| 15190901 | CV777218 | single nucleotide variant | NM_001282857.2(XRN1):c.2617-9T>C | not provided [RCV000954615] | likely benign | 3 | 142380189 | 142380189 | Human | | name |
| 8578080 | CV112458 | single nucleotide variant | NM_001282857.1(XRN1):c.75+5559G>A | Lung cancer [RCV000092981] | uncertain significance | 3 | 142442311 | 142442311 | Human | | name |
| 401771513 | CV2711728 | single nucleotide variant | NM_001282857.2(XRN1):c.4622-385G>C | not specified [RCV004309390] | uncertain significance | 3 | 142313143 | 142313143 | Human | | name |
| 597804800 | CV3630532 | single nucleotide variant | NM_001282857.2(XRN1):c.4622-381G>A | not specified [RCV004882441] | uncertain significance | 3 | 142313139 | 142313139 | Human | | name |
| 407456179 | CV3493705 | single nucleotide variant | NM_001282857.2(XRN1):c.7G>A (p.Val3Ile) | not specified [RCV004685854] | uncertain significance | 3 | 142447938 | 142447938 | Human | | name |
| 401912694 | CV2824987 | single nucleotide variant | NM_001282857.2(XRN1):c.228A>G (p.Lys76=) | not provided [RCV003427436] | likely benign | 3 | 142432741 | 142432741 | Human | | name |
| 407456182 | CV3493706 | single nucleotide variant | NM_001282857.2(XRN1):c.14A>G (p.Lys5Arg) | not specified [RCV004685855] | uncertain significance | 3 | 142447931 | 142447931 | Human | | name |
| 155904641 | CV2349533 | single nucleotide variant | NM_001282857.2(XRN1):c.173A>G (p.Asp58Gly) | not specified [RCV004201920] | uncertain significance | 3 | 142432796 | 142432796 | Human | | name |
| 155933304 | CV2372253 | single nucleotide variant | NM_001282857.2(XRN1):c.151G>A (p.Val51Ile) | not specified [RCV004217031] | uncertain significance | 3 | 142432818 | 142432818 | Human | | name |
| 329357210 | CV2431280 | single nucleotide variant | NM_001282857.2(XRN1):c.170A>T (p.Asp57Val) | not specified [RCV004250613] | uncertain significance | 3 | 142432799 | 142432799 | Human | | name |
| 407456148 | CV3493693 | single nucleotide variant | NM_001282857.2(XRN1):c.235A>G (p.Lys79Glu) | not specified [RCV004685843] | uncertain significance | 3 | 142432734 | 142432734 | Human | | name |
| 597804804 | CV3630534 | single nucleotide variant | NM_001282857.2(XRN1):c.217C>T (p.Arg73Cys) | not specified [RCV004882443] | uncertain significance | 3 | 142432752 | 142432752 | Human | | name |
| 598195653 | CV3933814 | single nucleotide variant | NM_001282857.2(XRN1):c.185C>T (p.Thr62Ile) | not specified [RCV005313368] | uncertain significance | 3 | 142432784 | 142432784 | Human | | name |
| 155915345 | CV2243742 | single nucleotide variant | NM_001282857.2(XRN1):c.938C>T (p.Thr313Ile) | not specified [RCV004114440] | uncertain significance | 3 | 142422611 | 142422611 | Human | | name |
| 156095449 | CV2310105 | single nucleotide variant | NM_001282857.2(XRN1):c.698A>G (p.Lys233Arg) | not specified [RCV004163230] | uncertain significance | 3 | 142423572 | 142423572 | Human | | name |
| 155927760 | CV2391515 | single nucleotide variant | NM_001282857.2(XRN1):c.973A>G (p.Ile325Val) | not specified [RCV004239900] | uncertain significance | 3 | 142421538 | 142421538 | Human | | name |
