849409	single nucleotide variant	NM_021258.4(IL22RA1):c.44-105G>A	not specified [RCV003489281]	benign	1	24138819	24138819	Human		name
404988328	CV2849487	single nucleotide variant	NM_021258.4(IL22RA1):c.355+58G>A	not specified [RCV003490344]	benign	1	24137073	24137073	Human		name
404989390	CV2849540	single nucleotide variant	NM_021258.4(IL22RA1):c.177-55G>A	not specified [RCV003490397]	benign	1	24137364	24137364	Human		name
404984426	CV2849405	single nucleotide variant	NM_021258.4(IL22RA1):c.135G>A (p.Pro45=)	not specified [RCV003489277]	benign	1	24138623	24138623	Human		name
156154713	CV2328683	single nucleotide variant	NM_052962.3(IL22RA2):c.77A>G (p.His26Arg)	not specified [RCV004177923]	uncertain significance	6	137158467	137158467	Human		name
156071719	CV2365333	single nucleotide variant	NM_021258.4(IL22RA1):c.49G>C (p.Ala17Pro)	not specified [RCV004209418]	uncertain significance	1	24138709	24138709	Human		name
404984452	CV2849411	single nucleotide variant	NM_021258.4(IL22RA1):c.435A>C (p.Pro145=)	not specified [RCV003489283]	benign	1	24134307	24134307	Human		name
404988202	CV2849470	single nucleotide variant	NM_021258.4(IL22RA1):c.936C>T (p.Pro312=)	not specified [RCV003490327]	benign	1	24121594	24121594	Human		name
405804827	CV3271127	single nucleotide variant	NM_021258.4(IL22RA1):c.35C>T (p.Ser12Phe)	not specified [RCV004405188]	uncertain significance	1	24143048	24143048	Human		name
597774614	CV3686487	single nucleotide variant	NM_021258.4(IL22RA1):c.61C>G (p.Pro21Ala)	not specified [RCV004929168]	uncertain significance	1	24138697	24138697	Human		name
597774626	CV3686490	single nucleotide variant	NM_052962.3(IL22RA2):c.97A>T (p.Arg33Trp)	not specified [RCV004929171]	uncertain significance	6	137158447	137158447	Human		name
8624937	CV80055	single nucleotide variant	NM_021258.3(IL22RA1):c.831C>T (p.Phe277=)	Malignant melanoma [RCV000060131]	not provided	1	24121699	24121699	Human		name
150534798	CV1311623	single nucleotide variant	NM_052962.3(IL22RA2):c.115C>T (p.Arg39Ter)	Multisystem inflammatory syndrome in children [RCV001779433]	risk factor	6	137158429	137158429	Human	1	name
156323277	CV2201575	single nucleotide variant	NM_021258.4(IL22RA1):c.218G>A (p.Arg73Gln)	not specified [RCV004080064]	uncertain significance	1	24137268	24137268	Human		name
156337164	CV2228647	single nucleotide variant	NM_052962.3(IL22RA2):c.107T>A (p.Phe36Tyr)	not specified [RCV004092871]	uncertain significance	6	137158437	137158437	Human		name
156288309	CV2229752	single nucleotide variant	NM_021258.4(IL22RA1):c.266C>T (p.Thr89Met)	not specified [RCV004103547]	uncertain significance	1	24137220	24137220	Human		name
156365707	CV2272161	single nucleotide variant	NM_021258.4(IL22RA1):c.181G>A (p.Gly61Arg)	not specified [RCV004124932]	uncertain significance	1	24137305	24137305	Human		name
156083949	CV2343132	single nucleotide variant	NM_021258.4(IL22RA1):c.233C>T (p.Ser78Phe)	not specified [RCV004194768]	uncertain significance	1	24137253	24137253	Human		name
156276075	CV2351898	single nucleotide variant	NM_052962.3(IL22RA2):c.116G>A (p.Arg39Gln)	not specified [RCV004198040]	uncertain significance	6	137158428	137158428	Human		name
156093185	CV2389668	single nucleotide variant	NM_021258.4(IL22RA1):c.130G>A (p.Gly44Arg)	not specified [RCV004243722]	uncertain significance	1	24138628	24138628	Human		name
401762040	CV2699498	single nucleotide variant	NM_021258.4(IL22RA1):c.207G>C (p.Lys69Asn)	not specified [RCV004299710]	uncertain significance	1	24137279	24137279	Human		name
