Il3 Variant Search Result - Rat Genome Database

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523 records found for search term Il3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15190451	CV730329	single nucleotide variant	NM_000588.4(IL3):c.294+9A>T	not provided [RCV000888102]	benign	5	132062410	132062410	Human		name
15127099	CV709609	single nucleotide variant	NM_000588.4(IL3):c.7C>T (p.Arg3Cys)	not provided [RCV000963845]	benign	5	132060713	132060713	Human		name
401872871	CV2764390	single nucleotide variant	NM_000588.4(IL3):c.16G>A (p.Val6Ile)	not specified [RCV004338961]	likely benign	5	132060722	132060722	Human		name
15190448	CV721205	single nucleotide variant	NM_000588.4(IL3):c.189C>T (p.Asp63=)	not provided [RCV000888101]	benign	5	132060993	132060993	Human		name
407516004	CV3444608	single nucleotide variant	NM_000588.4(IL3):c.77C>T (p.Thr26Met)	not specified [RCV004628054]	uncertain significance	5	132060783	132060783	Human		name
597774845	CV3686521	single nucleotide variant	NM_000588.4(IL3):c.43C>A (p.Arg15Ser)	not specified [RCV004929202]	likely benign	5	132060749	132060749	Human		name
598180082	CV3972268	single nucleotide variant	NM_000588.4(IL3):c.50G>A (p.Gly17Glu)	not specified [RCV005352282]	uncertain significance	5	132060756	132060756	Human		name
156078019	CV2291703	single nucleotide variant	NM_000588.4(IL3):c.182G>A (p.Gly61Glu)	not specified [RCV004157989]	likely benign	5	132060986	132060986	Human		name
156249128	CV2358826	single nucleotide variant	NM_000588.4(IL3):c.159G>T (p.Leu53Phe)	not specified [RCV004212174]	uncertain significance	5	132060865	132060865	Human		name
598207571	CV3972269	single nucleotide variant	NM_000588.4(IL3):c.119A>G (p.Asp40Gly)	not specified [RCV005337995]	uncertain significance	5	132060825	132060825	Human		name
15108037	CV721204	single nucleotide variant	NM_000588.4(IL3):c.179A>G (p.Asn60Ser)	not provided [RCV000893594]	likely benign	5	132060983	132060983	Human		name
156175873	CV2205281	single nucleotide variant	NM_000588.4(IL3):c.380G>T (p.Arg127Leu)	not specified [RCV004079901]	uncertain significance	5	132062712	132062712	Human		name
156236070	CV2245482	single nucleotide variant	NM_000588.4(IL3):c.352A>G (p.Ile118Val)	not specified [RCV004109260]	uncertain significance	5	132062684	132062684	Human		name
156163346	CV2246640	single nucleotide variant	NM_000588.4(IL3):c.369G>C (p.Trp123Cys)	not provided [RCV004695434]\|not specified [RCV004110378]	uncertain significance	5	132062701	132062701	Human		name
156049514	CV2271804	single nucleotide variant	NM_000588.4(IL3):c.335C>T (p.Thr112Met)	not specified [RCV004130638]	uncertain significance	5	132062566	132062566	Human		name
405804926	CV3271180	single nucleotide variant	NM_000588.4(IL3):c.379C>T (p.Arg127Trp)	not specified [RCV004405241]	uncertain significance	5	132062711	132062711	Human		name
405804927	CV3271181	single nucleotide variant	NM_000588.4(IL3):c.386A>G (p.Lys129Arg)	not specified [RCV004405242]	uncertain significance	5	132062718	132062718	Human		name
405804929	CV3271182	single nucleotide variant	NM_000588.4(IL3):c.449C>T (p.Ala150Val)	not specified [RCV004405243]	uncertain significance	5	132062781	132062781	Human		name
597774843	CV3686520	single nucleotide variant	NM_000588.4(IL3):c.448G>A (p.Ala150Thr)	not specified [RCV004929201]	uncertain significance	5	132062780	132062780	Human		name
598180093	CV3972271	single nucleotide variant	NM_000588.4(IL3):c.434C>T (p.Thr145Met)	not specified [RCV005352284]	likely benign	5	132062766	132062766	Human		name
11591590	CV283791	single nucleotide variant	NM_012275.3(IL36RN):c.*6C>T	Generalized pustular psoriasis [RCV000330599]	uncertain significance	2	113062683	113062683	Human	1	name
153305904	CV1686720	duplication	NM_012275.3(IL36RN):c.*15dup	Autoinflammatory syndrome [RCV002264631]	uncertain significance	2	113062686	113062687	Human	1	name
11660124	CV283788	single nucleotide variant	NM_012275.3(IL36RN):c.-47G>A	Generalized pustular psoriasis [RCV000364420]	uncertain significance	2	113059222	113059222	Human	1	name
126745263	CV1003173	single nucleotide variant	NM_012275.3(IL36RN):c.29+6T>C	Generalized pustular psoriasis [RCV001325154]	uncertain significance	2	113059473	113059473	Human	1	name
127243765	CV1054904	single nucleotide variant	NM_012275.3(IL36RN):c.29+1G>A	Generalized pustular psoriasis [RCV001377160]	likely pathogenic	2	113059468	113059468	Human	1	name
153304014	CV1686722	single nucleotide variant	NM_012275.3(IL36RN):c.29+3G>A	Autoinflammatory syndrome [RCV002262009]	uncertain significance	2	113059470	113059470	Human	1	name
156100393	CV2051081	single nucleotide variant	NM_012275.3(IL36RN):c.30-2A>G	Generalized pustular psoriasis [RCV002824537]	likely pathogenic	2	113060850	113060850	Human	1	name
155950919	CV2084482	single nucleotide variant	NM_012275.3(IL36RN):c.29+7G>A	Generalized pustular psoriasis [RCV002880496]	likely benign	2	113059474	113059474	Human	1	name
11588113	CV281597	single nucleotide variant	NM_012275.3(IL36RN):c.*946T>C	Generalized pustular psoriasis [RCV000300576]\|not provided [RCV004708360]	benign	2	113063623	113063623	Human	1	name
11586327	CV282258	single nucleotide variant	NM_012275.3(IL36RN):c.*308T>G	Generalized pustular psoriasis [RCV000287352]\|not provided [RCV004710834]	likely benign\|uncertain significance	2	113062985	113062985	Human	1	name
11585837	CV282259	single nucleotide variant	NM_012275.3(IL36RN):c.*401A>T	Acrodermatitis continua suppurativa of Hallopeau [RCV003326133]\|Generalized pustular psoriasis [RCV000283822]\|not provided [RCV004709861]	benign\|uncertain significance	2	113063078	113063078	Human	1	name
11596575	CV282260	single nucleotide variant	NM_012275.3(IL36RN):c.*478T>C	Generalized pustular psoriasis [RCV000384030]\|not provided [RCV004708356]	benign	2	113063155	113063155	Human	1	name
11598068	CV282269	single nucleotide variant	NM_012275.3(IL36RN):c.*935G>C	Generalized pustular psoriasis [RCV000401244]	benign\|likely benign	2	113063612	113063612	Human	1	name
11582827	CV283604	single nucleotide variant	NM_012275.3(IL36RN):c.*222T>C	Acrodermatitis continua suppurativa of Hallopeau [RCV003326130]\|Generalized pustular psoriasis [RCV000262540]\|not provided [RCV004708352]	benign\|uncertain significance	2	113062899	113062899	Human	1	name
11595622	CV283611	single nucleotide variant	NM_012275.3(IL36RN):c.*281G>A	Generalized pustular psoriasis [RCV000372461]	likely benign\|uncertain significance	2	113062958	113062958	Human	1	name
11590923	CV283612	single nucleotide variant	NM_012275.3(IL36RN):c.*326C>A	Acrodermatitis continua suppurativa of Hallopeau [RCV003326132]\|Generalized pustular psoriasis [RCV000323693]\|not provided [RCV004708354]	benign\|uncertain significance	2	113063003	113063003	Human	1	name
11581624	CV283620	single nucleotide variant	NM_012275.3(IL36RN):c.*401A>C	Generalized pustular psoriasis [RCV000377776]\|not provided [RCV004694463]	uncertain significance	2	113063078	113063078	Human	1	name
11586646	CV283621	single nucleotide variant	NM_012275.3(IL36RN):c.*560C>G	Acrodermatitis continua suppurativa of Hallopeau [RCV003326135]\|Generalized pustular psoriasis [RCV000289570]\|not provided [RCV004708357]	benign\|uncertain significance	2	113063237	113063237	Human	1	name
11593523	CV283623	single nucleotide variant	NM_012275.3(IL36RN):c.*863C>T	Generalized pustular psoriasis [RCV000349605]\|not provided [RCV004708359]	benign	2	113063540	113063540	Human	1	name
11581138	CV283792	single nucleotide variant	NM_012275.3(IL36RN):c.*185C>T	Generalized pustular psoriasis [RCV000357253]	uncertain significance	2	113062862	113062862	Human	1	name
11590289	CV283793	single nucleotide variant	NM_012275.3(IL36RN):c.*276A>G	Acrodermatitis continua suppurativa of Hallopeau [RCV003326131]\|Generalized pustular psoriasis [RCV000317835]\|not provided [RCV004708353]	benign\|uncertain significance	2	113062953	113062953	Human	1	name
11593383	CV283794	single nucleotide variant	NM_012275.3(IL36RN):c.*418A>G	Acrodermatitis continua suppurativa of Hallopeau [RCV003326134]\|Generalized pustular psoriasis [RCV000348147]\|not provided [RCV004708355]	benign\|uncertain significance	2	113063095	113063095	Human	1	name
11593026	CV283795	single nucleotide variant	NM_012275.3(IL36RN):c.*581C>G	Generalized pustular psoriasis [RCV000344589]	uncertain significance	2	113063258	113063258	Human	1	name
11597645	CV283800	single nucleotide variant	NM_012275.3(IL36RN):c.*828G>A	Generalized pustular psoriasis [RCV000396604]\|not provided [RCV004708358]	benign\|likely benign	2	113063505	113063505	Human	1	name
11653985	CV283804	single nucleotide variant	NM_012275.3(IL36RN):c.*857A>G	Generalized pustular psoriasis [RCV000314216]	uncertain significance	2	113063534	113063534	Human	1	name
405025949	CV2871755	single nucleotide variant	NM_012275.3(IL36RN):c.30-1G>T	Generalized pustular psoriasis [RCV003528986]	likely pathogenic	2	113060851	113060851	Human	1	name
14696160	CV612426	single nucleotide variant	NM_014438.5(IL36B):c.391+2T>C	High myopia [RCV000785707]	uncertain significance	2	113026101	113026101	Human	2	name
15125594	CV778873	single nucleotide variant	NM_014439.4(IL37):c.265+10A>C	not provided [RCV000963604]	likely benign	2	112917258	112917258	Human		name
28872033	CV880863	single nucleotide variant	NM_012275.3(IL36RN):c.*106G>A	Generalized pustular psoriasis [RCV001132077]	uncertain significance	2	113062783	113062783	Human	1	name
28873733	CV880864	single nucleotide variant	NM_012275.3(IL36RN):c.*298G>A	Generalized pustular psoriasis [RCV001133014]	uncertain significance	2	113062975	113062975	Human	1	name
28881872	CV880865	single nucleotide variant	NM_012275.3(IL36RN):c.*426G>T	Generalized pustular psoriasis [RCV001136451]	uncertain significance	2	113063103	113063103	Human	1	name
28867768	CV880866	single nucleotide variant	NM_012275.3(IL36RN):c.*594T>C	Generalized pustular psoriasis [RCV001129465]	uncertain significance	2	113063271	113063271	Human	1	name
28867771	CV880867	single nucleotide variant	NM_012275.3(IL36RN):c.*720G>T	Generalized pustular psoriasis [RCV001129466]	uncertain significance	2	113063397	113063397	Human	1	name
28867774	CV880868	single nucleotide variant	NM_012275.3(IL36RN):c.*866G>A	Generalized pustular psoriasis [RCV001129467]	uncertain significance	2	113063543	113063543	Human	1	name
28867777	CV880869	single nucleotide variant	NM_012275.3(IL36RN):c.*883T>C	Generalized pustular psoriasis [RCV001129468]	uncertain significance	2	113063560	113063560	Human	1	name
28881590	CV882783	single nucleotide variant	NM_012275.3(IL36RN):c.29+5G>A	Generalized pustular psoriasis [RCV001136347]	uncertain significance	2	113059472	113059472	Human	1	name
127283620	CV1067800	single nucleotide variant	NM_012275.3(IL36RN):c.116-5C>G	Generalized pustular psoriasis [RCV001411927]	likely benign	2	113062119	113062119	Human	1	name
127291245	CV1111069	single nucleotide variant	NM_012275.3(IL36RN):c.115+7G>A	Generalized pustular psoriasis [RCV001458661]	likely benign	2	113060944	113060944	Human	1	name
150445080	CV1278093	single nucleotide variant	NM_033439.4(IL33):c.91+1165C>T	not provided [RCV001707236]	benign	9	6242950	6242950	Human		name
151791549	CV1341298	single nucleotide variant	NM_012275.3(IL36RN):c.115+4G>A	Generalized pustular psoriasis [RCV001866294]	uncertain significance	2	113060941	113060941	Human	1	name
151776105	CV1450523	single nucleotide variant	NM_012275.3(IL36RN):c.29+15C>G	Generalized pustular psoriasis [RCV001915448]	likely benign	2	113059482	113059482	Human	1	name
152032456	CV1629417	single nucleotide variant	NM_012275.3(IL36RN):c.29+15C>A	Generalized pustular psoriasis [RCV002106369]	likely benign	2	113059482	113059482	Human	1	name
152115335	CV1653963	single nucleotide variant	NM_012275.3(IL36RN):c.30-12C>T	Generalized pustular psoriasis [RCV002097399]	likely benign	2	113060840	113060840	Human	1	name
156274443	CV2046309	single nucleotide variant	NM_012275.3(IL36RN):c.30-13C>T	Generalized pustular psoriasis [RCV002770163]	likely benign	2	113060839	113060839	Human	1	name