| 329388275 | CV2437258 | single nucleotide variant | NM_001282857.2(XRN1):c.709C>T (p.Arg237Trp) | not specified [RCV004256145] | uncertain significance | 3 | 142423561 | 142423561 | Human | | name |
| 329394186 | CV2472369 | single nucleotide variant | NM_001282857.2(XRN1):c.782A>C (p.Glu261Ala) | not specified [RCV004285248] | uncertain significance | 3 | 142422851 | 142422851 | Human | | name |
| 401775478 | CV2692388 | single nucleotide variant | NM_001282857.2(XRN1):c.346A>T (p.Ile116Leu) | not specified [RCV004310364] | uncertain significance | 3 | 142426804 | 142426804 | Human | | name |
| 401737305 | CV2718066 | single nucleotide variant | NM_001282857.2(XRN1):c.995A>G (p.Asn332Ser) | not specified [RCV004315788] | uncertain significance | 3 | 142421516 | 142421516 | Human | | name |
| 401881288 | CV2763245 | single nucleotide variant | NM_001282857.2(XRN1):c.715T>C (p.Cys239Arg) | not specified [RCV004336277] | uncertain significance | 3 | 142422918 | 142422918 | Human | | name |
| 407424895 | CV3410846 | single nucleotide variant | NM_001282857.2(XRN1):c.624C>A (p.Asp208Glu) | Neurodevelopmental disorder [RCV004586490] | uncertain significance | 3 | 142425225 | 142425225 | Human | 1 | name |
| 407456157 | CV3493697 | single nucleotide variant | NM_001282857.2(XRN1):c.887A>C (p.His296Pro) | not specified [RCV004685846] | uncertain significance | 3 | 142422662 | 142422662 | Human | | name |
| 407456168 | CV3493701 | single nucleotide variant | NM_001282857.2(XRN1):c.412G>A (p.Glu138Lys) | not specified [RCV004685850] | uncertain significance | 3 | 142425533 | 142425533 | Human | | name |
| 407456177 | CV3493704 | single nucleotide variant | NM_001282857.2(XRN1):c.370A>G (p.Thr124Ala) | not specified [RCV004685853] | uncertain significance | 3 | 142426780 | 142426780 | Human | | name |
| 597804795 | CV3630529 | single nucleotide variant | NM_001282857.2(XRN1):c.692G>A (p.Gly231Asp) | not specified [RCV004882438] | uncertain significance | 3 | 142423578 | 142423578 | Human | | name |
| 598241756 | CV3933812 | single nucleotide variant | NM_001282857.2(XRN1):c.631A>G (p.Met211Val) | not specified [RCV005296987] | uncertain significance | 3 | 142423639 | 142423639 | Human | | name |
| 15199632 | CV720223 | single nucleotide variant | NM_001282857.2(XRN1):c.4230T>C (p.Tyr1410=) | not provided [RCV000890686] | benign | 3 | 142329608 | 142329608 | Human | | name |
| 156243807 | CV2207132 | single nucleotide variant | NM_001282857.2(XRN1):c.1159A>G (p.Lys387Glu) | not specified [RCV004087873] | uncertain significance | 3 | 142421030 | 142421030 | Human | | name |
| 156135689 | CV2213463 | single nucleotide variant | NM_001282857.2(XRN1):c.2139A>C (p.Lys713Asn) | not specified [RCV004087435] | uncertain significance | 3 | 142400512 | 142400512 | Human | | name |
| 155973875 | CV2239044 | single nucleotide variant | NM_001282857.2(XRN1):c.1273C>G (p.Leu425Val) | not specified [RCV004109922] | uncertain significance | 3 | 142418577 | 142418577 | Human | | name |
| 155914296 | CV2242666 | single nucleotide variant | NM_001282857.2(XRN1):c.2569A>T (p.Ser857Cys) | not specified [RCV004113717] | uncertain significance | 3 | 142383347 | 142383347 | Human | | name |