405804823	CV3271125	single nucleotide variant	NM_021258.4(IL22RA1):c.223A>G (p.Thr75Ala)	not specified [RCV004405186]	uncertain significance	1	24137263	24137263	Human		name
405804825	CV3271126	single nucleotide variant	NM_021258.4(IL22RA1):c.242T>A (p.Leu81Gln)	not specified [RCV004405187]	uncertain significance	1	24137244	24137244	Human		name
405804838	CV3271133	single nucleotide variant	NM_052962.3(IL22RA2):c.158T>A (p.Leu53His)	not specified [RCV004405194]	uncertain significance	6	137158386	137158386	Human		name
597774618	CV3686488	single nucleotide variant	NM_021258.4(IL22RA1):c.217C>T (p.Arg73Trp)	not specified [RCV004929169]	uncertain significance	1	24137269	24137269	Human		name
598179940	CV3972232	single nucleotide variant	NM_052962.3(IL22RA2):c.128A>G (p.Asn43Ser)	not specified [RCV005352257]	uncertain significance	6	137158416	137158416	Human		name
15171454	CV718837	single nucleotide variant	NM_021258.4(IL22RA1):c.1188G>A (p.Pro396=)	not provided [RCV000883657]	benign	1	24121342	24121342	Human		name
156305735	CV2252650	single nucleotide variant	NM_021258.4(IL22RA1):c.806T>A (p.Val269Asp)	not specified [RCV004118515]	uncertain significance	1	24121724	24121724	Human		name
155954281	CV2303346	single nucleotide variant	NM_021258.4(IL22RA1):c.833T>G (p.Ile278Ser)	not specified [RCV004159084]	uncertain significance	1	24121697	24121697	Human		name
156298787	CV2310657	single nucleotide variant	NM_052962.3(IL22RA2):c.410C>T (p.Ala137Val)	not specified [RCV004157317]	uncertain significance	6	137155003	137155003	Human		name
156162365	CV2311812	single nucleotide variant	NM_021258.4(IL22RA1):c.431C>T (p.Thr144Met)	not specified [RCV004170661]	uncertain significance	1	24134311	24134311	Human		name
156179736	CV2324292	single nucleotide variant	NM_021258.4(IL22RA1):c.919T>C (p.Ser307Pro)	not specified [RCV004177020]	uncertain significance	1	24121611	24121611	Human		name
156036014	CV2335042	single nucleotide variant	NM_021258.4(IL22RA1):c.953G>A (p.Arg318Gln)	not specified [RCV004184581]	uncertain significance	1	24121577	24121577	Human		name
156277811	CV2352106	single nucleotide variant	NM_021258.4(IL22RA1):c.844G>A (p.Val282Ile)	not specified [RCV004191198]	uncertain significance	1	24121686	24121686	Human		name
156343288	CV2364090	single nucleotide variant	NM_052962.3(IL22RA2):c.452G>A (p.Arg151Gln)	not specified [RCV004221471]	uncertain significance	6	137154961	137154961	Human		name
156187755	CV2378101	single nucleotide variant	NM_021258.4(IL22RA1):c.803G>A (p.Arg268Gln)	not specified [RCV004232657]	uncertain significance	1	24121727	24121727	Human		name
156149170	CV2394556	single nucleotide variant	NM_052962.3(IL22RA2):c.449C>T (p.Pro150Leu)	not specified [RCV004240909]	uncertain significance	6	137154964	137154964	Human		name
156153949	CV2395034	single nucleotide variant	NM_021258.4(IL22RA1):c.458G>A (p.Arg153Gln)	not specified [RCV004236722]	likely benign	1	24134284	24134284	Human		name
329360228	CV2446618	single nucleotide variant	NM_021258.4(IL22RA1):c.909G>T (p.Gln303His)	not specified [RCV004251508]	uncertain significance	1	24121621	24121621	Human		name
329368992	CV2450490	single nucleotide variant	NM_052962.3(IL22RA2):c.470A>C (p.Glu157Ala)	not specified [RCV004265410]	uncertain significance	6	137154943	137154943	Human		name
401778859	CV2705787	single nucleotide variant	NM_052962.3(IL22RA2):c.737C>T (p.Pro246Leu)	not specified [RCV004318620]	uncertain significance	6	137145679	137145679	Human		name