11594601	CV281598	single nucleotide variant	NM_012275.3(IL36RN):c.*1399T>C	Generalized pustular psoriasis [RCV000361128]\|not provided [RCV004709862]	benign	2	113064076	113064076	Human	1	name
11591292	CV281600	single nucleotide variant	NM_012275.3(IL36RN):c.*1660G>A	Generalized pustular psoriasis [RCV000327629]	likely benign\|uncertain significance	2	113064337	113064337	Human	1	name
11586461	CV281606	single nucleotide variant	NM_012275.3(IL36RN):c.*1844A>G	Generalized pustular psoriasis [RCV000287914]	uncertain significance	2	113064521	113064521	Human	1	name
11596931	CV281607	single nucleotide variant	NM_012275.3(IL36RN):c.*1881G>T	Generalized pustular psoriasis [RCV000388188]\|not provided [RCV004708363]	benign\|likely benign	2	113064558	113064558	Human	1	name
11663392	CV281611	single nucleotide variant	NM_012275.3(IL36RN):c.*1942C>G	Generalized pustular psoriasis [RCV000395732]	uncertain significance	2	113064619	113064619	Human	1	name
11659155	CV282270	single nucleotide variant	NM_012275.3(IL36RN):c.*1051T>C	Generalized pustular psoriasis [RCV000355488]	uncertain significance	2	113063728	113063728	Human	1	name
11582556	CV282272	single nucleotide variant	NM_012275.3(IL36RN):c.*1082C>A	Generalized pustular psoriasis [RCV000260623]\|not provided [RCV004708361]	benign\|likely benign	2	113063759	113063759	Human	1	name
11587709	CV282274	single nucleotide variant	NM_012275.3(IL36RN):c.*1258C>A	Generalized pustular psoriasis [RCV000297076]	uncertain significance	2	113063935	113063935	Human	1	name
11587868	CV282289	single nucleotide variant	NM_012275.3(IL36RN):c.*1987G>A	Generalized pustular psoriasis [RCV000298498]\|not provided [RCV004708365]	benign\|likely benign	2	113064664	113064664	Human	1	name
11663827	CV283590	single nucleotide variant	NM_012275.3(IL36RN):c.30-14T>A	Generalized pustular psoriasis [RCV000399615]	uncertain significance	2	113060838	113060838	Human	1	name
11645601	CV283631	single nucleotide variant	NM_012275.3(IL36RN):c.*1540G>A	Generalized pustular psoriasis [RCV000266487]	uncertain significance	2	113064217	113064217	Human	1	name
11654916	CV283638	single nucleotide variant	NM_012275.3(IL36RN):c.*1585A>G	Generalized pustular psoriasis [RCV000321778]	uncertain significance	2	113064262	113064262	Human	1	name
11587160	CV283639	single nucleotide variant	NM_012275.3(IL36RN):c.*1902T>C	Generalized pustular psoriasis [RCV000292716]\|not provided [RCV004710835]	likely benign\|uncertain significance	2	113064579	113064579	Human	1	name
11595945	CV283807	single nucleotide variant	NM_012275.3(IL36RN):c.*1633C>T	Generalized pustular psoriasis [RCV000376457]\|not provided [RCV004708362]	benign\|likely benign	2	113064310	113064310	Human	1	name
11584259	CV283819	single nucleotide variant	NM_012275.3(IL36RN):c.*1634A>G	Generalized pustular psoriasis [RCV000272602]\|not provided [RCV004709863]	benign\|likely benign	2	113064311	113064311	Human	1	name
11596425	CV283822	single nucleotide variant	NM_012275.3(IL36RN):c.*1763G>A	Generalized pustular psoriasis [RCV000382330]	likely benign\|uncertain significance	2	113064440	113064440	Human	1	name
11593806	CV283825	single nucleotide variant	NM_012275.3(IL36RN):c.*1849T>A	Generalized pustular psoriasis [RCV000352261]	uncertain significance	2	113064526	113064526	Human	1	name
11592422	CV283826	single nucleotide variant	NM_012275.3(IL36RN):c.*1914C>T	Generalized pustular psoriasis [RCV000338307]\|not provided [RCV004708364]	benign\|likely benign	2	113064591	113064591	Human	1	name
11592005	CV283851	single nucleotide variant	NM_012275.3(IL36RN):c.*1995T>C	Generalized pustular psoriasis [RCV000334663]	uncertain significance	2	113064672	113064672	Human	1	name
405022963	CV2858666	single nucleotide variant	NM_012275.3(IL36RN):c.116-6C>T	Generalized pustular psoriasis [RCV003528582]	likely benign	2	113062118	113062118	Human	1	name
405194477	CV2958549	single nucleotide variant	NM_012275.3(IL36RN):c.30-18C>A	Generalized pustular psoriasis [RCV003641276]	likely benign	2	113060834	113060834	Human	1	name
405217208	CV3124754	single nucleotide variant	NM_012275.3(IL36RN):c.115+9T>C	Generalized pustular psoriasis [RCV003824117]	likely benign	2	113060946	113060946	Human	1	name
8570705	CV48518	single nucleotide variant	NM_012275.3(IL36RN):c.115+6T>C	Acrodermatitis continua suppurativa of Hallopeau [RCV002508136]\|Autoinflammatory syndrome [RCV002262597]\|Generalized pustular psoriasis [RCV000033132]\|IL36RN-related disorder [RCV003914894]\|not provided [RCV005411304]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity	2	113060943	113060943	Human	3	name , trait , alternate_id
8570705	CV48518	single nucleotide variant	NM_012275.3(IL36RN):c.115+6T>C	Acrodermatitis continua suppurativa of Hallopeau [RCV002508136]\|Autoinflammatory syndrome [RCV002262597]\|Generalized pustular psoriasis [RCV000033132]\|IL36RN-related disorder [RCV003914894]\|not provided [RCV005411304]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity	2	113060943	113060944	Human	3	name , trait , alternate_id
14397134	CV612557	single nucleotide variant	NM_012275.3(IL36RN):c.115+5G>A	Autoinflammatory syndrome [RCV002263965]\|Generalized pustular psoriasis [RCV001054362]\|not provided [RCV000762280]	uncertain significance	2	113060942	113060942	Human	2	name
14693633	CV620734	single nucleotide variant	NM_012275.3(IL36RN):c.-28+1G>A	Acrodermatitis continua suppurativa of Hallopeau [RCV002477782]	uncertain significance	2	113059242	113059242	Human	1	name
15157802	CV743807	single nucleotide variant	NM_012275.3(IL36RN):c.244-6C>T	Autoinflammatory syndrome [RCV002264070]\|Generalized pustular psoriasis [RCV000902603]	likely benign\|uncertain significance	2	113062447	113062447	Human	2	name
15153338	CV744955	single nucleotide variant	NM_001376923.1(IL32):c.16-4G>A	not provided [RCV000901741]	benign	16	3067373	3067373	Human		name
15149055	CV744958	duplication	NM_001376923.1(IL32):c.54+8dup	not provided [RCV000900852]	likely benign	16	3067422	3067423	Human		name
15201711	CV760309	single nucleotide variant	NM_001376923.1(IL32):c.16-5C>T	not provided [RCV000913219]	likely benign	16	3067372	3067372	Human		name
15145150	CV779123	single nucleotide variant	NM_139017.7(IL31RA):c.773-9T>C	IL31RA-related disorder [RCV003916224]\|not provided [RCV000966946]	benign	5	55896341	55896341	Human	1	name , trait , alternate_id
26914395	CV850832	single nucleotide variant	NM_012275.3(IL36RN):c.244-5G>A	Autoinflammatory syndrome [RCV002264148]\|Generalized pustular psoriasis [RCV001037461]	uncertain significance	2	113062448	113062448	Human	2	name
28872229	CV880870	single nucleotide variant	NM_012275.3(IL36RN):c.*1244A>G	Generalized pustular psoriasis [RCV001132190]	uncertain significance	2	113063921	113063921	Human	1	name
28873920	CV880871	single nucleotide variant	NM_012275.3(IL36RN):c.*1405G>T	Generalized pustular psoriasis [RCV001133119]	uncertain significance	2	113064082	113064082	Human	1	name
28873922	CV880872	single nucleotide variant	NM_012275.3(IL36RN):c.*1641C>G	Generalized pustular psoriasis [RCV001133120]	uncertain significance	2	113064318	113064318	Human	1	name
28873926	CV880873	single nucleotide variant	NM_012275.3(IL36RN):c.*1698G>A	Generalized pustular psoriasis [RCV001133121]	uncertain significance	2	113064375	113064375	Human	1	name
28876917	CV880874	single nucleotide variant	NM_012275.3(IL36RN):c.*1866T>C	Generalized pustular psoriasis [RCV001134592]	uncertain significance	2	113064543	113064543	Human	1	name
28876924	CV880875	single nucleotide variant	NM_012275.3(IL36RN):c.*1891G>A	Generalized pustular psoriasis [RCV001134593]	uncertain significance	2	113064568	113064568	Human	1	name
150521263	CV1290219	single nucleotide variant	NM_139017.7(IL31RA):c.606+29A>T	Amyloidosis, primary localized cutaneous, 2 [RCV001731032]\|not provided [RCV004717842]	benign	5	55883224	55883224	Human	1	name
152160722	CV1522912	single nucleotide variant	NM_012275.3(IL36RN):c.244-15C>T	Generalized pustular psoriasis [RCV002140870]	likely benign	2	113062438	113062438	Human	1	name
152166511	CV1566410	single nucleotide variant	NM_012275.3(IL36RN):c.244-13C>T	Generalized pustular psoriasis [RCV002160663]	likely benign	2	113062440	113062440	Human	1	name
152163250	CV1600789	single nucleotide variant	NM_012275.3(IL36RN):c.243+16T>C	Generalized pustular psoriasis [RCV002141290]	likely benign	2	113062267	113062267	Human	1	name
152124559	CV1646021	single nucleotide variant	NM_012275.3(IL36RN):c.115+15A>G	Generalized pustular psoriasis [RCV002217222]	likely benign	2	113060952	113060952	Human	1	name
152107709	CV1657359	single nucleotide variant	NM_012275.3(IL36RN):c.244-13C>A	Generalized pustular psoriasis [RCV002215042]	likely benign	2	113062440	113062440	Human	1	name
156324643	CV1972600	single nucleotide variant	NM_012275.3(IL36RN):c.244-17C>T	Generalized pustular psoriasis [RCV002600451]	likely benign	2	113062436	113062436	Human	1	name
156369901	CV2007648	single nucleotide variant	NM_012275.3(IL36RN):c.244-10C>A	Generalized pustular psoriasis [RCV002676822]	likely benign	2	113062443	113062443	Human	1	name
401931159	CV2795665	single nucleotide variant	NM_012275.3(IL36RN):c.-27-49C>G	not specified [RCV003391227]	benign	2	113059363	113059363	Human		name
401931166	CV2795666	single nucleotide variant	NM_012275.3(IL36RN):c.-27-47A>C	not specified [RCV003391228]	benign	2	113059365	113059365	Human		name
401906772	CV2795690	single nucleotide variant	NM_012275.3(IL36RN):c.29+137C>T	not specified [RCV003397042]	benign	2	113059604	113059604	Human		name
404987482	CV2849438	single nucleotide variant	NM_012275.3(IL36RN):c.116-87T>C	not specified [RCV003490295]	benign	2	113062037	113062037	Human		name
405026325	CV2872447	single nucleotide variant	NM_012275.3(IL36RN):c.115+14C>T	Generalized pustular psoriasis [RCV003529019]	likely benign	2	113060951	113060951	Human	1	name
405202465	CV3071994	single nucleotide variant	NM_012275.3(IL36RN):c.116-11C>T	Generalized pustular psoriasis [RCV003642351]	likely benign	2	113062113	113062113	Human	1	name
405293143	CV3221295	single nucleotide variant	NM_139017.7(IL31RA):c.606+10G>T	IL31RA-related disorder [RCV003966817]	likely benign	5	55883205	55883205	Human		name , trait , alternate_id
598226124	CV3895740	single nucleotide variant	NM_139017.7(IL31RA):c.1070-3C>G	Amyloidosis, primary localized cutaneous, 2 [RCV005362046]	uncertain significance	5	55906103	55906103	Human	1	name
15171336	CV778282	single nucleotide variant	NM_001393494.1(IL34):c.241-5C>T	not provided [RCV000949814]	benign	16	70656955	70656955	Human		name
8627799	CV82943	single nucleotide variant	NM_001012631.1(IL32):c.55-46G>A	Malignant melanoma [RCV000063023]	not provided	16	3067508	3067508	Human		name
150521264	CV1290220	single nucleotide variant	NM_139017.7(IL31RA):c.1819-26T>G	Amyloidosis, primary localized cutaneous, 2 [RCV001731033]\|not provided [RCV004717843]	benign	5	55916618	55916618	Human	1	name
401906776	CV2795691	single nucleotide variant	NM_012275.3(IL36RN):c.115+118G>A	not specified [RCV003397043]	benign	2	113061055	113061055	Human		name
11589347	CV282255	single nucleotide variant	NM_173170.1(IL36RN):c.-27-299G>C	Generalized pustular psoriasis [RCV000310031]	uncertain significance	2	113059113	113059113	Human	1	name
401917688	CV2827763	single nucleotide variant	NM_139017.7(IL31RA):c.63+1922C>T	not provided [RCV003429639]	likely benign	5	55853555	55853555	Human		name
405267930	CV3202648	single nucleotide variant	NM_139017.7(IL31RA):c.1501+79C>T	IL31RA-related disorder [RCV003911868]	benign	5	55908490	55908490	Human		name , trait , alternate_id
11665638	CV353536	single nucleotide variant	NM_173170.1(IL36RN):c.-27-318G>A	Generalized pustular psoriasis [RCV000283910]	uncertain significance	2	113059094	113059094	Human	1	name
15192877	CV776339	single nucleotide variant	NM_001376923.1(IL32):c.142-10C>T	not provided [RCV000933206]	likely benign	16	3068170	3068170	Human		name
8635770	CV90993	single nucleotide variant	NM_001012631.1(IL32):c.114+11T>A	Malignant melanoma [RCV000071091]	not provided	16	3067624	3067624	Human		name
