| 405272671 | CV3220296 | single nucleotide variant | NM_018012.4(KIF26B):c.2098+9G>A | KIF26B-related disorder [RCV003972224] | benign | 1 | 245611985 | 245611985 | Human | | name , trait , alternate_id |
| 15192358 | CV729993 | single nucleotide variant | NM_018012.4(KIF26B):c.6178+9G>A | KIF26B-related disorder [RCV003940610]|not provided [RCV000888641] | benign | 1 | 245699046 | 245699046 | Human | | name , trait , alternate_id |
| 150533438 | CV1292738 | deletion | NM_018012.4(KIF26B):c.2421+25del | not provided [RCV001754346] | benign | 1 | 245684414 | 245684414 | Human | | name |
| 405289935 | CV3219050 | single nucleotide variant | NM_018012.4(KIF26B):c.1350+10T>C | KIF26B-related disorder [RCV003962039] | likely benign | 1 | 245540960 | 245540960 | Human | | name , trait , alternate_id |
| 8575876 | CV110229 | single nucleotide variant | NM_018012.3(KIF26B):c.999+23042G>A | Lung cancer [RCV000090752] | uncertain significance | 1 | 245390409 | 245390409 | Human | | name |
| 8575880 | CV110233 | single nucleotide variant | NM_018012.3(KIF26B):c.2098+3070C>G | Lung cancer [RCV000090756] | uncertain significance | 1 | 245615046 | 245615046 | Human | | name |
| 8575877 | CV110230 | single nucleotide variant | NM_018012.3(KIF26B):c.1000-12666G>T | Lung cancer [RCV000090753] | uncertain significance | 1 | 245406913 | 245406913 | Human | | name |
| 8575879 | CV110232 | single nucleotide variant | NM_018012.3(KIF26B):c.1167-48523C>T | Lung cancer [RCV000090755] | uncertain significance | 1 | 245492244 | 245492244 | Human | | name |
| 155969479 | CV2337958 | single nucleotide variant | NM_018012.4(KIF26B):c.20A>T (p.Asn7Ile) | not specified [RCV004186005] | uncertain significance | 1 | 245155444 | 245155444 | Human | | name |
| 405265054 | CV3190388 | single nucleotide variant | NM_018012.4(KIF26B):c.222C>G (p.Gly74=) | KIF26B-related disorder [RCV003897238] | likely benign | 1 | 245156440 | 245156440 | Human | | name , trait , alternate_id |
| 405276482 | CV3198511 | single nucleotide variant | NM_018012.4(KIF26B):c.171G>A (p.Glu57=) | KIF26B-related disorder [RCV003903843] | benign | 1 | 245156389 | 245156389 | Human | | name , trait , alternate_id |
| 408367007 | CV3510061 | single nucleotide variant | NM_018012.4(KIF26B):c.195C>A (p.Ser65=) | KIF26B-related disorder [RCV004757698] | likely benign | 1 | 245156413 | 245156413 | Human | | name , trait , alternate_id |
| 329358537 | CV2425220 | single nucleotide variant | NM_018012.4(KIF26B):c.82C>T (p.Pro28Ser) | not specified [RCV004250892] | uncertain significance | 1 | 245156300 | 245156300 | Human | | name |
| 401937167 | CV2812919 | single nucleotide variant | NM_018012.4(KIF26B):c.507C>T (p.Val169=) | KIF26B-related disorder [RCV003980867]|not provided [RCV003415099] | benign|likely benign | 1 | 245366875 | 245366875 | Human | | name , trait , alternate_id |
| 405281065 | CV3190742 | single nucleotide variant | NM_018012.4(KIF26B):c.534C>T (p.Asn178=) | KIF26B-related disorder [RCV003907177] | likely benign | 1 | 245366902 | 245366902 | Human | | name , trait , alternate_id |
| 405281471 | CV3191718 | single nucleotide variant | NM_018012.4(KIF26B):c.651G>A (p.Ser217=) | KIF26B-related disorder [RCV003907330] | likely benign | 1 | 245367019 | 245367019 | Human | | name , trait , alternate_id |