401760487	CV2705939	single nucleotide variant	NM_052962.3(IL22RA2):c.674C>T (p.Ala225Val)	not specified [RCV004320864]	likely benign	6	137145742	137145742	Human		name
401763016	CV2710409	single nucleotide variant	NM_021258.4(IL22RA1):c.757T>C (p.Tyr253His)	not specified [RCV004317567]	uncertain significance	1	24123337	24123337	Human		name
401771479	CV2711709	single nucleotide variant	NM_021258.4(IL22RA1):c.697G>A (p.Gly233Arg)	not specified [RCV004309376]	uncertain significance	1	24123397	24123397	Human		name
401762269	CV2723379	single nucleotide variant	NM_052962.3(IL22RA2):c.697C>T (p.Pro233Ser)	not specified [RCV004329586]	uncertain significance	6	137145719	137145719	Human		name
401725163	CV2725725	single nucleotide variant	NM_021258.4(IL22RA1):c.442G>A (p.Ala148Thr)	not specified [RCV004322417]	uncertain significance	1	24134300	24134300	Human		name
401877514	CV2761162	single nucleotide variant	NM_021258.4(IL22RA1):c.776C>T (p.Ala259Val)	not specified [RCV004341047]	uncertain significance	1	24123318	24123318	Human		name
401899122	CV2786031	single nucleotide variant	NM_052962.3(IL22RA2):c.676G>T (p.Val226Phe)	not specified [RCV004359856]	uncertain significance	6	137145740	137145740	Human		name
404987917	CV2849509	single nucleotide variant	NM_021258.4(IL22RA1):c.613G>A (p.Val205Ile)	not specified [RCV003490366]	benign	1	24128198	24128198	Human		name
405804829	CV3271128	single nucleotide variant	NM_021258.4(IL22RA1):c.376G>A (p.Val126Met)	not specified [RCV004405189]	uncertain significance	1	24134366	24134366	Human		name
405804831	CV3271129	single nucleotide variant	NM_021258.4(IL22RA1):c.385A>G (p.Ile129Val)	not specified [RCV004405190]	uncertain significance	1	24134357	24134357	Human		name
405804832	CV3271130	single nucleotide variant	NM_021258.4(IL22RA1):c.419A>G (p.His140Arg)	not specified [RCV004405191]	uncertain significance	1	24134323	24134323	Human		name
405804834	CV3271131	single nucleotide variant	NM_021258.4(IL22RA1):c.674G>A (p.Arg225Gln)	not specified [RCV004405192]	uncertain significance	1	24123420	24123420	Human		name
405804836	CV3271132	single nucleotide variant	NM_021258.4(IL22RA1):c.821C>A (p.Pro274Gln)	not specified [RCV004405193]	uncertain significance	1	24121709	24121709	Human		name
405804839	CV3271134	single nucleotide variant	NM_052962.3(IL22RA2):c.397G>A (p.Gly133Arg)	not specified [RCV004405195]	uncertain significance	6	137155016	137155016	Human	1	name
405804841	CV3271135	single nucleotide variant	NM_052962.3(IL22RA2):c.683T>C (p.Ile228Thr)	not specified [RCV004405196]	uncertain significance	6	137145733	137145733	Human		name
405804843	CV3271136	single nucleotide variant	NM_052962.3(IL22RA2):c.734A>G (p.Gln245Arg)	not specified [RCV004405197]	uncertain significance	6	137145682	137145682	Human		name
405804845	CV3271137	single nucleotide variant	NM_052962.3(IL22RA2):c.775T>C (p.Cys259Arg)	not specified [RCV004405198]	uncertain significance	6	137145641	137145641	Human		name
407515864	CV3444575	single nucleotide variant	NM_021258.4(IL22RA1):c.640C>G (p.Pro214Ala)	not specified [RCV004628021]	uncertain significance	1	24128171	24128171	Human		name
407515878	CV3444579	single nucleotide variant	NM_021258.4(IL22RA1):c.730G>A (p.Ala244Thr)	not specified [RCV004628025]	uncertain significance	1	24123364	24123364	Human		name
407515882	CV3444580	single nucleotide variant	NM_021258.4(IL22RA1):c.677C>T (p.Thr226Ile)	not specified [RCV004628026]	uncertain significance	1	24123417	24123417	Human		name