| 156258615 | CV2274046 | single nucleotide variant | NM_001282857.2(XRN1):c.1403A>G (p.His468Arg) | not specified [RCV004134702] | uncertain significance | 3 | 142417173 | 142417173 | Human | | name |
| 156196015 | CV2319018 | single nucleotide variant | NM_001282857.2(XRN1):c.2639T>C (p.Ile880Thr) | not specified [RCV004178107] | uncertain significance | 3 | 142380158 | 142380158 | Human | | name |
| 156292348 | CV2321203 | single nucleotide variant | NM_001282857.2(XRN1):c.2740G>A (p.Gly914Arg) | not specified [RCV004175323] | uncertain significance | 3 | 142376570 | 142376570 | Human | | name |
| 156172227 | CV2326769 | single nucleotide variant | NM_001282857.2(XRN1):c.2518G>A (p.Asp840Asn) | not specified [RCV004176612] | uncertain significance | 3 | 142383398 | 142383398 | Human | | name |
| 156167212 | CV2330180 | single nucleotide variant | NM_001282857.2(XRN1):c.1562C>T (p.Ala521Val) | not specified [RCV004185665] | uncertain significance | 3 | 142414166 | 142414166 | Human | | name |
| 155970982 | CV2334165 | single nucleotide variant | NM_001282857.2(XRN1):c.1903G>C (p.Asp635His) | not specified [RCV004186155] | uncertain significance | 3 | 142403970 | 142403970 | Human | | name |
| 329384548 | CV2435130 | single nucleotide variant | NM_001282857.2(XRN1):c.2066T>C (p.Met689Thr) | not specified [RCV004252771] | uncertain significance | 3 | 142403711 | 142403711 | Human | | name |
| 329368429 | CV2453270 | single nucleotide variant | NM_001282857.2(XRN1):c.1403A>C (p.His468Pro) | not specified [RCV004266909] | uncertain significance | 3 | 142417173 | 142417173 | Human | | name |
| 329393280 | CV2469226 | single nucleotide variant | NM_001282857.2(XRN1):c.2107G>A (p.Val703Ile) | not specified [RCV004280571] | likely benign | 3 | 142400544 | 142400544 | Human | | name |
| 401723600 | CV2675012 | single nucleotide variant | NM_001282857.2(XRN1):c.1319C>T (p.Thr440Met) | not specified [RCV004296315] | uncertain significance | 3 | 142418531 | 142418531 | Human | | name |
| 401766678 | CV2725670 | single nucleotide variant | NM_001282857.2(XRN1):c.2668A>C (p.Ser890Arg) | not specified [RCV004322039] | uncertain significance | 3 | 142380129 | 142380129 | Human | | name |
| 401755429 | CV2732827 | single nucleotide variant | NM_001282857.2(XRN1):c.1112A>G (p.Asn371Ser) | not specified [RCV004332619] | uncertain significance | 3 | 142421077 | 142421077 | Human | | name |
| 401878633 | CV2754723 | single nucleotide variant | NM_001282857.2(XRN1):c.1043G>A (p.Arg348Gln) | not specified [RCV004339391] | uncertain significance | 3 | 142421146 | 142421146 | Human | | name |
| 405667062 | CV3349671 | single nucleotide variant | NM_001282857.2(XRN1):c.1476A>G (p.Ile492Met) | not specified [RCV004485698] | uncertain significance | 3 | 142414252 | 142414252 | Human | | name |
| 405667070 | CV3349673 | single nucleotide variant | NM_001282857.2(XRN1):c.1859C>T (p.Pro620Leu) | not specified [RCV004485700] | uncertain significance | 3 | 142404931 | 142404931 | Human | | name |
| 405667075 | CV3349674 | single nucleotide variant | NM_001282857.2(XRN1):c.2186C>G (p.Ala729Gly) | not specified [RCV004485701] | likely benign | 3 | 142400465 | 142400465 | Human | | name |