| 405285074 | CV3202374 | single nucleotide variant | NM_018012.4(KIF26B):c.453C>T (p.Pro151=) | KIF26B-related disorder [RCV003909644] | likely benign | 1 | 245156671 | 245156671 | Human | | name , trait , alternate_id |
| 405261694 | CV3205280 | single nucleotide variant | NM_018012.4(KIF26B):c.876C>T (p.Leu292=) | KIF26B-related disorder [RCV003944612] | likely benign | 1 | 245367244 | 245367244 | Human | | name , trait , alternate_id |
| 405282371 | CV3212801 | single nucleotide variant | NM_018012.4(KIF26B):c.582G>A (p.Leu194=) | KIF26B-related disorder [RCV003956949] | likely benign | 1 | 245366950 | 245366950 | Human | | name , trait , alternate_id |
| 405272539 | CV3220294 | single nucleotide variant | NM_018012.4(KIF26B):c.447G>C (p.Pro149=) | KIF26B-related disorder [RCV003972223] | likely benign | 1 | 245156665 | 245156665 | Human | | name , trait , alternate_id |
| 15168422 | CV718843 | single nucleotide variant | NM_018012.4(KIF26B):c.975C>T (p.Asn325=) | KIF26B-related disorder [RCV003920582]|not provided [RCV000883060] | benign | 1 | 245367343 | 245367343 | Human | | name , trait , alternate_id |
| 15163772 | CV732330 | single nucleotide variant | NM_018012.4(KIF26B):c.819C>T (p.Val273=) | not provided [RCV000903849] | likely benign | 1 | 245367187 | 245367187 | Human | | name |
| 151352763 | CV1326001 | single nucleotide variant | NM_018012.4(KIF26B):c.2496C>A (p.Pro832=) | KIF26B-related disorder [RCV003941141]|not provided [RCV001815697] | likely benign | 1 | 245685479 | 245685479 | Human | | name , trait , alternate_id |
| 156340133 | CV2363187 | single nucleotide variant | NM_018012.4(KIF26B):c.271G>A (p.Gly91Ser) | not specified [RCV004213755] | uncertain significance | 1 | 245156489 | 245156489 | Human | | name |
| 401742337 | CV2673758 | single nucleotide variant | NM_018012.4(KIF26B):c.175G>T (p.Ala59Ser) | not specified [RCV004293145] | uncertain significance | 1 | 245156393 | 245156393 | Human | | name |
| 401937164 | CV2812922 | single nucleotide variant | NM_018012.4(KIF26B):c.2286G>A (p.Arg762=) | not provided [RCV003415102] | likely benign | 1 | 245684260 | 245684260 | Human | | name |
| 405281666 | CV3191577 | single nucleotide variant | NM_018012.4(KIF26B):c.2346C>T (p.Val782=) | KIF26B-related disorder [RCV003907313] | benign | 1 | 245684320 | 245684320 | Human | | name , trait , alternate_id |
| 405275611 | CV3196415 | single nucleotide variant | NM_018012.4(KIF26B):c.2136C>T (p.Leu712=) | KIF26B-related disorder [RCV003974252] | likely benign | 1 | 245646158 | 245646158 | Human | | name , trait , alternate_id |
| 405290970 | CV3197180 | single nucleotide variant | NM_018012.4(KIF26B):c.2715C>T (p.Pro905=) | KIF26B-related disorder [RCV003984743] | benign | 1 | 245685698 | 245685698 | Human | | name , trait , alternate_id |
| 405276960 | CV3198678 | single nucleotide variant | NM_018012.4(KIF26B):c.1128T>C (p.Thr376=) | KIF26B-related disorder [RCV003904004] | benign | 1 | 245419707 | 245419707 | Human | | name , trait , alternate_id |
| 405277071 | CV3198714 | single nucleotide variant | NM_018012.4(KIF26B):c.2340C>T (p.Ala780=) | KIF26B-related disorder [RCV003904039] | likely benign | 1 | 245684314 | 245684314 | Human | | name , trait , alternate_id |