8696102	CV97382	single nucleotide variant	NM_001012631.1(IL32):c.114+13C>T	Malignant melanoma [RCV000128476]	not provided	16	3067626	3067626	Human		name
8648976	CV110626	single nucleotide variant	NM_001278568.1(IL36G):c.-20+184C>T	Lung cancer [RCV000091149]	uncertain significance	2	112978262	112978262	Human		name
152107010	CV1664604	deletion	NM_012275.3(IL36RN):c.244-9_244-6del	Generalized pustular psoriasis [RCV002173845]	likely benign	2	113062443	113062446	Human	1	name
8631671	CV86875	single nucleotide variant	NM_001242638.1(IL31RA):c.1444+147G>A	Malignant melanoma [RCV000066966]	not provided	5	55908558	55908558	Human		name
405280400	CV3200765	single nucleotide variant	NM_001393494.1(IL34):c.468G>A (p.Leu156=)	IL34-related disorder [RCV003977390]	likely benign	16	70659683	70659683	Human		name , trait , alternate_id
405276140	CV3206602	single nucleotide variant	NM_001393494.1(IL34):c.169T>C (p.Tyr57His)	IL34-related disorder [RCV003917047]	likely benign	16	70656608	70656608	Human	2	name , trait , alternate_id
405276140	CV3206602	single nucleotide variant	NM_001393494.1(IL34):c.169T>C (p.Tyr57His)	IL34-related disorder [RCV003917047]	likely benign	16	70656608	70656609	Human	2	name , trait , alternate_id
405276815	CV3206809	single nucleotide variant	NM_001393494.1(IL34):c.695C>T (p.Pro232Leu)	IL34-related disorder [RCV003917238]	likely benign	16	70660153	70660153	Human		name , trait , alternate_id
126745257	CV1003176	single nucleotide variant	NM_012275.3(IL36RN):c.351G>A (p.Pro117=)	Generalized pustular psoriasis [RCV001324834]\|IL36RN-related disorder [RCV003898310]	likely benign\|uncertain significance	2	113062560	113062560	Human	1	name , trait , alternate_id
127231835	CV1087603	single nucleotide variant	NM_139017.7(IL31RA):c.1449T>G (p.Gly483=)	Amyloidosis, primary localized cutaneous, 2 [RCV001421007]\|IL31RA-related disorder [RCV003973266]\|not provided [RCV004716718]	benign	5	55908359	55908359	Human	1	name , trait , alternate_id
127237858	CV1089526	single nucleotide variant	NM_012275.3(IL36RN):c.240A>G (p.Leu80=)	Generalized pustular psoriasis [RCV001433640]\|IL36RN-related disorder [RCV003930922]	likely benign	2	113062248	113062248	Human	1	name , trait , alternate_id
11578162	CV283603	single nucleotide variant	NM_012275.3(IL36RN):c.363G>A (p.Leu121=)	Autoinflammatory syndrome [RCV002263598]\|Generalized pustular psoriasis [RCV000275463]\|IL36RN-related disorder [RCV003912386]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	2	113062572	113062572	Human	2	name , trait , alternate_id
405272243	CV3199240	single nucleotide variant	NM_139017.7(IL31RA):c.1764C>T (p.Thr588=)	IL31RA-related disorder [RCV003914191]	benign	5	55914874	55914874	Human		name , trait , alternate_id
405260614	CV3204164	single nucleotide variant	NM_139017.7(IL31RA):c.804G>A (p.Leu268=)	IL31RA-related disorder [RCV003944028]	likely benign	5	55896381	55896381	Human		name , trait , alternate_id
405256043	CV3208548	single nucleotide variant	NM_139017.7(IL31RA):c.33G>C (p.Thr11=)	IL31RA-related disorder [RCV003939626]	likely benign	5	55851603	55851603	Human		name , trait , alternate_id
405283417	CV3217057	single nucleotide variant	NM_139017.7(IL31RA):c.2014G>C (p.Val672Leu)	IL31RA-related disorder [RCV003979188]	benign	5	55916839	55916839	Human		name , trait , alternate_id
405287922	CV3218033	single nucleotide variant	NM_139017.7(IL31RA):c.1586G>A (p.Ser529Asn)	IL31RA-related disorder [RCV003982157]	benign	5	55910616	55910616	Human		name , trait , alternate_id
405278843	CV3220484	single nucleotide variant	NM_139017.7(IL31RA):c.307A>G (p.Asn103Asp)	IL31RA-related disorder [RCV003976676]	benign	5	55872304	55872304	Human		name , trait , alternate_id
8602239	CV39447	single nucleotide variant	NM_012275.3(IL36RN):c.338C>T (p.Ser113Leu)	Acrodermatitis continua suppurativa of Hallopeau [RCV002288518]\|Autoinflammatory syndrome [RCV002262572]\|Generalized pustular psoriasis [RCV000023447]\|IL36RN-related disorder [RCV003415734]\|not provided [RCV000513043]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	2	113062547	113062547	Human	2	name , trait , alternate_id
8602240	CV39448	single nucleotide variant	NM_012275.3(IL36RN):c.142C>T (p.Arg48Trp)	Acrodermatitis continua suppurativa of Hallopeau [RCV002508134]\|Generalized pustular psoriasis [RCV000023448]\|IL36RN-related disorder [RCV004755749]\|not provided [RCV001701724]	pathogenic\|uncertain significance	2	113062150	113062150	Human	1	name , trait , alternate_id
15195350	CV749532	single nucleotide variant	NM_139017.7(IL31RA):c.709G>A (p.Val237Ile)	IL31RA-related disorder [RCV003950738]\|not provided [RCV000911392]\|not specified [RCV004028988]	benign\|likely benign\|uncertain significance	5	55890072	55890072	Human	1	name , trait , alternate_id
405707512	CV3225390	single nucleotide variant	NM_014439.4(IL37):c.3G>A (p.Met1Ile)	Inflammatory bowel disease (infantile ulcerative colitis) 31, autosomal recessive [RCV003990444]	uncertain significance	2	112913015	112913015	Human	1	name
13619075	CV516398	single nucleotide variant	NM_012275.3(IL36RN):c.6C>T (p.Val2=)	Autoinflammatory syndrome [RCV002263871]\|Generalized pustular psoriasis [RCV000635398]\|not provided [RCV004597839]	benign\|likely benign\|conflicting interpretations of pathogenicity	2	113059444	113059444	Human	2	name
8629796	CV84943	single nucleotide variant	NM_014438.4(IL36B):c.15G>A (p.Arg5=)	Malignant melanoma [RCV000065025]	not provided	2	113031154	113031154	Human		name
127324940	CV1131930	single nucleotide variant	NM_012275.3(IL36RN):c.18G>A (p.Ala6=)	Generalized pustular psoriasis [RCV001485628]	likely benign	2	113059456	113059456	Human	1	name
155967047	CV2391302	single nucleotide variant	NM_033439.4(IL33):c.10A>G (p.Lys4Glu)	not specified [RCV004237667]	uncertain significance	9	6241704	6241704	Human		name
597774919	CV3686542	single nucleotide variant	NM_033439.4(IL33):c.11A>C (p.Lys4Thr)	not specified [RCV004929223]	uncertain significance	9	6241705	6241705	Human		name
15163058	CV711995	single nucleotide variant	NM_033439.4(IL33):c.150C>A (p.Gly50=)	not provided [RCV000970400]	benign	9	6250532	6250532	Human		name
15151570	CV737161	single nucleotide variant	NM_033439.4(IL33):c.273G>C (p.Val91=)	not provided [RCV000901390]	benign	9	6251195	6251195	Human		name
127326361	CV1111067	single nucleotide variant	NM_012275.3(IL36RN):c.75G>A (p.Gln25=)	Generalized pustular psoriasis [RCV001468723]	likely benign	2	113060897	113060897	Human	1	name
151835144	CV1474675	single nucleotide variant	NM_012275.3(IL36RN):c.8T>C (p.Leu3Pro)	Generalized pustular psoriasis [RCV001920891]	uncertain significance	2	113059446	113059446	Human	1	name
156391249	CV2385196	single nucleotide variant	NM_033439.4(IL33):c.43G>A (p.Ala15Thr)	not specified [RCV004228445]	uncertain significance	9	6241737	6241737	Human		name
401924830	CV2812254	single nucleotide variant	NM_014439.4(IL37):c.312G>A (p.Glu104=)	not provided [RCV003436120]	likely benign	2	112917681	112917681	Human		name
405190821	CV3043313	single nucleotide variant	NM_012275.3(IL36RN):c.42G>A (p.Ser14=)	Generalized pustular psoriasis [RCV003640817]	likely benign	2	113060864	113060864	Human	1	name
405804975	CV3271207	single nucleotide variant	NM_033439.4(IL33):c.47A>G (p.Lys16Arg)	not specified [RCV004405268]	uncertain significance	9	6241741	6241741	Human		name
407516052	CV3444623	single nucleotide variant	NM_014439.4(IL37):c.35T>C (p.Met12Thr)	not specified [RCV004628068]	uncertain significance	2	112913047	112913047	Human		name
596927509	CV3540002	single nucleotide variant	NM_012275.3(IL36RN):c.4G>T (p.Val2Phe)	not provided [RCV004790994]	uncertain significance	2	113059442	113059442	Human		name
597939007	CV3775221	deletion	NM_012275.3(IL36RN):c.16del (p.Ala6fs)	Generalized pustular psoriasis [RCV005118047]	pathogenic	2	113059451	113059451	Human	1	name
598207619	CV3972294	single nucleotide variant	NM_033439.4(IL33):c.84G>C (p.Lys28Asn)	not specified [RCV005338002]	uncertain significance	9	6241778	6241778	Human		name
15178334	CV709947	single nucleotide variant	NM_139017.7(IL31RA):c.54G>A (p.Pro18=)	not provided [RCV000973642]	benign\|likely benign	5	55851624	55851624	Human		name
8625104	CV80223	single nucleotide variant	NM_014439.3(IL37):c.52G>A (p.Glu18Lys)	Malignant melanoma [RCV000060299]	not provided	2	112913064	112913064	Human		name
8625105	CV80224	single nucleotide variant	NM_014440.1(IL36A):c.180G>A (p.Gly60=)	Malignant melanoma [RCV000060300]	not provided	2	113006653	113006653	Human		name
8629795	CV84942	single nucleotide variant	NM_014438.4(IL36B):c.16G>A (p.Glu6Lys)	Malignant melanoma [RCV000065024]	not provided	2	113031153	113031153	Human		name
127312060	CV1111068	single nucleotide variant	NM_012275.3(IL36RN):c.102G>A (p.Gly34=)	Generalized pustular psoriasis [RCV001457060]	likely benign	2	113060924	113060924	Human	1	name
150521315	CV1290218	single nucleotide variant	NM_139017.7(IL31RA):c.129C>T (p.Pro43=)	Amyloidosis, primary localized cutaneous, 2 [RCV001731031]\|not provided [RCV004716798]	benign	5	55859574	55859574	Human	1	name
151872202	CV1430019	single nucleotide variant	NM_012275.3(IL36RN):c.142C>A (p.Arg48=)	Generalized pustular psoriasis [RCV002019101]	uncertain significance	2	113062150	113062150	Human	1	name
152086730	CV1571456	single nucleotide variant	NM_012275.3(IL36RN):c.228G>A (p.Pro76=)	Generalized pustular psoriasis [RCV002131520]	likely benign	2	113062236	113062236	Human	1	name
152159176	CV1595332	single nucleotide variant	NM_012275.3(IL36RN):c.168C>T (p.Pro56=)	Generalized pustular psoriasis [RCV002103466]	likely benign	2	113062176	113062176	Human	1	name
152036039	CV1648400	single nucleotide variant	NM_012275.3(IL36RN):c.165C>A (p.Ser55=)	Generalized pustular psoriasis [RCV002125338]	likely benign	2	113062173	113062173	Human	1	name
156131053	CV1885512	single nucleotide variant	NM_012275.3(IL36RN):c.17C>T (p.Ala6Val)	Generalized pustular psoriasis [RCV003081839]	uncertain significance	2	113059455	113059455	Human	1	name
155955604	CV1936318	single nucleotide variant	NM_014439.4(IL37):c.133T>A (p.Phe45Ile)	not provided [RCV002511982]	uncertain significance	2	112913842	112913842	Human		name
156055398	CV2023835	single nucleotide variant	NM_012275.3(IL36RN):c.165C>T (p.Ser55=)	Generalized pustular psoriasis [RCV002736647]	likely benign	2	113062173	113062173	Human	1	name
156242837	CV2086061	single nucleotide variant	NM_012275.3(IL36RN):c.282A>G (p.Glu94=)	Generalized pustular psoriasis [RCV002876659]	likely benign	2	113062491	113062491	Human	1	name
155934091	CV2229081	single nucleotide variant	NM_173178.3(IL36B):c.61G>A (p.Val21Met)	not specified [RCV004098852]	uncertain significance	2	113031108	113031108	Human		name
155999719	CV2257667	single nucleotide variant	NM_014439.4(IL37):c.227A>G (p.Asn76Ser)	not specified [RCV004127758]	uncertain significance	2	112917210	112917210	Human		name
156263829	CV2282608	single nucleotide variant	NM_014440.3(IL36A):c.49G>T (p.Asp17Tyr)	not specified [RCV004135170]	uncertain significance	2	113006012	113006012	Human		name
156194819	CV2309469	single nucleotide variant	NM_014439.4(IL37):c.182G>T (p.Ser61Ile)	not specified [RCV004158875]	uncertain significance	2	112917165	112917165	Human		name
156210301	CV2314233	single nucleotide variant	NM_033439.4(IL33):c.296C>T (p.Ser99Leu)	not specified [RCV004166602]	uncertain significance	9	6251218	6251218	Human		name
155916806	CV2336210	single nucleotide variant	NM_033439.4(IL33):c.164A>G (p.Lys55Arg)	not specified [RCV004191967]	uncertain significance	9	6250546	6250546	Human		name
156142362	CV2358488	single nucleotide variant	NM_014439.4(IL37):c.170C>G (p.Pro57Arg)	not specified [RCV004207376]	uncertain significance	2	112917153	112917153	Human		name
329356476	CV2430769	single nucleotide variant	NM_033439.4(IL33):c.142C>T (p.Arg48Cys)	not specified [RCV004253947]	uncertain significance	9	6250524	6250524	Human		name
401767782	CV2677814	single nucleotide variant	NM_033439.4(IL33):c.244C>T (p.Leu82Phe)	not specified [RCV004294312]	likely benign	9	6251166	6251166	Human		name