407515889	CV3444582	single nucleotide variant	NM_052962.3(IL22RA2):c.729A>G (p.Ile243Met)	not specified [RCV004628028]	uncertain significance	6	137145687	137145687	Human		name
407515895	CV3444583	single nucleotide variant	NM_052962.3(IL22RA2):c.389C>T (p.Pro130Leu)	not specified [RCV004628029]	uncertain significance	6	137155024	137155024	Human		name
597774592	CV3686482	single nucleotide variant	NM_021258.4(IL22RA1):c.448G>A (p.Asp150Asn)	not specified [RCV004929163]	uncertain significance	1	24134294	24134294	Human		name
597774596	CV3686483	single nucleotide variant	NM_021258.4(IL22RA1):c.953G>C (p.Arg318Pro)	not specified [RCV004929164]	uncertain significance	1	24121577	24121577	Human		name
597774602	CV3686484	single nucleotide variant	NM_021258.4(IL22RA1):c.947C>T (p.Pro316Leu)	not specified [RCV004929165]	uncertain significance	1	24121583	24121583	Human		name
597774610	CV3686486	single nucleotide variant	NM_021258.4(IL22RA1):c.835C>G (p.Gln279Glu)	not specified [RCV004929167]	uncertain significance	1	24121695	24121695	Human		name
598179901	CV3972224	single nucleotide variant	NM_021258.4(IL22RA1):c.841C>G (p.His281Asp)	not specified [RCV005352250]	uncertain significance	1	24121689	24121689	Human		name
598179906	CV3972225	single nucleotide variant	NM_021258.4(IL22RA1):c.653G>A (p.Arg218Gln)	not specified [RCV005352251]	uncertain significance	1	24128158	24128158	Human		name
598179917	CV3972228	single nucleotide variant	NM_021258.4(IL22RA1):c.572T>C (p.Leu191Pro)	not specified [RCV005352253]	uncertain significance	1	24128239	24128239	Human		name
598179923	CV3972229	single nucleotide variant	NM_021258.4(IL22RA1):c.956A>G (p.His319Arg)	not specified [RCV005352254]	uncertain significance	1	24121574	24121574	Human		name
598179928	CV3972230	single nucleotide variant	NM_021258.4(IL22RA1):c.484G>C (p.Asp162His)	not specified [RCV005352255]	uncertain significance	1	24134258	24134258	Human		name
598179935	CV3972231	single nucleotide variant	NM_021258.4(IL22RA1):c.517C>T (p.Arg173Cys)	not specified [RCV005352256]	uncertain significance	1	24134225	24134225	Human		name
598207498	CV3972233	single nucleotide variant	NM_052962.3(IL22RA2):c.577G>A (p.Val193Ile)	not specified [RCV005337984]	likely benign	6	137147787	137147787	Human		name
15171362	CV718839	single nucleotide variant	NM_021258.4(IL22RA1):c.388T>C (p.Ser130Pro)	not provided [RCV000883640]	benign	1	24134354	24134354	Human		name
156198971	CV2255952	single nucleotide variant	NM_021258.4(IL22RA1):c.1720T>C (p.Ser574Pro)	not specified [RCV004122403]	uncertain significance	1	24120810	24120810	Human		name
156212925	CV2260000	single nucleotide variant	NM_021258.4(IL22RA1):c.1352C>A (p.Thr451Asn)	not specified [RCV004119016]	uncertain significance	1	24121178	24121178	Human		name
155993662	CV2286323	single nucleotide variant	NM_021258.4(IL22RA1):c.1018G>A (p.Val340Met)	not specified [RCV004146271]	likely benign	1	24121512	24121512	Human		name
156068336	CV2317980	single nucleotide variant	NM_021258.4(IL22RA1):c.1032G>T (p.Gln344His)	not specified [RCV004177099]	uncertain significance	1	24121498	24121498	Human		name
156165777	CV2319890	single nucleotide variant	NM_021258.4(IL22RA1):c.1499C>T (p.Ser500Phe)	not specified [RCV004167771]	uncertain significance	1	24121031	24121031	Human		name
156057873	CV2322887	single nucleotide variant	NM_021258.4(IL22RA1):c.1295A>G (p.Gln432Arg)	not specified [RCV004185341]	uncertain significance	1	24121235	24121235	Human		name