| 405280405 | CV3200731 | single nucleotide variant | NM_018012.4(KIF26B):c.1776A>C (p.Ser592=) | KIF26B-related disorder [RCV003977356] | benign | 1 | 245609390 | 245609390 | Human | | name , trait , alternate_id |
| 405289048 | CV3204882 | single nucleotide variant | NM_018012.4(KIF26B):c.2757C>T (p.Asp919=) | KIF26B-related disorder [RCV003961534] | likely benign | 1 | 245685740 | 245685740 | Human | | name , trait , alternate_id |
| 405291655 | CV3205907 | single nucleotide variant | NM_018012.4(KIF26B):c.1848G>A (p.Thr616=) | KIF26B-related disorder [RCV003964021] | likely benign | 1 | 245609462 | 245609462 | Human | | name , trait , alternate_id |
| 405292915 | CV3207025 | single nucleotide variant | NM_018012.4(KIF26B):c.1671C>T (p.Ile557=) | KIF26B-related disorder [RCV003931442] | likely benign | 1 | 245609285 | 245609285 | Human | | name , trait , alternate_id |
| 405273367 | CV3207351 | single nucleotide variant | NM_018012.4(KIF26B):c.1074G>A (p.Lys358=) | KIF26B-related disorder [RCV003914659] | likely benign | 1 | 245419653 | 245419653 | Human | | name , trait , alternate_id |
| 405256030 | CV3208531 | single nucleotide variant | NM_018012.4(KIF26B):c.1227C>T (p.Ser409=) | KIF26B-related disorder [RCV003939613] | likely benign | 1 | 245540827 | 245540827 | Human | | name , trait , alternate_id |
| 405652411 | CV3268878 | single nucleotide variant | NM_018012.4(KIF26B):c.2337G>A (p.Ser779=) | not specified [RCV004414132] | likely benign | 1 | 245684311 | 245684311 | Human | | name |
| 407524933 | CV3452132 | single nucleotide variant | NM_018012.4(KIF26B):c.236G>A (p.Ser79Asn) | not specified [RCV004631450] | uncertain significance | 1 | 245156454 | 245156454 | Human | | name |
| 597630313 | CV3695147 | single nucleotide variant | NM_018012.4(KIF26B):c.1452C>T (p.Tyr484=) | not specified [RCV004939473] | likely benign | 1 | 245602678 | 245602678 | Human | | name |
| 597630223 | CV3698184 | single nucleotide variant | NM_018012.4(KIF26B):c.259C>T (p.Pro87Ser) | not specified [RCV004939457] | uncertain significance | 1 | 245156477 | 245156477 | Human | | name |
| 597630228 | CV3698185 | single nucleotide variant | NM_018012.4(KIF26B):c.156C>G (p.Ser52Arg) | not specified [RCV004939458] | uncertain significance | 1 | 245156374 | 245156374 | Human | | name |
| 598220454 | CV3990975 | single nucleotide variant | NM_018012.4(KIF26B):c.206C>G (p.Pro69Arg) | not specified [RCV005360669] | uncertain significance | 1 | 245156424 | 245156424 | Human | | name |
| 15183552 | CV707261 | single nucleotide variant | NM_018012.4(KIF26B):c.2085C>T (p.Ser695=) | KIF26B-related disorder [RCV003918578]|not provided [RCV000974902] | benign | 1 | 245611963 | 245611963 | Human | | name , trait , alternate_id |
| 15191683 | CV718845 | single nucleotide variant | NM_018012.4(KIF26B):c.2655C>A (p.Gly885=) | KIF26B-related disorder [RCV003910523]|not provided [RCV000888448] | benign | 1 | 245685638 | 245685638 | Human | | name , trait , alternate_id |
| 15145532 | CV732331 | single nucleotide variant | NM_018012.4(KIF26B):c.1791C>A (p.Ala597=) | not provided [RCV000900176] | benign | 1 | 245609405 | 245609405 | Human | | name |
| 15149381 | CV732332 | single nucleotide variant | NM_018012.4(KIF26B):c.2439C>T (p.Ser813=) | not provided [RCV000900922] | likely benign | 1 | 245685422 | 245685422 | Human | | name |