401753613	CV2722527	single nucleotide variant	NM_019618.4(IL36G):c.92A>C (p.Asn31Thr)	not specified [RCV004322911]	uncertain significance	2	112979257	112979257	Human		name
405195814	CV2972573	single nucleotide variant	NM_012275.3(IL36RN):c.148C>T (p.Leu50=)	Generalized pustular psoriasis [RCV003641454]	likely benign	2	113062156	113062156	Human	1	name
405095501	CV3119001	single nucleotide variant	NM_012275.3(IL36RN):c.210T>C (p.Cys70=)	Generalized pustular psoriasis [RCV003811452]	likely benign	2	113062218	113062218	Human	1	name
405003736	CV3120762	single nucleotide variant	NM_012275.3(IL36RN):c.144G>C (p.Arg48=)	Generalized pustular psoriasis [RCV003828365]	likely benign	2	113062152	113062152	Human	1	name
405804969	CV3271204	single nucleotide variant	NM_033439.4(IL33):c.266C>T (p.Ser89Phe)	not specified [RCV004405265]	uncertain significance	9	6251188	6251188	Human		name
405804982	CV3271211	single nucleotide variant	NM_001393494.1(IL34):c.7C>T (p.Arg3Trp)	not specified [RCV004405272]	uncertain significance	16	70646954	70646954	Human		name
405804989	CV3271215	single nucleotide variant	NM_014440.3(IL36A):c.64G>T (p.Val22Leu)	not specified [RCV004405276]	uncertain significance	2	113006027	113006027	Human		name
405804996	CV3271219	single nucleotide variant	NM_019618.4(IL36G):c.38G>C (p.Arg13Thr)	not specified [RCV004405280]	uncertain significance	2	112978676	112978676	Human		name
405805002	CV3271222	single nucleotide variant	NM_014439.4(IL37):c.107C>A (p.Pro36Gln)	not specified [RCV004405283]	uncertain significance	2	112913816	112913816	Human		name
405805004	CV3271223	single nucleotide variant	NM_014439.4(IL37):c.170C>T (p.Pro57Leu)	not specified [RCV004405284]	uncertain significance	2	112917153	112917153	Human		name
405805006	CV3271224	single nucleotide variant	NM_014439.4(IL37):c.196G>T (p.Asp66Tyr)	not specified [RCV004405285]	uncertain significance	2	112917179	112917179	Human		name
405805008	CV3271225	single nucleotide variant	NM_014439.4(IL37):c.201C>G (p.His67Gln)	not specified [RCV004405286]	likely benign	2	112917184	112917184	Human		name
405805009	CV3271226	single nucleotide variant	NM_014439.4(IL37):c.217G>A (p.Asp73Asn)	not specified [RCV004405287]	uncertain significance	2	112917200	112917200	Human		name
405805011	CV3271227	single nucleotide variant	NM_014439.4(IL37):c.259C>T (p.Arg87Cys)	not specified [RCV004405288]	uncertain significance	2	112917242	112917242	Human		name
407516045	CV3444621	single nucleotide variant	NM_014439.4(IL37):c.154G>A (p.Val52Met)	not specified [RCV004628066]	uncertain significance	2	112917137	112917137	Human		name
597774962	CV3686554	single nucleotide variant	NM_014440.3(IL36A):c.62G>T (p.Arg21Leu)	not specified [RCV004929235]	uncertain significance	2	113006025	113006025	Human		name
597774977	CV3686560	single nucleotide variant	NM_019618.4(IL36G):c.43G>T (p.Val15Phe)	not specified [RCV004929241]	uncertain significance	2	112978681	112978681	Human		name
597959619	CV3811421	single nucleotide variant	NM_012275.3(IL36RN):c.150G>A (p.Leu50=)	Generalized pustular psoriasis [RCV005163267]	likely benign	2	113062158	113062158	Human	1	name
597929610	CV3862228	single nucleotide variant	NM_012275.3(IL36RN):c.237A>C (p.Thr79=)	Generalized pustular psoriasis [RCV005206469]	likely benign	2	113062245	113062245	Human	1	name
598207670	CV3972310	single nucleotide variant	NM_014439.4(IL37):c.104A>T (p.Glu35Val)	not specified [RCV005338009]	uncertain significance	2	112913813	112913813	Human		name
15156113	CV696980	single nucleotide variant	NM_014439.4(IL37):c.124A>G (p.Thr42Ala)	not provided [RCV000946630]	benign	2	112913833	112913833	Human		name
15188577	CV743508	single nucleotide variant	NM_002183.4(IL3RA):c.408C>T (p.Tyr136=)	not provided [RCV000909406]	benign	X	1352209	1352209	Human		name
15188577	CV743508	single nucleotide variant	NM_002183.4(IL3RA):c.408C>T (p.Tyr136=)	not provided [RCV000909406]	benign	Y	1352209	1352209	Human		name
15111667	CV762160	single nucleotide variant	NM_012275.3(IL36RN):c.291C>T (p.Ser97=)	Generalized pustular psoriasis [RCV000938793]	likely benign	2	113062500	113062500	Human	1	name
126745079	CV1003174	single nucleotide variant	NM_012275.3(IL36RN):c.40T>G (p.Ser14Ala)	Generalized pustular psoriasis [RCV001314071]	uncertain significance	2	113060862	113060862	Human	1	name
126912651	CV1037637	single nucleotide variant	NM_139017.7(IL31RA):c.59A>G (p.Asn20Ser)	not provided [RCV001356700]	uncertain significance	5	55851629	55851629	Human		name
126922299	CV1040509	single nucleotide variant	NM_012275.3(IL36RN):c.29G>A (p.Arg10Gln)	Autoinflammatory syndrome [RCV002264281]\|Generalized pustular psoriasis [RCV001364509]	uncertain significance	2	113059467	113059467	Human	2	name
127283020	CV1089527	single nucleotide variant	NM_012275.3(IL36RN):c.375T>C (p.Pro125=)	Generalized pustular psoriasis [RCV001448216]	likely benign	2	113062584	113062584	Human	1	name
127319144	CV1111070	single nucleotide variant	NM_012275.3(IL36RN):c.348C>T (p.Tyr116=)	Generalized pustular psoriasis [RCV001466461]	likely benign	2	113062557	113062557	Human	1	name
127287848	CV1163226	single nucleotide variant	NM_014439.4(IL37):c.530T>C (p.Ile177Thr)	Inflammatory bowel disease [RCV001527668]	pathogenic	2	112918682	112918682	Human	2	name
152124722	CV1532213	single nucleotide variant	NM_012275.3(IL36RN):c.387G>A (p.Gln129=)	Generalized pustular psoriasis [RCV002118300]	likely benign	2	113062596	113062596	Human	1	name
152137724	CV1570708	single nucleotide variant	NM_012275.3(IL36RN):c.447C>T (p.Phe149=)	Generalized pustular psoriasis [RCV002119938]	likely benign	2	113062656	113062656	Human	1	name
152074404	CV1620388	single nucleotide variant	NM_012275.3(IL36RN):c.381C>T (p.Ala127=)	Autoinflammatory syndrome [RCV002264460]\|Generalized pustular psoriasis [RCV002111898]	likely benign\|uncertain significance	2	113062590	113062590	Human	2	name
9687106	CV171469	single nucleotide variant	NM_033439.4(IL33):c.712G>A (p.Val238Met)	Prostate cancer [RCV000149325]	uncertain significance	9	6256067	6256067	Human	2	name
156154516	CV1957542	single nucleotide variant	NM_012275.3(IL36RN):c.91C>A (p.Leu31Met)	Generalized pustular psoriasis [RCV002573009]	uncertain significance	2	113060913	113060913	Human	1	name
156365623	CV2020869	single nucleotide variant	NM_012275.3(IL36RN):c.307C>A (p.Arg103=)	Generalized pustular psoriasis [RCV002721163]	likely benign	2	113062516	113062516	Human	1	name
156150813	CV2131729	single nucleotide variant	NM_012275.3(IL36RN):c.366C>T (p.Cys122=)	Generalized pustular psoriasis [RCV002982645]	likely benign	2	113062575	113062575	Human	1	name
156298451	CV2191167	single nucleotide variant	NM_012275.3(IL36RN):c.435C>T (p.Pro145=)	Generalized pustular psoriasis [RCV003061845]	likely benign	2	113062644	113062644	Human	1	name
156400564	CV2199266	single nucleotide variant	NM_173178.3(IL36B):c.237G>C (p.Gln79His)	not specified [RCV004082621]	uncertain significance	2	113028963	113028963	Human		name
155947228	CV2234787	single nucleotide variant	NM_014440.3(IL36A):c.101C>T (p.Pro34Leu)	not specified [RCV004111228]	uncertain significance	2	113006064	113006064	Human		name
155968760	CV2262030	single nucleotide variant	NM_033439.4(IL33):c.571G>C (p.Asp191His)	not specified [RCV004126513]	uncertain significance	9	6254512	6254512	Human		name
156054877	CV2308717	single nucleotide variant	NM_019618.4(IL36G):c.217G>A (p.Asp73Asn)	not specified [RCV004169043]	uncertain significance	2	112980065	112980065	Human		name
155980754	CV2336957	single nucleotide variant	NM_014439.4(IL37):c.308C>T (p.Ala103Val)	not provided [RCV003435931]\|not specified [RCV004192731]	likely benign\|uncertain significance	2	112917677	112917677	Human		name
156054516	CV2344640	single nucleotide variant	NM_019618.4(IL36G):c.259T>C (p.Tyr87His)	not specified [RCV004197408]	uncertain significance	2	112980107	112980107	Human		name
156249927	CV2359005	single nucleotide variant	NM_014440.3(IL36A):c.193C>A (p.Leu65Met)	not specified [RCV004212332]	uncertain significance	2	113006666	113006666	Human		name
155954651	CV2389797	single nucleotide variant	NM_019618.4(IL36G):c.178A>G (p.Thr60Ala)	not specified [RCV004236024]	uncertain significance	2	112980026	112980026	Human		name
329399674	CV2444108	single nucleotide variant	NM_014440.3(IL36A):c.161C>A (p.Thr54Asn)	not specified [RCV004260850]	uncertain significance	2	113006634	113006634	Human		name
329396928	CV2463666	single nucleotide variant	NM_033439.4(IL33):c.757G>C (p.Asp253His)	not specified [RCV004277459]	uncertain significance	9	6256112	6256112	Human		name
329353004	CV2468165	single nucleotide variant	NM_019618.4(IL36G):c.140G>A (p.Arg47Gln)	not specified [RCV004275752]	uncertain significance	2	112979305	112979305	Human		name
401746526	CV2694875	single nucleotide variant	NM_014440.3(IL36A):c.130A>G (p.Ile44Val)	not specified [RCV004300945]	likely benign	2	113006603	113006603	Human		name
401761885	CV2713933	single nucleotide variant	NM_033439.4(IL33):c.610G>A (p.Glu204Lys)	not specified [RCV004315358]	uncertain significance	9	6254551	6254551	Human		name
401880033	CV2765153	single nucleotide variant	NM_014440.3(IL36A):c.113G>A (p.Arg38His)	not specified [RCV004339685]	uncertain significance	2	113006076	113006076	Human		name
401868071	CV2787716	single nucleotide variant	NM_173178.3(IL36B):c.254A>G (p.Gln85Arg)	not specified [RCV004356634]	uncertain significance	2	113028946	113028946	Human		name
401917689	CV2827764	single nucleotide variant	NM_139017.7(IL31RA):c.819G>A (p.Ala273=)	not provided [RCV003429640]	likely benign	5	55896396	55896396	Human		name
405015426	CV2916770	single nucleotide variant	NM_012275.3(IL36RN):c.97G>A (p.Ala33Thr)	Generalized pustular psoriasis [RCV003527685]	uncertain significance	2	113060919	113060919	Human	1	name
405089280	CV3167781	single nucleotide variant	NM_012275.3(IL36RN):c.441A>G (p.Thr147=)	Generalized pustular psoriasis [RCV003852171]	likely benign	2	113062650	113062650	Human	1	name
405804935	CV3271185	single nucleotide variant	NM_001014336.2(IL31):c.183C>G (p.Gly61=)	not specified [RCV004405246]	likely benign	12	122172724	122172724	Human		name
405804937	CV3271186	single nucleotide variant	NM_001014336.2(IL31):c.183C>T (p.Gly61=)	not specified [RCV004405247]	likely benign	12	122172724	122172724	Human		name
405804939	CV3271187	single nucleotide variant	NM_001014336.2(IL31):c.26C>T (p.Thr9Met)	not specified [RCV004405248]	uncertain significance	12	122173983	122173983	Human		name
405804971	CV3271205	single nucleotide variant	NM_033439.4(IL33):c.471T>G (p.Asp157Glu)	not specified [RCV004405266]	uncertain significance	9	6253553	6253553	Human		name
405804973	CV3271206	single nucleotide variant	NM_033439.4(IL33):c.478T>A (p.Leu160Ile)	not specified [RCV004405267]	uncertain significance	9	6253560	6253560	Human		name
405804977	CV3271208	single nucleotide variant	NM_033439.4(IL33):c.536G>C (p.Gly179Ala)	not specified [RCV004405269]	uncertain significance	9	6254477	6254477	Human		name
405804983	CV3271212	single nucleotide variant	NM_014440.3(IL36A):c.214C>G (p.Leu72Val)	not specified [RCV004405273]	uncertain significance	2	113006687	113006687	Human		name
405804985	CV3271213	single nucleotide variant	NM_014440.3(IL36A):c.251C>T (p.Thr84Ile)	not specified [RCV004405274]	uncertain significance	2	113006724	113006724	Human		name
405804991	CV3271216	single nucleotide variant	NM_173178.3(IL36B):c.208G>A (p.Asp70Asn)	not specified [RCV004405277]	likely benign	2	113028992	113028992	Human		name
405804993	CV3271217	single nucleotide variant	NM_019618.4(IL36G):c.184A>G (p.Lys62Glu)	not specified [RCV004405278]	uncertain significance	2	112980032	112980032	Human		name
405805015	CV3271229	single nucleotide variant	NM_014439.4(IL37):c.302C>A (p.Ala101Asp)	not specified [RCV004405290]	uncertain significance	2	112917671	112917671	Human		name
407516028	CV3444616	single nucleotide variant	NM_033439.4(IL33):c.719T>C (p.Ile240Thr)	not specified [RCV004628061]	uncertain significance	9	6256074	6256074	Human		name
407516031	CV3444617	single nucleotide variant	NM_033439.4(IL33):c.299G>A (p.Gly100Glu)	not specified [RCV004628062]	uncertain significance	9	6251221	6251221	Human		name