| 405667079 | CV3349675 | single nucleotide variant | NM_001282857.2(XRN1):c.2269T>C (p.Ser757Pro) | not specified [RCV004485702] | uncertain significance | 3 | 142397399 | 142397399 | Human | | name |
| 405667084 | CV3349676 | single nucleotide variant | NM_001282857.2(XRN1):c.2272A>G (p.Lys758Glu) | not specified [RCV004485703] | uncertain significance | 3 | 142397396 | 142397396 | Human | | name |
| 405667095 | CV3349678 | single nucleotide variant | NM_001282857.2(XRN1):c.2308T>A (p.Trp770Arg) | not specified [RCV004485705] | uncertain significance | 3 | 142397360 | 142397360 | Human | | name |
| 405667100 | CV3349679 | single nucleotide variant | NM_001282857.2(XRN1):c.2941T>C (p.Ser981Pro) | not specified [RCV004485706] | uncertain significance | 3 | 142375835 | 142375835 | Human | | name |
| 407456152 | CV3493694 | single nucleotide variant | NM_001282857.2(XRN1):c.1502A>G (p.His501Arg) | not specified [RCV004685844] | uncertain significance | 3 | 142414226 | 142414226 | Human | | name |
| 407456153 | CV3493696 | single nucleotide variant | NM_001282857.2(XRN1):c.2011T>A (p.Leu671Met) | not specified [RCV004685845] | uncertain significance | 3 | 142403766 | 142403766 | Human | | name |
| 407456160 | CV3493698 | single nucleotide variant | NM_001282857.2(XRN1):c.2435G>A (p.Gly812Asp) | not specified [RCV004685847] | uncertain significance | 3 | 142384590 | 142384590 | Human | | name |
| 597804797 | CV3630530 | single nucleotide variant | NM_001282857.2(XRN1):c.2432A>G (p.Asn811Ser) | not specified [RCV004882439] | uncertain significance | 3 | 142384593 | 142384593 | Human | | name |
| 597804799 | CV3630531 | single nucleotide variant | NM_001282857.2(XRN1):c.2362A>G (p.Ile788Val) | not specified [RCV004882440] | uncertain significance | 3 | 142384663 | 142384663 | Human | | name |
| 597751782 | CV3630535 | single nucleotide variant | NM_001282857.2(XRN1):c.1350C>G (p.Asp450Glu) | not specified [RCV004892820] | uncertain significance | 3 | 142417226 | 142417226 | Human | | name |
| 597804808 | CV3630539 | single nucleotide variant | NM_001282857.2(XRN1):c.1336G>A (p.Val446Ile) | not specified [RCV004882445] | likely benign | 3 | 142418514 | 142418514 | Human | | name |
| 597751797 | CV3630540 | single nucleotide variant | NM_001282857.2(XRN1):c.2608A>G (p.Thr870Ala) | not specified [RCV004892823] | uncertain significance | 3 | 142383308 | 142383308 | Human | | name |
| 597804810 | CV3630542 | single nucleotide variant | NM_001282857.2(XRN1):c.2374A>T (p.Thr792Ser) | not specified [RCV004882446] | uncertain significance | 3 | 142384651 | 142384651 | Human | | name |
| 597751802 | CV3630543 | single nucleotide variant | NM_001282857.2(XRN1):c.2621A>G (p.Gln874Arg) | not specified [RCV004892824] | uncertain significance | 3 | 142380176 | 142380176 | Human | | name |
| 597804812 | CV3630544 | single nucleotide variant | NM_001282857.2(XRN1):c.1238A>C (p.Lys413Thr) | not specified [RCV004882447] | uncertain significance | 3 | 142418817 | 142418817 | Human | | name |
| 598195642 | CV3933807 | single nucleotide variant | NM_001282857.2(XRN1):c.2290G>C (p.Asp764His) | not specified [RCV005313366] | uncertain significance | 3 | 142397378 | 142397378 | Human | | name |