| 15137962 | CV761833 | single nucleotide variant | NM_018012.4(KIF26B):c.2535C>T (p.Ile845=) | KIF26B-related disorder [RCV003925845]|not provided [RCV000943322] | likely benign | 1 | 245685518 | 245685518 | Human | | name , trait , alternate_id |
| 150447699 | CV1253441 | single nucleotide variant | NM_018012.4(KIF26B):c.5988C>T (p.Asp1996=) | KIF26B-related disorder [RCV003968451]|not provided [RCV001667369] | benign | 1 | 245698269 | 245698269 | Human | | name , trait , alternate_id |
| 156339379 | CV2225082 | single nucleotide variant | NM_018012.4(KIF26B):c.611C>T (p.Thr204Met) | not specified [RCV004094900] | uncertain significance | 1 | 245366979 | 245366979 | Human | | name |
| 156095824 | CV2253069 | single nucleotide variant | NM_018012.4(KIF26B):c.479C>T (p.Ser160Leu) | not specified [RCV004120857] | uncertain significance | 1 | 245366847 | 245366847 | Human | | name |
| 155992802 | CV2281248 | single nucleotide variant | NM_018012.4(KIF26B):c.974A>G (p.Asn325Ser) | not specified [RCV004147495] | uncertain significance | 1 | 245367342 | 245367342 | Human | | name |
| 156072864 | CV2295996 | single nucleotide variant | NM_018012.4(KIF26B):c.646G>A (p.Ala216Thr) | not specified [RCV004151882] | uncertain significance | 1 | 245367014 | 245367014 | Human | | name |
| 156293739 | CV2336549 | single nucleotide variant | NM_018012.4(KIF26B):c.435G>T (p.Arg145Ser) | not specified [RCV004194754] | uncertain significance | 1 | 245156653 | 245156653 | Human | | name |
| 156144548 | CV2383937 | single nucleotide variant | NM_018012.4(KIF26B):c.673T>G (p.Ser225Ala) | not specified [RCV004231789] | uncertain significance | 1 | 245367041 | 245367041 | Human | | name |
| 401740908 | CV2680505 | single nucleotide variant | NM_018012.4(KIF26B):c.431T>C (p.Leu144Pro) | not specified [RCV004291145] | uncertain significance | 1 | 245156649 | 245156649 | Human | | name |
| 401749019 | CV2713554 | single nucleotide variant | NM_018012.4(KIF26B):c.364G>C (p.Gly122Arg) | not specified [RCV004320936] | uncertain significance | 1 | 245156582 | 245156582 | Human | | name |
| 401937166 | CV2812920 | single nucleotide variant | NM_018012.4(KIF26B):c.913A>C (p.Asn305His) | KIF26B-related disorder [RCV003966348]|not provided [RCV003415100] | likely benign | 1 | 245367281 | 245367281 | Human | | name , trait , alternate_id |
| 401937162 | CV2812924 | single nucleotide variant | NM_018012.4(KIF26B):c.4125G>A (p.Thr1375=) | not provided [RCV003415104] | likely benign | 1 | 245687108 | 245687108 | Human | | name |
| 401937161 | CV2812925 | single nucleotide variant | NM_018012.4(KIF26B):c.5196C>T (p.Ile1732=) | not provided [RCV003415105] | likely benign | 1 | 245688179 | 245688179 | Human | | name |
| 405280843 | CV3190572 | single nucleotide variant | NM_018012.4(KIF26B):c.3975C>T (p.Thr1325=) | KIF26B-related disorder [RCV003907010] | likely benign | 1 | 245686958 | 245686958 | Human | | name , trait , alternate_id |
| 405280354 | CV3191723 | single nucleotide variant | NM_018012.4(KIF26B):c.3684C>T (p.Pro1228=) | KIF26B-related disorder [RCV003919858] | benign | 1 | 245686667 | 245686667 | Human | | name , trait , alternate_id |
| 405286664 | CV3192225 | single nucleotide variant | NM_018012.4(KIF26B):c.3780G>A (p.Pro1260=) | KIF26B-related disorder [RCV003924128] | likely benign | 1 | 245686763 | 245686763 | Human | | name , trait , alternate_id |