407516042	CV3444620	single nucleotide variant	NM_014440.3(IL36A):c.212A>G (p.Asn71Ser)	not specified [RCV004628065]	uncertain significance	2	113006685	113006685	Human		name
407516049	CV3444622	single nucleotide variant	NM_014439.4(IL37):c.326T>C (p.Ile109Thr)	not specified [RCV004628067]	uncertain significance	2	112917695	112917695	Human		name
597774899	CV3686537	single nucleotide variant	NM_033439.4(IL33):c.471T>A (p.Asp157Glu)	not specified [RCV004929218]	uncertain significance	9	6253553	6253553	Human		name
597774903	CV3686538	single nucleotide variant	NM_033439.4(IL33):c.457G>C (p.Asp153His)	not specified [RCV004929219]	uncertain significance	9	6252979	6252979	Human		name
597774907	CV3686539	single nucleotide variant	NM_033439.4(IL33):c.331T>A (p.Ser111Thr)	not specified [RCV004929220]	uncertain significance	9	6251253	6251253	Human		name
597774911	CV3686540	single nucleotide variant	NM_033439.4(IL33):c.689T>C (p.Phe230Ser)	not specified [RCV004929221]	uncertain significance	9	6256044	6256044	Human		name
597774915	CV3686541	single nucleotide variant	NM_033439.4(IL33):c.409G>A (p.Ala137Thr)	not specified [RCV004929222]	uncertain significance	9	6252931	6252931	Human		name
597774967	CV3686557	single nucleotide variant	NM_019618.4(IL36G):c.280C>G (p.Gln94Glu)	not specified [RCV004929238]	uncertain significance	2	112980128	112980128	Human		name
597774971	CV3686558	single nucleotide variant	NM_019618.4(IL36G):c.182G>T (p.Cys61Phe)	not specified [RCV004929239]	uncertain significance	2	112980030	112980030	Human		name
597940793	CV3769009	single nucleotide variant	NM_012275.3(IL36RN):c.372G>A (p.Val124=)	Generalized pustular psoriasis [RCV005118504]	likely benign	2	113062581	113062581	Human	1	name
597922479	CV3843258	single nucleotide variant	NM_012275.3(IL36RN):c.318G>A (p.Gly106=)	Generalized pustular psoriasis [RCV005184550]	likely benign	2	113062527	113062527	Human	1	name
597866089	CV3857747	deletion	NM_012275.3(IL36RN):c.273del (p.Ala92fs)	Generalized pustular psoriasis [RCV005196694]	pathogenic	2	113062482	113062482	Human	1	name
8602238	CV39446	single nucleotide variant	NM_012275.3(IL36RN):c.80T>C (p.Leu27Pro)	Acrodermatitis continua suppurativa of Hallopeau [RCV002508133]\|Generalized pustular psoriasis [RCV000023446]\|not provided [RCV001090265]	pathogenic	2	113060902	113060902	Human	1	name
598180122	CV3972279	single nucleotide variant	NM_139017.7(IL31RA):c.71C>A (p.Pro24His)	not specified [RCV005352289]	uncertain significance	5	55859516	55859516	Human		name
598207627	CV3972295	single nucleotide variant	NM_033439.4(IL33):c.437A>G (p.Tyr146Cys)	not specified [RCV005338003]	uncertain significance	9	6252959	6252959	Human		name
598180203	CV3972296	single nucleotide variant	NM_033439.4(IL33):c.560G>A (p.Ser187Asn)	not specified [RCV005352301]	uncertain significance	9	6254501	6254501	Human		name
598180210	CV3972297	single nucleotide variant	NM_033439.4(IL33):c.355A>G (p.Ile119Val)	not specified [RCV005352302]	likely benign	9	6252877	6252877	Human		name
598180250	CV3972306	single nucleotide variant	NM_014440.3(IL36A):c.294A>T (p.Gln98His)	not specified [RCV005352308]	uncertain significance	2	113007861	113007861	Human		name
598207656	CV3972307	single nucleotide variant	NM_173178.3(IL36B):c.128T>C (p.Leu43Pro)	not specified [RCV005338007]	uncertain significance	2	113029072	113029072	Human		name
598180257	CV3972309	single nucleotide variant	NM_019618.4(IL36G):c.202G>A (p.Glu68Lys)	not specified [RCV005352309]	uncertain significance	2	112980050	112980050	Human		name
8604416	CV48520	single nucleotide variant	NM_012275.3(IL36RN):c.28C>T (p.Arg10Ter)	Acrodermatitis continua suppurativa of Hallopeau [RCV002508138]\|Generalized pustular psoriasis [RCV000033134]	pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	2	113059466	113059466	Human	1	name
13619073	CV516296	single nucleotide variant	NM_012275.3(IL36RN):c.369G>C (p.Thr123=)	Autoinflammatory syndrome [RCV002263870]\|Generalized pustular psoriasis [RCV000635397]\|not provided [RCV004710170]	benign\|likely benign	2	113062578	113062578	Human	2	name
13619076	CV516336	single nucleotide variant	NM_012275.3(IL36RN):c.411C>T (p.Pro137=)	Generalized pustular psoriasis [RCV001405968]	likely benign	2	113062620	113062620	Human	1	name
15156117	CV696981	single nucleotide variant	NM_014439.4(IL37):c.454C>T (p.Arg152Trp)	not provided [RCV000946631]	benign	2	112918606	112918606	Human		name
15198260	CV701027	single nucleotide variant	NM_033439.4(IL33):c.789C>G (p.Ile263Met)	not provided [RCV000956701]	benign	9	6256144	6256144	Human		name
15134266	CV711996	single nucleotide variant	NM_033439.4(IL33):c.457G>T (p.Asp153Tyr)	not provided [RCV000965097]	benign	9	6252979	6252979	Human		name
15184820	CV711997	single nucleotide variant	NM_033439.4(IL33):c.603C>G (p.His201Gln)	not provided [RCV000975205]	benign	9	6254544	6254544	Human		name
15154368	CV714870	single nucleotide variant	NM_001376923.1(IL32):c.16G>A (p.Val6Ile)	not provided [RCV000968724]	benign	16	3067377	3067377	Human		name
15157791	CV714871	single nucleotide variant	NM_001376923.1(IL32):c.123G>A (p.Ser41=)	not provided [RCV000969375]	benign	16	3067992	3067992	Human		name
15110200	CV721481	single nucleotide variant	NM_139017.7(IL31RA):c.432A>G (p.Thr144=)	not provided [RCV000894014]	benign	5	55872429	55872429	Human		name
15169000	CV721482	single nucleotide variant	NM_139017.7(IL31RA):c.708G>A (p.Ala236=)	not provided [RCV000883178]	benign	5	55890071	55890071	Human		name
15163100	CV726592	single nucleotide variant	NM_001376923.1(IL32):c.201A>G (p.Pro67=)	not provided [RCV000881895]	benign	16	3068239	3068239	Human		name
15171434	CV743509	single nucleotide variant	NM_002183.4(IL3RA):c.1098G>A (p.Glu366=)	not provided [RCV000905468]	benign	X	1382426	1382426	Human		name
15171434	CV743509	single nucleotide variant	NM_002183.4(IL3RA):c.1098G>A (p.Glu366=)	not provided [RCV000905468]	benign	Y	1382426	1382426	Human		name
15152379	CV758687	single nucleotide variant	NM_002183.4(IL3RA):c.257C>T (p.Ala86Val)	not provided [RCV000923860]	likely benign	X	1348504	1348504	Human		name
15152379	CV758687	single nucleotide variant	NM_002183.4(IL3RA):c.257C>T (p.Ala86Val)	not provided [RCV000923860]	likely benign	Y	1348504	1348504	Human		name
15197828	CV762161	single nucleotide variant	NM_012275.3(IL36RN):c.306G>A (p.Arg102=)	Generalized pustular psoriasis [RCV000934625]	likely benign	2	113062515	113062515	Human	1	name
8629794	CV84941	single nucleotide variant	NM_014438.4(IL36B):c.169G>A (p.Glu57Lys)	Malignant melanoma [RCV000065023]	not provided	2	113029031	113029031	Human		name
8629797	CV84944	single nucleotide variant	NM_012275.3(IL36RN):c.333C>T (p.Phe111=)	Generalized pustular psoriasis [RCV000370369]	conflicting interpretations of pathogenicity\|uncertain significance\|not provided	2	113062542	113062542	Human	1	name
8634545	CV89765	single nucleotide variant	NM_001014336.1(IL31):c.195C>T (p.Ser65=)	Malignant melanoma [RCV000069862]	not provided	12	122172712	122172712	Human		name
38477520	CV930790	single nucleotide variant	NM_012275.3(IL36RN):c.369G>A (p.Thr123=)	Autoinflammatory syndrome [RCV002264220]\|Generalized pustular psoriasis [RCV001205120]	likely benign\|uncertain significance	2	113062578	113062578	Human	2	name
126734305	CV1023673	single nucleotide variant	NM_012275.3(IL36RN):c.194G>A (p.Ser65Asn)	Generalized pustular psoriasis [RCV001349918]	uncertain significance	2	113062202	113062202	Human	1	name
126917398	CV1040510	single nucleotide variant	NM_012275.3(IL36RN):c.139A>G (p.Asn47Asp)	Generalized pustular psoriasis [RCV001361143]	uncertain significance	2	113062147	113062147	Human	1	name
126908023	CV1040511	single nucleotide variant	NM_012275.3(IL36RN):c.266A>G (p.Tyr89Cys)	Acrodermatitis continua suppurativa of Hallopeau [RCV002476678]\|Generalized pustular psoriasis [RCV001367500]	uncertain significance	2	113062475	113062475	Human	1	name
151765747	CV1358906	single nucleotide variant	NM_012275.3(IL36RN):c.253A>G (p.Ile85Val)	Generalized pustular psoriasis [RCV001970678]	uncertain significance	2	113062462	113062462	Human	1	name
151746694	CV1402917	single nucleotide variant	NM_012275.3(IL36RN):c.208T>C (p.Cys70Arg)	Generalized pustular psoriasis [RCV001912507]	uncertain significance	2	113062216	113062216	Human	1	name
151751464	CV1426737	deletion	NM_012275.3(IL36RN):c.329del (p.Ser110fs)	Generalized pustular psoriasis [RCV002006904]	uncertain significance	2	113062538	113062538	Human	1	name
151773586	CV1430590	duplication	NM_012275.3(IL36RN):c.335dup (p.Ser113fs)	Generalized pustular psoriasis [RCV001864306]	uncertain significance	2	113062543	113062544	Human	1	name
151869896	CV1454026	single nucleotide variant	NM_012275.3(IL36RN):c.188G>T (p.Gly63Val)	Generalized pustular psoriasis [RCV001925062]\|Inborn genetic diseases [RCV004631810]	uncertain significance	2	113062196	113062196	Human	2	name
153305905	CV1686721	single nucleotide variant	NM_012275.3(IL36RN):c.277A>G (p.Lys93Glu)	Autoinflammatory syndrome [RCV002264632]\|Generalized pustular psoriasis [RCV003095934]	uncertain significance	2	113062486	113062486	Human	2	name
9684842	CV170217	single nucleotide variant	NM_012275.3(IL36RN):c.104A>G (p.Lys35Arg)	Acrodermatitis continua suppurativa of Hallopeau [RCV002508141]\|Generalized pustular psoriasis [RCV000148040]	pathogenic\|uncertain significance\|not provided	2	113060926	113060926	Human	1	name
155675104	CV1771685	single nucleotide variant	NM_012275.3(IL36RN):c.140A>T (p.Asn47Ile)	Generalized pustular psoriasis [RCV002297734]	uncertain significance	2	113062148	113062148	Human	1	name
156393067	CV1933782	single nucleotide variant	NM_012275.3(IL36RN):c.130G>T (p.Val44Leu)	Generalized pustular psoriasis [RCV002654572]	uncertain significance	2	113062138	113062138	Human	1	name
156095378	CV2050839	single nucleotide variant	NM_012275.3(IL36RN):c.291C>A (p.Ser97Arg)	Generalized pustular psoriasis [RCV002824348]	uncertain significance	2	113062500	113062500	Human	1	name
156173417	CV2051736	single nucleotide variant	NM_012275.3(IL36RN):c.123G>C (p.Glu41Asp)	Generalized pustular psoriasis [RCV002828060]	uncertain significance	2	113062131	113062131	Human	1	name
156180898	CV2201776	single nucleotide variant	NM_001376923.1(IL32):c.68A>G (p.Glu23Gly)	not specified [RCV004082217]	uncertain significance	16	3067567	3067567	Human		name
156084188	CV2205572	single nucleotide variant	NM_014440.3(IL36A):c.322T>A (p.Tyr108Asn)	not specified [RCV004082496]	uncertain significance	2	113007889	113007889	Human		name
155965085	CV2206328	single nucleotide variant	NM_001376923.1(IL32):c.76T>C (p.Tyr26His)	not specified [RCV004078665]	uncertain significance	16	3067575	3067575	Human		name
156375812	CV2210318	single nucleotide variant	NM_012275.3(IL36RN):c.215T>G (p.Val72Gly)	Inborn genetic diseases [RCV002677689]	uncertain significance	2	113062223	113062223	Human	1	name
156049513	CV2315859	single nucleotide variant	NM_014438.5(IL36B):c.464G>A (p.Arg155Gln)	not specified [RCV004171636]	uncertain significance	2	113022705	113022705	Human		name
329383044	CV2441735	single nucleotide variant	NM_014440.3(IL36A):c.446C>T (p.Thr149Ile)	not specified [RCV004259903]	uncertain significance	2	113008013	113008013	Human		name
329391526	CV2448660	single nucleotide variant	NM_014438.5(IL36B):c.467C>T (p.Thr156Ile)	not specified [RCV004259329]	uncertain significance	2	113022702	113022702	Human		name
401746473	CV2694864	single nucleotide variant	NM_014440.3(IL36A):c.453C>A (p.Asp151Glu)	not specified [RCV004300938]	uncertain significance	2	113008020	113008020	Human		name
401735637	CV2695364	single nucleotide variant	NM_019618.4(IL36G):c.361C>T (p.Arg121Cys)	not specified [RCV004305575]	uncertain significance	2	112984900	112984900	Human		name
11652650	CV282256	single nucleotide variant	NM_012275.3(IL36RN):c.248T>A (p.Val83Glu)	Generalized pustular psoriasis [RCV000306409]\|Inborn genetic diseases [RCV002521265]	uncertain significance	2	113062457	113062457	Human	2	name