| 598241740 | CV3933809 | single nucleotide variant | NM_001282857.2(XRN1):c.2605T>C (p.Cys869Arg) | not specified [RCV005296984] | uncertain significance | 3 | 142383311 | 142383311 | Human | | name |
| 598241750 | CV3933811 | single nucleotide variant | NM_001282857.2(XRN1):c.1610A>G (p.Glu537Gly) | not specified [RCV005296986] | uncertain significance | 3 | 142412647 | 142412647 | Human | | name |
| 598195648 | CV3933813 | single nucleotide variant | NM_001282857.2(XRN1):c.2050C>T (p.Arg684Cys) | not specified [RCV005313367] | uncertain significance | 3 | 142403727 | 142403727 | Human | | name |
| 598241762 | CV3933815 | single nucleotide variant | NM_001282857.2(XRN1):c.1363C>G (p.Gln455Glu) | not specified [RCV005296988] | uncertain significance | 3 | 142417213 | 142417213 | Human | | name |
| 151352321 | CV1321231 | single nucleotide variant | NM_001282857.2(XRN1):c.4277T>C (p.Met1426Thr) | not provided [RCV001811724] | uncertain significance | 3 | 142329561 | 142329561 | Human | | name |
| 155926543 | CV2208225 | single nucleotide variant | NM_001282857.2(XRN1):c.4658C>T (p.Ser1553Leu) | not specified [RCV004088681] | uncertain significance | 3 | 142312722 | 142312722 | Human | | name |
| 156279864 | CV2224015 | single nucleotide variant | NM_001282857.2(XRN1):c.4610C>T (p.Pro1537Leu) | not specified [RCV004095891] | uncertain significance | 3 | 142318603 | 142318603 | Human | | name |
| 156112881 | CV2228592 | single nucleotide variant | NM_001282857.2(XRN1):c.4018G>A (p.Glu1340Lys) | not specified [RCV004092822] | uncertain significance | 3 | 142333011 | 142333011 | Human | | name |
| 156020184 | CV2270209 | single nucleotide variant | NM_001282857.2(XRN1):c.3639C>A (p.Asn1213Lys) | not specified [RCV004135432] | uncertain significance | 3 | 142356945 | 142356945 | Human | | name |
| 155923055 | CV2280208 | single nucleotide variant | NM_001282857.2(XRN1):c.4648C>A (p.Leu1550Ile) | not specified [RCV004140429] | uncertain significance | 3 | 142312732 | 142312732 | Human | | name |
| 156177074 | CV2331216 | single nucleotide variant | NM_001282857.2(XRN1):c.4676C>T (p.Ser1559Leu) | not specified [RCV004181819] | uncertain significance | 3 | 142312704 | 142312704 | Human | | name |
| 156053427 | CV2333291 | single nucleotide variant | NM_001282857.2(XRN1):c.3989A>C (p.Glu1330Ala) | not specified [RCV004197039] | uncertain significance | 3 | 142333040 | 142333040 | Human | | name |
| 156198863 | CV2392209 | single nucleotide variant | NM_001282857.2(XRN1):c.4414G>A (p.Val1472Ile) | not specified [RCV004243823] | uncertain significance | 3 | 142318894 | 142318894 | Human | | name |
| 329376925 | CV2435745 | single nucleotide variant | NM_001282857.2(XRN1):c.4949C>T (p.Pro1650Leu) | not specified [RCV004253374] | uncertain significance | 3 | 142311647 | 142311647 | Human | | name |
| 329382564 | CV2449136 | single nucleotide variant | NM_001282857.2(XRN1):c.4801G>A (p.Ala1601Thr) | not specified [RCV004264195] | uncertain significance | 3 | 142311795 | 142311795 | Human | | name |
| 329398376 | CV2464504 | single nucleotide variant | NM_001282857.2(XRN1):c.5068T>G (p.Ser1690Ala) | not specified [RCV004276421] | uncertain significance | 3 | 142311528 | 142311528 | Human | | name |