| 405275579 | CV3196353 | single nucleotide variant | NM_018012.4(KIF26B):c.5505C>T (p.Ala1835=) | KIF26B-related disorder [RCV003974201] | likely benign | 1 | 245688488 | 245688488 | Human | | name , trait , alternate_id |
| 405262915 | CV3196804 | single nucleotide variant | NM_018012.4(KIF26B):c.5019A>G (p.Thr1673=) | KIF26B-related disorder [RCV003967381] | benign | 1 | 245688002 | 245688002 | Human | | name , trait , alternate_id |
| 405267563 | CV3198377 | single nucleotide variant | NM_018012.4(KIF26B):c.3882G>A (p.Ser1294=) | KIF26B-related disorder [RCV003911747] | likely benign | 1 | 245686865 | 245686865 | Human | | name , trait , alternate_id |
| 405258327 | CV3203660 | single nucleotide variant | NM_018012.4(KIF26B):c.3342G>A (p.Ala1114=) | KIF26B-related disorder [RCV003941855] | benign | 1 | 245686325 | 245686325 | Human | | name , trait , alternate_id |
| 405255980 | CV3208463 | single nucleotide variant | NM_018012.4(KIF26B):c.5055C>T (p.Ala1685=) | KIF26B-related disorder [RCV003939556] | likely benign | 1 | 245688038 | 245688038 | Human | | name , trait , alternate_id |
| 405274760 | CV3209587 | single nucleotide variant | NM_018012.4(KIF26B):c.776G>T (p.Gly259Val) | KIF26B-related disorder [RCV003951847] | benign | 1 | 245367144 | 245367144 | Human | | name , trait , alternate_id |
| 405273105 | CV3210310 | single nucleotide variant | NM_018012.4(KIF26B):c.5982C>T (p.Ile1994=) | KIF26B-related disorder [RCV003914538] | benign | 1 | 245698263 | 245698263 | Human | | name , trait , alternate_id |
| 405261849 | CV3216389 | single nucleotide variant | NM_018012.4(KIF26B):c.3033G>A (p.Ala1011=) | KIF26B-related disorder [RCV003944620] | likely benign | 1 | 245686016 | 245686016 | Human | | name , trait , alternate_id |
| 405277171 | CV3217705 | single nucleotide variant | NM_018012.4(KIF26B):c.3810C>T (p.Asp1270=) | KIF26B-related disorder [RCV003974770] | benign | 1 | 245686793 | 245686793 | Human | | name , trait , alternate_id |
| 405287777 | CV3217907 | single nucleotide variant | NM_018012.4(KIF26B):c.3057G>A (p.Pro1019=) | KIF26B-related disorder [RCV003982030] | benign | 1 | 245686040 | 245686040 | Human | | name , trait , alternate_id |
| 405271054 | CV3218868 | single nucleotide variant | NM_018012.4(KIF26B):c.5211A>G (p.Arg1737=) | KIF26B-related disorder [RCV003971616] | benign | 1 | 245688194 | 245688194 | Human | | name , trait , alternate_id |
| 405291974 | CV3221191 | single nucleotide variant | NM_018012.4(KIF26B):c.3132G>A (p.Gln1044=) | KIF26B-related disorder [RCV003964281] | likely benign | 1 | 245686115 | 245686115 | Human | | name , trait , alternate_id |
| 405278081 | CV3221670 | single nucleotide variant | NM_018012.4(KIF26B):c.4521G>A (p.Arg1507=) | KIF26B-related disorder [RCV003976279] | benign | 1 | 245687504 | 245687504 | Human | | name , trait , alternate_id |
| 405652489 | CV3268893 | single nucleotide variant | NM_018012.4(KIF26B):c.458C>T (p.Pro153Leu) | not specified [RCV004414147] | uncertain significance | 1 | 245156676 | 245156676 | Human | | name |
| 405652524 | CV3268910 | single nucleotide variant | NM_018012.4(KIF26B):c.620A>C (p.Gln207Pro) | not specified [RCV004414164] | uncertain significance | 1 | 245366988 | 245366988 | Human | | name |