405193246	CV2940183	single nucleotide variant	NM_012275.3(IL36RN):c.184C>T (p.Gln62Ter)	Generalized pustular psoriasis [RCV003641134]	pathogenic	2	113062192	113062192	Human	1	name
405195012	CV2966875	single nucleotide variant	NM_012275.3(IL36RN):c.215T>C (p.Val72Ala)	Generalized pustular psoriasis [RCV003641342]	uncertain significance	2	113062223	113062223	Human	1	name
405804942	CV3271189	single nucleotide variant	NM_001014336.2(IL31):c.85G>A (p.Val29Ile)	not specified [RCV004405250]	likely benign	12	122173924	122173924	Human		name
405804944	CV3271190	single nucleotide variant	NM_139017.7(IL31RA):c.115C>G (p.Leu39Val)	not specified [RCV004405251]	uncertain significance	5	55859560	55859560	Human		name
405804958	CV3271198	single nucleotide variant	NM_139017.7(IL31RA):c.236A>G (p.Glu79Gly)	not specified [RCV004405259]	uncertain significance	5	55868872	55868872	Human		name
405804987	CV3271214	single nucleotide variant	NM_014440.3(IL36A):c.355G>C (p.Glu119Gln)	not specified [RCV004405275]	uncertain significance	2	113007922	113007922	Human		name
405804994	CV3271218	single nucleotide variant	NM_019618.4(IL36G):c.340G>A (p.Val114Met)	not specified [RCV004405279]	uncertain significance	2	112984879	112984879	Human		name
405804998	CV3271220	single nucleotide variant	NM_019618.4(IL36G):c.419T>C (p.Ile140Thr)	not specified [RCV004405281]	uncertain significance	2	112984958	112984958	Human		name
408377908	CV3500868	single nucleotide variant	NM_139017.7(IL31RA):c.2022C>T (p.Cys674=)	not provided [RCV004722518]	likely benign	5	55916847	55916847	Human		name
597656541	CV3552345	single nucleotide variant	NM_012275.3(IL36RN):c.179G>T (p.Gly60Val)	Acrodermatitis continua suppurativa of Hallopeau [RCV004821203]	uncertain significance	2	113062187	113062187	Human	1	name
597695595	CV3686522	single nucleotide variant	NM_001014336.2(IL31):c.89G>A (p.Arg30His)	not specified [RCV004929203]	likely benign	12	122173920	122173920	Human		name
597695606	CV3686523	single nucleotide variant	NM_001014336.2(IL31):c.47G>A (p.Cys16Tyr)	not specified [RCV004929204]	uncertain significance	12	122173962	122173962	Human		name
597774945	CV3686549	single nucleotide variant	NM_001393494.1(IL34):c.76A>G (p.Met26Val)	not specified [RCV004929230]	likely benign	16	70654585	70654585	Human		name
597774955	CV3686552	single nucleotide variant	NM_014440.3(IL36A):c.340A>G (p.Arg114Gly)	not specified [RCV004929233]	uncertain significance	2	113007907	113007907	Human		name
597774959	CV3686553	single nucleotide variant	NM_014440.3(IL36A):c.449C>G (p.Thr150Ser)	not specified [RCV004929234]	uncertain significance	2	113008016	113008016	Human		name
597695617	CV3686555	single nucleotide variant	NM_014438.5(IL36B):c.485G>C (p.Gly162Ala)	not specified [RCV004929236]	uncertain significance	2	113022684	113022684	Human		name
597695628	CV3686556	single nucleotide variant	NM_014438.5(IL36B):c.455C>T (p.Ser152Leu)	not specified [RCV004929237]	uncertain significance	2	113022714	113022714	Human		name
597774974	CV3686559	single nucleotide variant	NM_019618.4(IL36G):c.455C>A (p.Thr152Asn)	not specified [RCV004929240]	uncertain significance	2	112984994	112984994	Human		name
597848220	CV3823999	single nucleotide variant	NM_012275.3(IL36RN):c.164C>G (p.Ser55Cys)	Generalized pustular psoriasis [RCV005173238]	uncertain significance	2	113062172	113062172	Human	1	name
598207577	CV3972272	single nucleotide variant	NM_001014336.2(IL31):c.77C>T (p.Thr26Met)	not specified [RCV005337996]	uncertain significance	12	122173932	122173932	Human		name
598180116	CV3972278	single nucleotide variant	NM_139017.7(IL31RA):c.274G>A (p.Ala92Thr)	not specified [RCV005352288]	uncertain significance	5	55872271	55872271	Human		name
598207650	CV3972305	single nucleotide variant	NM_014440.3(IL36A):c.298G>C (p.Glu100Gln)	not specified [RCV005338006]	uncertain significance	2	113007865	113007865	Human		name
598207663	CV3972308	single nucleotide variant	NM_019618.4(IL36G):c.407C>T (p.Pro136Leu)	not specified [RCV005338008]	uncertain significance	2	112984946	112984946	Human		name
13519063	CV486247	single nucleotide variant	NM_012275.3(IL36RN):c.169G>A (p.Val57Ile)	Autoinflammatory syndrome [RCV002263818]\|Generalized pustular psoriasis [RCV001084574]\|not provided [RCV000585337]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	2	113062177	113062177	Human	2	name
13619065	CV516311	single nucleotide variant	NM_012275.3(IL36RN):c.200G>T (p.Cys67Phe)	Generalized pustular psoriasis [RCV000635392]	uncertain significance	2	113062208	113062208	Human	1	name
13619072	CV516323	single nucleotide variant	NM_012275.3(IL36RN):c.140A>G (p.Asn47Ser)	Acrodermatitis continua suppurativa of Hallopeau [RCV002492978]\|Autoinflammatory syndrome [RCV002263869]\|Generalized pustular psoriasis [RCV000635396]\|not provided [RCV001637107]	benign\|likely benign	2	113062148	113062148	Human	2	name
13619068	CV516324	single nucleotide variant	NM_012275.3(IL36RN):c.230C>T (p.Thr77Ile)	Autoinflammatory syndrome [RCV002263868]\|Generalized pustular psoriasis [RCV000635394]\|not provided [RCV001200639]	uncertain significance	2	113062238	113062238	Human	2	name
13822563	CV559182	single nucleotide variant	NM_012275.3(IL36RN):c.227C>T (p.Pro76Leu)	Acrodermatitis continua suppurativa of Hallopeau [RCV004796284]\|Generalized pustular psoriasis [RCV000697421]\|not provided [RCV000997194]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	2	113062235	113062235	Human	1	name
14699203	CV624197	single nucleotide variant	NM_012275.3(IL36RN):c.101G>C (p.Gly34Ala)	not provided [RCV000788467]	uncertain significance	2	113060923	113060923	Human		name
14713167	CV628413	single nucleotide variant	NM_012275.3(IL36RN):c.136C>T (p.Pro46Ser)	Generalized pustular psoriasis [RCV000792408]\|not provided [RCV003480821]	uncertain significance	2	113062144	113062144	Human	1	name
14714696	CV628414	single nucleotide variant	NM_012275.3(IL36RN):c.164C>T (p.Ser55Phe)	Generalized pustular psoriasis [RCV000797722]	uncertain significance	2	113062172	113062172	Human	1	name
15200543	CV703636	single nucleotide variant	NM_001376923.1(IL32):c.64A>C (p.Ile22Leu)	not provided [RCV000957361]	benign	16	3067563	3067563	Human		name
15200546	CV703637	single nucleotide variant	NM_001376923.1(IL32):c.70A>G (p.Arg24Gly)	not provided [RCV000957362]	benign	16	3067569	3067569	Human		name
15200550	CV703638	single nucleotide variant	NM_001376923.1(IL32):c.77A>G (p.Tyr26Cys)	not provided [RCV000957363]	benign	16	3067576	3067576	Human		name
15172452	CV706341	single nucleotide variant	NM_002183.4(IL3RA):c.368G>C (p.Ser123Thr)	not provided [RCV000950029]	likely benign	X	1352169	1352169	Human		name
15172452	CV706341	single nucleotide variant	NM_002183.4(IL3RA):c.368G>C (p.Ser123Thr)	not provided [RCV000950029]	likely benign	Y	1352169	1352169	Human		name
15145143	CV709948	single nucleotide variant	NM_139017.7(IL31RA):c.131C>T (p.Ser44Leu)	not provided [RCV000966945]	benign	5	55859576	55859576	Human		name
15156325	CV715040	single nucleotide variant	NM_001393494.1(IL34):c.609C>T (p.Pro203=)	not provided [RCV000969091]	benign	16	70660067	70660067	Human		name
15186764	CV726768	single nucleotide variant	NM_001393494.1(IL34):c.462A>G (p.Pro154=)	not provided [RCV000887064]	benign	16	70659677	70659677	Human		name
15180374	CV732719	single nucleotide variant	NM_012275.3(IL36RN):c.245C>T (p.Pro82Leu)	Autoinflammatory syndrome [RCV002264077]\|Generalized pustular psoriasis [RCV000907339]	benign\|likely benign\|uncertain significance	2	113062454	113062454	Human	2	name
15186152	CV740330	single nucleotide variant	NM_001393494.1(IL34):c.47G>C (p.Gly16Ala)	not provided [RCV000908729]	likely benign	16	70654556	70654556	Human		name
15195369	CV765154	single nucleotide variant	NM_139017.7(IL31RA):c.1233G>C (p.Thr411=)	not provided [RCV000933919]	likely benign	5	55906269	55906269	Human		name
26913807	CV824716	single nucleotide variant	NM_012275.3(IL36RN):c.130G>A (p.Val44Met)	Generalized pustular psoriasis [RCV001036551]	uncertain significance	2	113062138	113062138	Human	1	name
26915360	CV824717	single nucleotide variant	NM_012275.3(IL36RN):c.275C>T (p.Ala92Val)	Generalized pustular psoriasis [RCV001038906]	uncertain significance	2	113062484	113062484	Human	1	name
38472475	CV930789	single nucleotide variant	NM_012275.3(IL36RN):c.123G>T (p.Glu41Asp)	Generalized pustular psoriasis [RCV001203186]	uncertain significance	2	113062131	113062131	Human	1	name
126745297	CV1003175	single nucleotide variant	NM_012275.3(IL36RN):c.302A>T (p.Tyr101Phe)	Generalized pustular psoriasis [RCV001325905]	uncertain significance	2	113062511	113062511	Human	1	name
126744318	CV1015821	single nucleotide variant	NM_012275.3(IL36RN):c.334G>T (p.Glu112Ter)	Pustular psoriasis, generalized [RCV001330412]	pathogenic	2	113062543	113062543	Human		name
126730759	CV1020111	deletion	NM_139017.7(IL31RA):c.1783del (p.Ser595fs)	Amyloidosis, primary localized cutaneous, 2 [RCV001333525]	pathogenic	5	55914891	55914891	Human		name
126923812	CV1040512	single nucleotide variant	NM_012275.3(IL36RN):c.451T>A (p.Phe151Ile)	Autoinflammatory syndrome [RCV002264283]\|Generalized pustular psoriasis [RCV001366279]	uncertain significance	2	113062660	113062660	Human	2	name
151766386	CV1348588	single nucleotide variant	NM_012275.3(IL36RN):c.317G>C (p.Gly106Ala)	Autoinflammatory syndrome [RCV002264413]\|Generalized pustular psoriasis [RCV001895901]	uncertain significance	2	113062526	113062526	Human	2	name
151735238	CV1354680	single nucleotide variant	NM_012275.3(IL36RN):c.418G>T (p.Gly140Cys)	Generalized pustular psoriasis [RCV001892677]	uncertain significance	2	113062627	113062627	Human	1	name
151790454	CV1373505	single nucleotide variant	NM_012275.3(IL36RN):c.422G>A (p.Gly141Asp)	Generalized pustular psoriasis [RCV001898127]	uncertain significance	2	113062631	113062631	Human	1	name
151892901	CV1411606	single nucleotide variant	NM_012275.3(IL36RN):c.308G>A (p.Arg103Gln)	Autoinflammatory syndrome [RCV002264409]\|Generalized pustular psoriasis [RCV001944592]	uncertain significance	2	113062517	113062517	Human	2	name
151756684	CV1414307	single nucleotide variant	NM_012275.3(IL36RN):c.458A>G (p.Gln153Arg)	Generalized pustular psoriasis [RCV001894863]	uncertain significance	2	113062667	113062667	Human	1	name
9684843	CV170218	single nucleotide variant	NM_012275.3(IL36RN):c.304C>T (p.Arg102Trp)	Acrodermatitis continua suppurativa of Hallopeau [RCV002492539]\|not provided [RCV001200640]	pathogenic\|uncertain significance\|not provided	2	113062513	113062513	Human	1	name
156101918	CV1907165	single nucleotide variant	NM_012275.3(IL36RN):c.305G>A (p.Arg102Gln)	Generalized pustular psoriasis [RCV003080633]	uncertain significance	2	113062514	113062514	Human	1	name
156396051	CV1924729	single nucleotide variant	NM_012275.3(IL36RN):c.418G>A (p.Gly140Ser)	Generalized pustular psoriasis [RCV002654918]	uncertain significance	2	113062627	113062627	Human	1	name
156389031	CV1955144	single nucleotide variant	NM_012275.3(IL36RN):c.350C>A (p.Pro117Gln)	Generalized pustular psoriasis [RCV002583708]	uncertain significance	2	113062559	113062559	Human	1	name
156340655	CV2174834	single nucleotide variant	NM_012275.3(IL36RN):c.322A>T (p.Thr108Ser)	Generalized pustular psoriasis [RCV003047718]	uncertain significance	2	113062531	113062531	Human	1	name
156292374	CV2233446	single nucleotide variant	NM_001014336.2(IL31):c.297C>A (p.Asp99Glu)	not specified [RCV004106072]	uncertain significance	12	122172610	122172610	Human		name
156056695	CV2243329	single nucleotide variant	NM_001376923.1(IL32):c.128T>C (p.Leu43Pro)	not specified [RCV004112026]	uncertain significance	16	3067997	3067997	Human		name
155966862	CV2261099	single nucleotide variant	NM_001376923.1(IL32):c.135G>C (p.Glu45Asp)	not specified [RCV004128002]	uncertain significance	16	3068004	3068004	Human		name
156251493	CV2286848	single nucleotide variant	NM_139017.7(IL31RA):c.401A>T (p.Asn134Ile)	not specified [RCV004142649]	uncertain significance	5	55872398	55872398	Human		name
156189694	CV2289200	single nucleotide variant	NM_001014336.2(IL31):c.101C>G (p.Pro34Arg)	not specified [RCV004152201]	uncertain significance	12	122173908	122173908	Human		name