156085761	CV2340481	single nucleotide variant	NM_021258.4(IL22RA1):c.1463C>T (p.Thr488Ile)	not specified [RCV004197205]	uncertain significance	1	24121067	24121067	Human		name
329376328	CV2425074	single nucleotide variant	NM_021258.4(IL22RA1):c.1213G>A (p.Val405Ile)	not specified [RCV004248970]	uncertain significance	1	24121317	24121317	Human		name
401741766	CV2710253	single nucleotide variant	NM_021258.4(IL22RA1):c.1568C>T (p.Ser523Leu)	not specified [RCV004317148]	uncertain significance	1	24120962	24120962	Human		name
401889645	CV2758353	single nucleotide variant	NM_021258.4(IL22RA1):c.1526T>A (p.Met509Lys)	not specified [RCV004341703]	uncertain significance	1	24121004	24121004	Human		name
404984125	CV2849414	single nucleotide variant	NM_021258.4(IL22RA1):c.1552C>G (p.Arg518Gly)	not specified [RCV003489286]	benign	1	24120978	24120978	Human		name
405804812	CV3271119	single nucleotide variant	NM_021258.4(IL22RA1):c.1081C>T (p.Pro361Ser)	not specified [RCV004405180]	uncertain significance	1	24121449	24121449	Human		name
405804814	CV3271120	single nucleotide variant	NM_021258.4(IL22RA1):c.1153G>T (p.Val385Phe)	not specified [RCV004405181]	uncertain significance	1	24121377	24121377	Human		name
405804816	CV3271121	single nucleotide variant	NM_021258.4(IL22RA1):c.1274T>A (p.Leu425His)	not specified [RCV004405182]	uncertain significance	1	24121256	24121256	Human		name
405804817	CV3271122	single nucleotide variant	NM_021258.4(IL22RA1):c.1289A>C (p.Gln430Pro)	not specified [RCV004405183]	uncertain significance	1	24121241	24121241	Human		name
405804819	CV3271123	single nucleotide variant	NM_021258.4(IL22RA1):c.1495C>T (p.Leu499Phe)	not specified [RCV004405184]	uncertain significance	1	24121035	24121035	Human		name
407515854	CV3444572	single nucleotide variant	NM_021258.4(IL22RA1):c.1222G>A (p.Glu408Lys)	not specified [RCV004628018]	uncertain significance	1	24121308	24121308	Human		name
407515861	CV3444574	single nucleotide variant	NM_021258.4(IL22RA1):c.1151A>C (p.Lys384Thr)	not specified [RCV004628020]	uncertain significance	1	24121379	24121379	Human		name
407515867	CV3444576	single nucleotide variant	NM_021258.4(IL22RA1):c.1078G>C (p.Gly360Arg)	not specified [RCV004628022]	likely benign	1	24121452	24121452	Human		name
407515870	CV3444577	single nucleotide variant	NM_021258.4(IL22RA1):c.1460G>A (p.Gly487Glu)	not specified [RCV004628023]	uncertain significance	1	24121070	24121070	Human		name
407515874	CV3444578	single nucleotide variant	NM_021258.4(IL22RA1):c.1517G>A (p.Gly506Asp)	not specified [RCV004628024]	uncertain significance	1	24121013	24121013	Human		name
407515885	CV3444581	single nucleotide variant	NM_021258.4(IL22RA1):c.1106C>G (p.Thr369Ser)	not specified [RCV004628027]	uncertain significance	1	24121424	24121424	Human		name
597774606	CV3686485	single nucleotide variant	NM_021258.4(IL22RA1):c.1322T>A (p.Met441Lys)	not specified [RCV004929166]	uncertain significance	1	24121208	24121208	Human		name
597774622	CV3686489	single nucleotide variant	NM_021258.4(IL22RA1):c.1379A>C (p.Glu460Ala)	not specified [RCV004929170]	uncertain significance	1	24121151	24121151	Human		name
598179912	CV3972227	single nucleotide variant	NM_021258.4(IL22RA1):c.1665G>T (p.Gln555His)	not specified [RCV005352252]	uncertain significance	1	24120865	24120865	Human		name
15194588	CV696620	single nucleotide variant	NM_021258.4(IL22RA1):c.1219A>G (p.Met407Val)	not provided [RCV000955687]	benign	1	24121311	24121311	Human		name

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