| 329393481 | CV2467014 | single nucleotide variant | NM_001282857.2(XRN1):c.3593A>G (p.His1198Arg) | not specified [RCV004282759] | uncertain significance | 3 | 142356991 | 142356991 | Human | | name |
| 401743100 | CV2684015 | single nucleotide variant | NM_001282857.2(XRN1):c.3466T>G (p.Cys1156Gly) | not specified [RCV004295620] | uncertain significance | 3 | 142357118 | 142357118 | Human | | name |
| 401772905 | CV2698025 | single nucleotide variant | NM_001282857.2(XRN1):c.4585C>T (p.Pro1529Ser) | not specified [RCV004302828] | uncertain significance | 3 | 142318628 | 142318628 | Human | | name |
| 401762402 | CV2714127 | single nucleotide variant | NM_001282857.2(XRN1):c.3835A>G (p.Ser1279Gly) | not specified [RCV004317381] | uncertain significance | 3 | 142347276 | 142347276 | Human | | name |
| 401724555 | CV2714888 | single nucleotide variant | NM_001282857.2(XRN1):c.3530G>A (p.Arg1177His) | not specified [RCV004322224] | uncertain significance | 3 | 142357054 | 142357054 | Human | | name |
| 401857525 | CV2756013 | single nucleotide variant | NM_001282857.2(XRN1):c.3676C>T (p.Pro1226Ser) | not specified [RCV004338140] | likely benign | 3 | 142355493 | 142355493 | Human | | name |
| 401874699 | CV2759328 | single nucleotide variant | NM_001282857.2(XRN1):c.4057G>A (p.Ala1353Thr) | not specified [RCV004335911] | uncertain significance | 3 | 142332972 | 142332972 | Human | | name |
| 401866122 | CV2762533 | single nucleotide variant | NM_001282857.2(XRN1):c.3359T>C (p.Val1120Ala) | not specified [RCV004338067] | uncertain significance | 3 | 142365082 | 142365082 | Human | | name |
| 401886366 | CV2771196 | single nucleotide variant | NM_001282857.2(XRN1):c.3809A>G (p.His1270Arg) | not specified [RCV004346184] | uncertain significance | 3 | 142347302 | 142347302 | Human | | name |
| 401892049 | CV2775905 | single nucleotide variant | NM_001282857.2(XRN1):c.3927G>T (p.Met1309Ile) | not specified [RCV004344935] | uncertain significance | 3 | 142335460 | 142335460 | Human | | name |
| 405667105 | CV3349680 | single nucleotide variant | NM_001282857.2(XRN1):c.3001A>G (p.Ile1001Val) | not specified [RCV004485707] | uncertain significance | 3 | 142371306 | 142371306 | Human | | name |
| 405667109 | CV3349681 | single nucleotide variant | NM_001282857.2(XRN1):c.3919C>G (p.Gln1307Glu) | not specified [RCV004485708] | uncertain significance | 3 | 142335468 | 142335468 | Human | | name |
| 405667114 | CV3349682 | single nucleotide variant | NM_001282857.2(XRN1):c.4073G>A (p.Arg1358Gln) | not specified [RCV004485709] | uncertain significance | 3 | 142332524 | 142332524 | Human | | name |
| 405667120 | CV3349683 | single nucleotide variant | NM_001282857.2(XRN1):c.4633C>G (p.Pro1545Ala) | not specified [RCV004485710] | uncertain significance | 3 | 142312747 | 142312747 | Human | | name |
| 405667126 | CV3349684 | single nucleotide variant | NM_001282857.2(XRN1):c.4723A>G (p.Thr1575Ala) | not specified [RCV004485711] | uncertain significance | 3 | 142312657 | 142312657 | Human | | name |