156267227	CV2296581	single nucleotide variant	NM_139017.7(IL31RA):c.830G>A (p.Arg277Lys)	not specified [RCV004154648]	uncertain significance	5	55896407	55896407	Human		name
156055622	CV2343410	single nucleotide variant	NM_001393494.1(IL34):c.288G>C (p.Leu96Phe)	not specified [RCV004197489]	uncertain significance	16	70657007	70657007	Human		name
156309224	CV2366545	single nucleotide variant	NM_139017.7(IL31RA):c.427A>G (p.Met143Val)	not specified [RCV004208519]	uncertain significance	5	55872424	55872424	Human		name
155982706	CV2371144	single nucleotide variant	NM_139017.7(IL31RA):c.574C>T (p.Leu192Phe)	not specified [RCV004220892]	uncertain significance	5	55883163	55883163	Human		name
156091387	CV2389453	single nucleotide variant	NM_012275.3(IL36RN):c.313A>G (p.Met105Val)	Inborn genetic diseases [RCV002784334]\|not provided [RCV003481443]	uncertain significance	2	113062522	113062522	Human	1	name
329360776	CV2462957	single nucleotide variant	NM_139017.7(IL31RA):c.547C>T (p.Pro183Ser)	not specified [RCV004272792]	uncertain significance	5	55883136	55883136	Human		name
329376507	CV2472099	single nucleotide variant	NM_001393494.1(IL34):c.149G>A (p.Arg50Gln)	not specified [RCV004283235]	uncertain significance	16	70654658	70654658	Human		name
401743936	CV2696902	single nucleotide variant	NM_139017.7(IL31RA):c.818C>T (p.Ala273Val)	not specified [RCV004292906]	likely benign	5	55896395	55896395	Human		name
401742891	CV2715344	single nucleotide variant	NM_001376923.1(IL32):c.208A>G (p.Thr70Ala)	not specified [RCV004324676]	uncertain significance	16	3068996	3068996	Human		name
401763847	CV2725327	single nucleotide variant	NM_139017.7(IL31RA):c.735C>A (p.Asp245Glu)	not specified [RCV004319987]	uncertain significance	5	55890098	55890098	Human		name
401748980	CV2727763	single nucleotide variant	NM_001014336.2(IL31):c.293T>C (p.Leu98Pro)	not specified [RCV004323794]	uncertain significance	12	122172614	122172614	Human		name
401778683	CV2735453	single nucleotide variant	NM_001393494.1(IL34):c.223G>A (p.Ala75Thr)	not specified [RCV004331012]	uncertain significance	16	70656662	70656662	Human		name
401828314	CV2744677	single nucleotide variant	NM_012275.3(IL36RN):c.338C>A (p.Ser113Ter)	Acrodermatitis continua suppurativa of Hallopeau [RCV003328076]	likely pathogenic	2	113062547	113062547	Human	1	name
401856923	CV2769528	single nucleotide variant	NM_001014336.2(IL31):c.202T>C (p.Tyr68His)	not specified [RCV004351185]	uncertain significance	12	122172705	122172705	Human		name
401871865	CV2783621	single nucleotide variant	NM_001376923.1(IL32):c.185A>C (p.Tyr62Ser)	not specified [RCV004365936]	uncertain significance	16	3068223	3068223	Human		name
401879125	CV2790976	single nucleotide variant	NM_001393494.1(IL34):c.101A>G (p.Glu34Gly)	not specified [RCV004354601]	uncertain significance	16	70654610	70654610	Human		name
405804931	CV3271183	single nucleotide variant	NM_001014336.2(IL31):c.104G>A (p.Ser35Asn)	not specified [RCV004405244]	uncertain significance	12	122173905	122173905	Human		name
405804933	CV3271184	single nucleotide variant	NM_001014336.2(IL31):c.163G>A (p.Asp55Asn)	not specified [RCV004405245]	uncertain significance	12	122173846	122173846	Human		name
405804960	CV3271199	single nucleotide variant	NM_139017.7(IL31RA):c.818C>A (p.Ala273Glu)	not specified [RCV004405260]	uncertain significance	5	55896395	55896395	Human		name
405804962	CV3271200	single nucleotide variant	NM_001376923.1(IL32):c.106C>T (p.Arg36Cys)	not specified [RCV004405261]	uncertain significance	16	3067605	3067605	Human		name
405805000	CV3271221	single nucleotide variant	NM_012275.3(IL36RN):c.434C>T (p.Pro145Leu)	Inborn genetic diseases [RCV004405282]	uncertain significance	2	113062643	113062643	Human	1	name
407516007	CV3444610	single nucleotide variant	NM_139017.7(IL31RA):c.662C>T (p.Thr221Met)	not specified [RCV004628056]	likely benign	5	55890025	55890025	Human		name
407511215	CV3444611	single nucleotide variant	NM_139017.7(IL31RA):c.590T>A (p.Val197Asp)	not specified [RCV004626390]	uncertain significance	5	55883179	55883179	Human		name
407516010	CV3444612	single nucleotide variant	NM_139017.7(IL31RA):c.752T>C (p.Met251Thr)	not specified [RCV004628057]	uncertain significance	5	55890115	55890115	Human		name
407516014	CV3444613	single nucleotide variant	NM_139017.7(IL31RA):c.971A>G (p.His324Arg)	not specified [RCV004628058]	uncertain significance	5	55900034	55900034	Human		name
407516021	CV3444615	single nucleotide variant	NM_001376923.1(IL32):c.156G>C (p.Glu52Asp)	not specified [RCV004628060]	uncertain significance	16	3068194	3068194	Human		name
407516035	CV3444618	single nucleotide variant	NM_001393494.1(IL34):c.262C>T (p.Arg88Trp)	not specified [RCV004628063]	uncertain significance	16	70656981	70656981	Human		name
597774857	CV3686526	single nucleotide variant	NM_139017.7(IL31RA):c.839G>A (p.Arg280Gln)	not specified [RCV004929207]	likely benign	5	55896416	55896416	Human		name
597774864	CV3686528	single nucleotide variant	NM_139017.7(IL31RA):c.778T>C (p.Cys260Arg)	not specified [RCV004929209]	uncertain significance	5	55896355	55896355	Human		name
597774877	CV3686531	single nucleotide variant	NM_139017.7(IL31RA):c.942G>C (p.Met314Ile)	not specified [RCV004929212]	uncertain significance	5	55900005	55900005	Human		name
597774889	CV3686534	single nucleotide variant	NM_001376923.1(IL32):c.136C>G (p.Leu46Val)	not specified [RCV004929215]	uncertain significance	16	3068005	3068005	Human		name
597774893	CV3686535	single nucleotide variant	NM_001376923.1(IL32):c.137T>G (p.Leu46Arg)	not specified [RCV004929216]	uncertain significance	16	3068006	3068006	Human		name
597774929	CV3686545	single nucleotide variant	NM_001393494.1(IL34):c.118T>G (p.Phe40Val)	not specified [RCV004929226]	uncertain significance	16	70654627	70654627	Human		name
597774933	CV3686546	single nucleotide variant	NM_001393494.1(IL34):c.119T>G (p.Phe40Cys)	not specified [RCV004929227]	uncertain significance	16	70654628	70654628	Human		name
597774937	CV3686547	single nucleotide variant	NM_001393494.1(IL34):c.120T>G (p.Phe40Leu)	not specified [RCV004929228]	uncertain significance	16	70654629	70654629	Human		name
597774948	CV3686550	single nucleotide variant	NM_001393494.1(IL34):c.205G>A (p.Glu69Lys)	not specified [RCV004929231]	uncertain significance	16	70656644	70656644	Human		name
598180099	CV3972273	single nucleotide variant	NM_001014336.2(IL31):c.131A>G (p.Glu44Gly)	not specified [RCV005352285]	uncertain significance	12	122173878	122173878	Human		name
598207583	CV3972274	single nucleotide variant	NM_001014336.2(IL31):c.106G>A (p.Asp36Asn)	not specified [RCV005337997]	uncertain significance	12	122173903	122173903	Human		name
598180103	CV3972275	single nucleotide variant	NM_139017.7(IL31RA):c.685T>A (p.Tyr229Asn)	not specified [RCV005352286]	uncertain significance	5	55890048	55890048	Human		name
598207588	CV3972277	single nucleotide variant	NM_139017.7(IL31RA):c.410G>T (p.Gly137Val)	not specified [RCV005337998]	uncertain significance	5	55872407	55872407	Human		name
598207596	CV3972282	single nucleotide variant	NM_139017.7(IL31RA):c.979G>A (p.Gly327Ser)	not specified [RCV005337999]	uncertain significance	5	55900042	55900042	Human		name
598207611	CV3972285	single nucleotide variant	NM_001376923.1(IL32):c.251G>A (p.Gly84Asp)	not specified [RCV005338001]	uncertain significance	16	3069039	3069039	Human		name
8604415	CV48519	single nucleotide variant	NM_012275.3(IL36RN):c.368C>G (p.Thr123Arg)	Acrodermatitis continua suppurativa of Hallopeau [RCV002508137]	pathogenic	2	113062577	113062577	Human	1	name
13619070	CV516298	single nucleotide variant	NM_012275.3(IL36RN):c.436A>G (p.Ile146Val)	Deficiency of the interleukin-36 receptor antagonist [RCV003330854]\|Generalized pustular psoriasis [RCV000635395]\|not provided [RCV004791652]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance\|not provided	2	113062645	113062645	Human	1	name
13619066	CV516327	single nucleotide variant	NM_012275.3(IL36RN):c.386A>G (p.Gln129Arg)	Generalized pustular psoriasis [RCV000635393]	uncertain significance	2	113062595	113062595	Human	1	name
14701881	CV628415	single nucleotide variant	NM_012275.3(IL36RN):c.368C>T (p.Thr123Met)	Generalized pustular psoriasis [RCV000820040]	uncertain significance	2	113062577	113062577	Human	1	name
15185585	CV703639	single nucleotide variant	NM_001376923.1(IL32):c.200C>T (p.Pro67Leu)	not provided [RCV000953026]	benign	16	3068238	3068238	Human	2	name
15185585	CV703639	single nucleotide variant	NM_001376923.1(IL32):c.200C>T (p.Pro67Leu)	not provided [RCV000953026]	benign	16	3068238	3068239	Human	2	name
15163095	CV726591	single nucleotide variant	NM_001376923.1(IL32):c.107G>A (p.Arg36His)	not provided [RCV000881894]	likely benign	16	3067606	3067606	Human	1	name
15163095	CV726591	single nucleotide variant	NM_001376923.1(IL32):c.107G>A (p.Arg36His)	not provided [RCV000881894]	likely benign	16	3067606	3067607	Human	1	name
8625106	CV80225	single nucleotide variant	NM_012275.3(IL36RN):c.334G>A (p.Glu112Lys)	Generalized pustular psoriasis [RCV001934777]	uncertain significance\|not provided	2	113062543	113062543	Human	1	name
26920605	CV824718	single nucleotide variant	NM_012275.3(IL36RN):c.307C>T (p.Arg103Trp)	Autoinflammatory syndrome [RCV002264160]\|Generalized pustular psoriasis [RCV001048048]	uncertain significance	2	113062516	113062516	Human	2	name
26921409	CV824719	single nucleotide variant	NM_012275.3(IL36RN):c.350C>T (p.Pro117Leu)	Generalized pustular psoriasis [RCV001049860]	uncertain significance	2	113062559	113062559	Human	1	name
8627859	CV83003	single nucleotide variant	NM_001172771.1(IL34):c.176C>T (p.Pro59Leu)	Malignant melanoma [RCV000063083]	not provided	16	70656615	70656615	Human		name
28872030	CV880862	single nucleotide variant	NM_012275.3(IL36RN):c.421G>A (p.Gly141Ser)	Generalized pustular psoriasis [RCV001132076]	uncertain significance	2	113062630	113062630	Human	1	name
126744803	CV987913	single nucleotide variant	NM_012275.3(IL36RN):c.349C>G (p.Pro117Ala)	Generalized pustular psoriasis [RCV001307839]\|Inborn genetic diseases [RCV004034145]	uncertain significance	2	113062558	113062558	Human	2	name
156378072	CV2207625	single nucleotide variant	NM_139017.7(IL31RA):c.1693A>C (p.Ile565Leu)	not specified [RCV004090404]	uncertain significance	5	55913527	55913527	Human		name
156240330	CV2221328	single nucleotide variant	NM_139017.7(IL31RA):c.1401G>T (p.Lys467Asn)	not specified [RCV004094751]	uncertain significance	5	55908311	55908311	Human		name
156242893	CV2231466	single nucleotide variant	NM_139017.7(IL31RA):c.1174T>C (p.Phe392Leu)	not specified [RCV004096538]	uncertain significance	5	55906210	55906210	Human		name
156228839	CV2234927	single nucleotide variant	NM_001014336.2(IL31):c.376G>A (p.Val126Met)	not specified [RCV004113131]	uncertain significance	12	122172531	122172531	Human		name
155984981	CV2241179	single nucleotide variant	NM_139017.7(IL31RA):c.2269C>T (p.Pro757Ser)	not specified [RCV004104203]	uncertain significance	5	55917094	55917094	Human		name
156024265	CV2242109	single nucleotide variant	NM_139017.7(IL31RA):c.1939G>A (p.Val647Ile)	not specified [RCV004109329]	uncertain significance	5	55916764	55916764	Human		name
156243641	CV2242948	single nucleotide variant	NM_139017.7(IL31RA):c.1940T>C (p.Val647Ala)	not specified [RCV004107833]	uncertain significance	5	55916765	55916765	Human		name
156037858	CV2259822	single nucleotide variant	NM_139017.7(IL31RA):c.1074T>G (p.Phe358Leu)	not specified [RCV004117087]	uncertain significance	5	55906110	55906110	Human		name
156172282	CV2286849	single nucleotide variant	NM_001376923.1(IL32):c.473T>C (p.Leu158Pro)	not specified [RCV004142650]	uncertain significance	16	3069261	3069261	Human		name
155999994	CV2287333	single nucleotide variant	NM_001376923.1(IL32):c.302G>T (p.Gly101Val)	not specified [RCV004146955]	uncertain significance	16	3069090	3069090	Human		name
156184041	CV2292202	single nucleotide variant	NM_001376923.1(IL32):c.516C>G (p.Asp172Glu)	not specified [RCV004148250]	uncertain significance	16	3069304	3069304	Human		name