| 405652526 | CV3268911 | single nucleotide variant | NM_018012.4(KIF26B):c.650C>T (p.Ser217Leu) | not specified [RCV004414165] | uncertain significance | 1 | 245367018 | 245367018 | Human | | name |
| 407524878 | CV3452133 | single nucleotide variant | NM_018012.4(KIF26B):c.422G>A (p.Arg141Lys) | not specified [RCV004631451] | uncertain significance | 1 | 245156640 | 245156640 | Human | | name |
| 407524651 | CV3452137 | single nucleotide variant | NM_018012.4(KIF26B):c.826G>A (p.Gly276Arg) | not specified [RCV004631454] | uncertain significance | 1 | 245367194 | 245367194 | Human | | name |
| 407524663 | CV3452143 | single nucleotide variant | NM_018012.4(KIF26B):c.3567G>A (p.Val1189=) | not specified [RCV004631460] | likely benign | 1 | 245686550 | 245686550 | Human | | name |
| 407524685 | CV3452149 | single nucleotide variant | NM_018012.4(KIF26B):c.404G>T (p.Arg135Leu) | not specified [RCV004631466] | uncertain significance | 1 | 245156622 | 245156622 | Human | | name |
| 407524688 | CV3452150 | single nucleotide variant | NM_018012.4(KIF26B):c.452C>G (p.Pro151Arg) | not specified [RCV004631467] | uncertain significance | 1 | 245156670 | 245156670 | Human | | name |
| 597630275 | CV3695139 | single nucleotide variant | NM_018012.4(KIF26B):c.715C>T (p.Leu239Phe) | not specified [RCV004939466] | uncertain significance | 1 | 245367083 | 245367083 | Human | | name |
| 597630291 | CV3695142 | single nucleotide variant | NM_018012.4(KIF26B):c.934C>T (p.His312Tyr) | not specified [RCV004939469] | uncertain significance | 1 | 245367302 | 245367302 | Human | | name |
| 597630329 | CV3695150 | single nucleotide variant | NM_018012.4(KIF26B):c.5379G>A (p.Ser1793=) | not specified [RCV004939476] | likely benign | 1 | 245688362 | 245688362 | Human | | name |
| 597630335 | CV3695151 | single nucleotide variant | NM_018012.4(KIF26B):c.373C>A (p.Arg125Ser) | not specified [RCV004939477] | uncertain significance | 1 | 245156591 | 245156591 | Human | | name |
| 597630341 | CV3695153 | single nucleotide variant | NM_018012.4(KIF26B):c.604G>A (p.Val202Met) | not specified [RCV004939478] | uncertain significance | 1 | 245366972 | 245366972 | Human | | name |
| 597630353 | CV3695155 | single nucleotide variant | NM_018012.4(KIF26B):c.761C>A (p.Thr254Asn) | not specified [RCV004939480] | uncertain significance | 1 | 245367129 | 245367129 | Human | | name |
| 597630359 | CV3695156 | single nucleotide variant | NM_018012.4(KIF26B):c.662C>T (p.Pro221Leu) | not specified [RCV004939481] | uncertain significance | 1 | 245367030 | 245367030 | Human | | name |
| 597630381 | CV3695160 | single nucleotide variant | NM_018012.4(KIF26B):c.527C>G (p.Ala176Gly) | not specified [RCV004939485] | uncertain significance | 1 | 245366895 | 245366895 | Human | | name |
| 597630188 | CV3698177 | single nucleotide variant | NM_018012.4(KIF26B):c.340G>A (p.Gly114Ser) | not specified [RCV004939451] | uncertain significance | 1 | 245156558 | 245156558 | Human | | name |
| 597768126 | CV3698178 | single nucleotide variant | NM_018012.4(KIF26B):c.460G>A (p.Gly154Ser) | not specified [RCV004927440] | uncertain significance | 1 | 245156678 | 245156678 | Human | | name |
