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