155900768	CV2297992	single nucleotide variant	NM_001014336.2(IL31):c.319A>G (p.Ile107Val)	not specified [RCV004157908]	uncertain significance	12	122172588	122172588	Human		name
156178016	CV2298260	single nucleotide variant	NM_001393494.1(IL34):c.425T>C (p.Val142Ala)	not specified [RCV004160177]	uncertain significance	16	70659640	70659640	Human		name
156202224	CV2300615	single nucleotide variant	NM_001376923.1(IL32):c.326T>G (p.Met109Arg)	not specified [RCV004155573]	uncertain significance	16	3069114	3069114	Human		name
155903363	CV2301627	single nucleotide variant	NM_001393494.1(IL34):c.514A>T (p.Met172Leu)	not specified [RCV004162531]	uncertain significance	16	70659729	70659729	Human		name
156046616	CV2315623	single nucleotide variant	NM_001376923.1(IL32):c.457T>C (p.Cys153Arg)	not specified [RCV004169659]	uncertain significance	16	3069245	3069245	Human		name
156260753	CV2322323	single nucleotide variant	NM_139017.7(IL31RA):c.1156A>T (p.Thr386Ser)	not specified [RCV004176082]	uncertain significance	5	55906192	55906192	Human		name
155907627	CV2354462	single nucleotide variant	NM_139017.7(IL31RA):c.1232C>T (p.Thr411Met)	not specified [RCV004202452]	uncertain significance	5	55906268	55906268	Human		name
155906976	CV2357417	single nucleotide variant	NM_001014336.2(IL31):c.355G>A (p.Ala119Thr)	not specified [RCV004200296]	uncertain significance	12	122172552	122172552	Human		name
156104431	CV2360973	single nucleotide variant	NM_139017.7(IL31RA):c.1327T>A (p.Ser443Thr)	Amyloidosis, primary localized cutaneous, 2 [RCV005399222]\|not specified [RCV004216171]	uncertain significance	5	55907433	55907433	Human	1	name
329377622	CV2449869	single nucleotide variant	NM_001393494.1(IL34):c.433G>A (p.Val145Met)	not specified [RCV004268959]	uncertain significance	16	70659648	70659648	Human		name
329394628	CV2461456	single nucleotide variant	NM_001376923.1(IL32):c.298C>A (p.Pro100Thr)	not specified [RCV004267600]	uncertain significance	16	3069086	3069086	Human		name
329352900	CV2470621	single nucleotide variant	NM_139017.7(IL31RA):c.2107C>A (p.Leu703Ile)	not specified [RCV004273615]	uncertain significance	5	55916932	55916932	Human		name
401739116	CV2673226	single nucleotide variant	NM_139017.7(IL31RA):c.2143G>A (p.Ala715Thr)	Amyloidosis, primary localized cutaneous, 2 [RCV005399301]\|not specified [RCV004286033]	uncertain significance	5	55916968	55916968	Human	1	name
401719978	CV2675739	single nucleotide variant	NM_001376923.1(IL32):c.524A>G (p.Glu175Gly)	not specified [RCV004287985]	uncertain significance	16	3069312	3069312	Human		name
401765812	CV2717876	single nucleotide variant	NM_139017.7(IL31RA):c.2135G>A (p.Arg712His)	not specified [RCV004321847]	uncertain significance	5	55916960	55916960	Human		name
401876609	CV2761130	single nucleotide variant	NM_139017.7(IL31RA):c.2110C>T (p.Arg704Cys)	not specified [RCV004338785]	likely benign	5	55916935	55916935	Human		name
401880145	CV2766140	single nucleotide variant	NM_139017.7(IL31RA):c.1553G>A (p.Arg518Gln)	not specified [RCV004340592]	uncertain significance	5	55910583	55910583	Human		name
401861559	CV2779861	single nucleotide variant	NM_139017.7(IL31RA):c.1743G>T (p.Leu581Phe)	not specified [RCV004353480]	uncertain significance	5	55914853	55914853	Human		name
401870483	CV2792388	single nucleotide variant	NM_139017.7(IL31RA):c.2158C>T (p.Leu720Phe)	not specified [RCV004361551]	uncertain significance	5	55916983	55916983	Human		name
405804940	CV3271188	single nucleotide variant	NM_001014336.2(IL31):c.451G>A (p.Ala151Thr)	not specified [RCV004405249]	uncertain significance	12	122172456	122172456	Human		name
405804946	CV3271191	single nucleotide variant	NM_139017.7(IL31RA):c.1161G>C (p.Trp387Cys)	not specified [RCV004405252]	uncertain significance	5	55906197	55906197	Human		name
405804947	CV3271192	single nucleotide variant	NM_139017.7(IL31RA):c.1417T>G (p.Trp473Gly)	not specified [RCV004405253]	uncertain significance	5	55908327	55908327	Human		name
405804949	CV3271193	single nucleotide variant	NM_139017.7(IL31RA):c.1601G>A (p.Gly534Glu)	not specified [RCV004405254]	uncertain significance	5	55910631	55910631	Human		name
405804951	CV3271194	single nucleotide variant	NM_139017.7(IL31RA):c.2053A>G (p.Ser685Gly)	not specified [RCV004405255]	uncertain significance	5	55916878	55916878	Human		name
405804953	CV3271195	single nucleotide variant	NM_139017.7(IL31RA):c.2114C>G (p.Ser705Trp)	not specified [RCV004405256]	uncertain significance	5	55916939	55916939	Human		name
405804955	CV3271196	single nucleotide variant	NM_139017.7(IL31RA):c.2114C>T (p.Ser705Leu)	not specified [RCV004405257]	likely benign	5	55916939	55916939	Human		name
405804957	CV3271197	single nucleotide variant	NM_139017.7(IL31RA):c.2134C>T (p.Arg712Cys)	not specified [RCV004405258]	likely benign	5	55916959	55916959	Human		name
405804964	CV3271201	single nucleotide variant	NM_001376923.1(IL32):c.382G>C (p.Ala128Pro)	not specified [RCV004405262]	uncertain significance	16	3069170	3069170	Human		name
405804966	CV3271202	single nucleotide variant	NM_001376923.1(IL32):c.514G>A (p.Asp172Asn)	not specified [RCV004405263]	uncertain significance	16	3069302	3069302	Human		name
405804968	CV3271203	single nucleotide variant	NM_001376923.1(IL32):c.550C>T (p.Pro184Ser)	not specified [RCV004405264]	uncertain significance	16	3069338	3069338	Human		name
405804979	CV3271209	single nucleotide variant	NM_001393494.1(IL34):c.364G>A (p.Val122Met)	not specified [RCV004405270]	uncertain significance	16	70657083	70657083	Human		name
405804981	CV3271210	single nucleotide variant	NM_001393494.1(IL34):c.646C>T (p.Pro216Ser)	not specified [RCV004405271]	uncertain significance	16	70660104	70660104	Human		name
407483341	CV3444609	single nucleotide variant	NM_001014336.2(IL31):c.383C>T (p.Thr128Ile)	not specified [RCV004628055]	uncertain significance	12	122172524	122172524	Human		name
407516038	CV3444619	single nucleotide variant	NM_001393494.1(IL34):c.322G>A (p.Val108Met)	not specified [RCV004628064]	uncertain significance	16	70657041	70657041	Human		name
597774849	CV3686524	single nucleotide variant	NM_139017.7(IL31RA):c.1403C>T (p.Thr468Met)	not specified [RCV004929205]	uncertain significance	5	55908313	55908313	Human		name
597774853	CV3686525	single nucleotide variant	NM_139017.7(IL31RA):c.1303C>T (p.His435Tyr)	not specified [RCV004929206]	uncertain significance	5	55907409	55907409	Human		name
597774861	CV3686527	single nucleotide variant	NM_139017.7(IL31RA):c.2260G>C (p.Glu754Gln)	not specified [RCV004929208]	likely benign	5	55917085	55917085	Human		name
597774869	CV3686529	single nucleotide variant	NM_139017.7(IL31RA):c.1225C>A (p.Gln409Lys)	not specified [RCV004929210]	uncertain significance	5	55906261	55906261	Human		name
597774873	CV3686530	single nucleotide variant	NM_139017.7(IL31RA):c.1513A>C (p.Asn505His)	not specified [RCV004929211]	uncertain significance	5	55910543	55910543	Human		name
597774881	CV3686532	single nucleotide variant	NM_139017.7(IL31RA):c.1820A>T (p.Asp607Val)	not specified [RCV004929213]	uncertain significance	5	55916645	55916645	Human		name
597774885	CV3686533	single nucleotide variant	NM_139017.7(IL31RA):c.1886C>A (p.Ser629Tyr)	not specified [RCV004929214]	uncertain significance	5	55916711	55916711	Human		name
597774896	CV3686536	single nucleotide variant	NM_001376923.1(IL32):c.532C>T (p.Pro178Ser)	not specified [RCV004929217]	uncertain significance	16	3069320	3069320	Human		name
597774921	CV3686543	single nucleotide variant	NM_001393494.1(IL34):c.302C>T (p.Ala101Val)	not specified [RCV004929224]	uncertain significance	16	70657021	70657021	Human		name
597774925	CV3686544	single nucleotide variant	NM_001393494.1(IL34):c.677C>G (p.Ser226Cys)	not specified [RCV004929225]	uncertain significance	16	70660135	70660135	Human		name
597774941	CV3686548	single nucleotide variant	NM_001393494.1(IL34):c.656C>A (p.Ser219Tyr)	not specified [RCV004929229]	uncertain significance	16	70660114	70660114	Human		name
597774953	CV3686551	single nucleotide variant	NM_001393494.1(IL34):c.716G>A (p.Gly239Asp)	not specified [RCV004929232]	uncertain significance	16	70660174	70660174	Human		name
598180110	CV3972276	single nucleotide variant	NM_139017.7(IL31RA):c.1727A>T (p.Lys576Ile)	not specified [RCV005352287]	uncertain significance	5	55913561	55913561	Human		name
598180128	CV3972280	single nucleotide variant	NM_139017.7(IL31RA):c.1183G>A (p.Val395Met)	not specified [RCV005352290]	likely benign	5	55906219	55906219	Human		name
598180142	CV3972283	single nucleotide variant	NM_139017.7(IL31RA):c.1778C>T (p.Ala593Val)	not specified [RCV005352292]	uncertain significance	5	55914888	55914888	Human		name
598207602	CV3972284	single nucleotide variant	NM_139017.7(IL31RA):c.1889C>G (p.Thr630Ser)	not specified [RCV005338000]	uncertain significance	5	55916714	55916714	Human		name
598180149	CV3972286	single nucleotide variant	NM_001376923.1(IL32):c.505C>A (p.Pro169Thr)	not specified [RCV005352293]	uncertain significance	16	3069293	3069293	Human		name
598180156	CV3972287	single nucleotide variant	NM_001376923.1(IL32):c.302G>A (p.Gly101Glu)	not specified [RCV005352294]	uncertain significance	16	3069090	3069090	Human		name
598180162	CV3972288	single nucleotide variant	NM_001376923.1(IL32):c.387G>C (p.Trp129Cys)	not specified [RCV005352295]	uncertain significance	16	3069175	3069175	Human		name
598180167	CV3972289	single nucleotide variant	NM_001376923.1(IL32):c.386G>C (p.Trp129Ser)	not specified [RCV005352296]	uncertain significance	16	3069174	3069174	Human		name
598180176	CV3972290	single nucleotide variant	NM_001376923.1(IL32):c.520G>C (p.Glu174Gln)	not specified [RCV005352297]	uncertain significance	16	3069308	3069308	Human		name
598180197	CV3972293	single nucleotide variant	NM_001376923.1(IL32):c.461C>G (p.Ser154Cys)	not specified [RCV005352300]	uncertain significance	16	3069249	3069249	Human		name
598180217	CV3972298	single nucleotide variant	NM_001393494.1(IL34):c.553G>A (p.Val185Ile)	not specified [RCV005352303]	likely benign	16	70660011	70660011	Human		name
598207635	CV3972299	single nucleotide variant	NM_001393494.1(IL34):c.422A>T (p.Lys141Met)	not specified [RCV005338004]	uncertain significance	16	70659637	70659637	Human		name
598207643	CV3972300	single nucleotide variant	NM_001393494.1(IL34):c.629C>T (p.Thr210Ile)	not specified [RCV005338005]	uncertain significance	16	70660087	70660087	Human		name
598180224	CV3972301	single nucleotide variant	NM_001393494.1(IL34):c.655T>C (p.Ser219Pro)	not specified [RCV005352304]	likely benign	16	70660113	70660113	Human		name
598180231	CV3972302	single nucleotide variant	NM_001393494.1(IL34):c.709G>A (p.Gly237Ser)	not specified [RCV005352305]	uncertain significance	16	70660167	70660167	Human		name
598180244	CV3972304	single nucleotide variant	NM_001393494.1(IL34):c.479G>C (p.Arg160Pro)	not specified [RCV005352307]	uncertain significance	16	70659694	70659694	Human		name
8568589	CV39747	single nucleotide variant	NM_139017.7(IL31RA):c.1562C>T (p.Ser521Phe)	Amyloidosis, primary localized cutaneous, 2 [RCV000023775]	pathogenic	5	55910592	55910592	Human	1	name
15184823	CV721483	single nucleotide variant	NM_139017.7(IL31RA):c.1948G>A (p.Glu650Lys)	not provided [RCV000886533]	benign	5	55916773	55916773	Human		name
8631670	CV86874	single nucleotide variant	NM_001242638.1(IL31RA):c.37G>A (p.Gly13Arg)	Malignant melanoma [RCV000066965]	not provided	5	55859539	55859539	Human		name
598227600	CV3892913	deletion	NM_012275.3(IL36RN):c.205_212del (p.Ser69fs)	Acrodermatitis continua suppurativa of Hallopeau [RCV005255239]	pathogenic	2	113062212	113062219	Human	1	name
151829680	CV1480209	deletion	NM_012275.3(IL36RN):c.398_413del (p.Leu133fs)	Generalized pustular psoriasis [RCV001901682]	uncertain significance	2	113062607	113062622	Human	1	name
156311231	CV1913543	deletion	NM_012275.3(IL36RN):c.420_426del (p.Gly141fs)	Generalized pustular psoriasis [RCV002599669]	pathogenic	2	113062626	113062632	Human	1	name

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