| 405667131 | CV3349685 | single nucleotide variant | NM_001282857.2(XRN1):c.4735G>A (p.Ala1579Thr) | not specified [RCV004485712] | uncertain significance | 3 | 142312645 | 142312645 | Human | | name |
| 405667135 | CV3349686 | single nucleotide variant | NM_001282857.2(XRN1):c.4903C>T (p.Arg1635Trp) | not specified [RCV004485713] | uncertain significance | 3 | 142311693 | 142311693 | Human | | name |
| 405667140 | CV3349687 | single nucleotide variant | NM_001282857.2(XRN1):c.4948C>T (p.Pro1650Ser) | not specified [RCV004485714] | uncertain significance | 3 | 142311648 | 142311648 | Human | | name |
| 405667143 | CV3349688 | single nucleotide variant | NM_001282857.2(XRN1):c.4964A>C (p.Gln1655Pro) | not specified [RCV004485715] | uncertain significance | 3 | 142311632 | 142311632 | Human | | name |
| 407456145 | CV3493692 | single nucleotide variant | NM_001282857.2(XRN1):c.3058A>G (p.Asn1020Asp) | not specified [RCV004685842] | uncertain significance | 3 | 142371249 | 142371249 | Human | | name |
| 407465687 | CV3493695 | single nucleotide variant | NM_001282857.2(XRN1):c.3411T>G (p.Asp1137Glu) | not specified [RCV004688837] | uncertain significance | 3 | 142359915 | 142359915 | Human | | name |
| 407456166 | CV3493700 | single nucleotide variant | NM_001282857.2(XRN1):c.4180G>A (p.Glu1394Lys) | not specified [RCV004685849] | uncertain significance | 3 | 142332417 | 142332417 | Human | | name |
| 407456171 | CV3493702 | single nucleotide variant | NM_001282857.2(XRN1):c.3549G>C (p.Gln1183His) | not specified [RCV004685851] | uncertain significance | 3 | 142357035 | 142357035 | Human | | name |
| 407456174 | CV3493703 | single nucleotide variant | NM_001282857.2(XRN1):c.3159T>G (p.Asp1053Glu) | not specified [RCV004685852] | uncertain significance | 3 | 142370530 | 142370530 | Human | | name |
| 597804802 | CV3630533 | single nucleotide variant | NM_001282857.2(XRN1):c.4007C>T (p.Ser1336Phe) | not specified [RCV004882442] | uncertain significance | 3 | 142333022 | 142333022 | Human | | name |
| 597751786 | CV3630536 | single nucleotide variant | NM_001282857.2(XRN1):c.4952C>T (p.Ala1651Val) | not specified [RCV004892821] | uncertain significance | 3 | 142311644 | 142311644 | Human | | name |
| 597751791 | CV3630537 | single nucleotide variant | NM_001282857.2(XRN1):c.3122C>T (p.Thr1041Ile) | not specified [RCV004892822] | uncertain significance | 3 | 142370567 | 142370567 | Human | | name |
| 597804806 | CV3630538 | single nucleotide variant | NM_001282857.2(XRN1):c.4465C>G (p.His1489Asp) | not specified [RCV004882444] | uncertain significance | 3 | 142318843 | 142318843 | Human | | name |
| 597804814 | CV3630545 | single nucleotide variant | NM_001282857.2(XRN1):c.5026T>C (p.Ser1676Pro) | not specified [RCV004882448] | uncertain significance | 3 | 142311570 | 142311570 | Human | | name |
| 598241735 | CV3933808 | single nucleotide variant | NM_001282857.2(XRN1):c.4561G>T (p.Ala1521Ser) | not specified [RCV005296983] | uncertain significance | 3 | 142318652 | 142318652 | Human | | name |
| 598195658 | CV3933816 | single nucleotide variant | NM_001282857.2(XRN1):c.3424G>A (p.Val1142Ile) | not specified [RCV005313369] | uncertain significance | 3 | 142359902 | 142359902 | Human | | name |