| 597630195 | CV3698179 | single nucleotide variant | NM_018012.4(KIF26B):c.760A>G (p.Thr254Ala) | not specified [RCV004939452] | uncertain significance | 1 | 245367128 | 245367128 | Human | | name |
| 598127686 | CV3888286 | single nucleotide variant | NM_018012.4(KIF26B):c.698C>A (p.Ser233Tyr) | not provided [RCV005242972] | uncertain significance | 1 | 245367066 | 245367066 | Human | | name |
| 12896398 | CV389389 | single nucleotide variant | NM_018012.4(KIF26B):c.3444G>A (p.Pro1148=) | KIF26B-related disorder [RCV003983070]|not provided [RCV004715212]|not specified [RCV000455291] | benign | 1 | 245686427 | 245686427 | Human | | name , trait , alternate_id |
| 12896068 | CV389392 | single nucleotide variant | NM_018012.4(KIF26B):c.5004G>T (p.Ser1668=) | KIF26B-related disorder [RCV003972716]|not provided [RCV004715214]|not specified [RCV000454839] | benign | 1 | 245687987 | 245687987 | Human | | name , trait , alternate_id |
| 12896981 | CV389430 | single nucleotide variant | NM_018012.4(KIF26B):c.4221G>C (p.Pro1407=) | KIF26B-related disorder [RCV003972715]|not provided [RCV004715213]|not specified [RCV000456079] | benign | 1 | 245687204 | 245687204 | Human | | name , trait , alternate_id |
| 598272495 | CV3990976 | single nucleotide variant | NM_018012.4(KIF26B):c.661C>T (p.Pro221Ser) | not specified [RCV005350504] | uncertain significance | 1 | 245367029 | 245367029 | Human | | name |
| 598272499 | CV3990979 | single nucleotide variant | NM_018012.4(KIF26B):c.520C>T (p.Arg174Trp) | not specified [RCV005350505] | uncertain significance | 1 | 245366888 | 245366888 | Human | | name |
| 598248412 | CV3990983 | single nucleotide variant | NM_018012.4(KIF26B):c.340G>T (p.Gly114Cys) | not specified [RCV005366229] | uncertain significance | 1 | 245156558 | 245156558 | Human | | name |
| 598272507 | CV3990987 | single nucleotide variant | NM_018012.4(KIF26B):c.871A>G (p.Ser291Gly) | not specified [RCV005350507] | uncertain significance | 1 | 245367239 | 245367239 | Human | | name |
| 598220474 | CV3990988 | single nucleotide variant | NM_018012.4(KIF26B):c.700C>T (p.Arg234Trp) | not specified [RCV005360672] | uncertain significance | 1 | 245367068 | 245367068 | Human | | name |
| 616939676 | CV4014173 | single nucleotide variant | NM_018012.4(KIF26B):c.341G>A (p.Gly114Asp) | not provided [RCV005413665] | uncertain significance | 1 | 245156559 | 245156559 | Human | | name |
| 15201110 | CV696636 | single nucleotide variant | NM_018012.4(KIF26B):c.5163C>T (p.Ser1721=) | KIF26B-related disorder [RCV003915940]|not provided [RCV000957527] | benign | 1 | 245688146 | 245688146 | Human | | name , trait , alternate_id |
| 15189094 | CV696638 | single nucleotide variant | NM_018012.4(KIF26B):c.6229C>T (p.Leu2077=) | not provided [RCV000954075] | benign | 1 | 245702508 | 245702508 | Human | | name |
| 15161326 | CV707263 | single nucleotide variant | NM_018012.4(KIF26B):c.3159C>T (p.Cys1053=) | KIF26B-related disorder [RCV003928476]|not provided [RCV000970068] | benign|likely benign | 1 | 245686142 | 245686142 | Human | | name , trait , alternate_id |
| 15164829 | CV707264 | single nucleotide variant | NM_018012.4(KIF26B):c.3231G>A (p.Ser1077=) | KIF26B-related disorder [RCV003918443]|not provided [RCV000970815] | benign | 1 | 245686214 | 245686214 | Human | | name , trait , alternate_id |
| 15173259 | CV707267 | single nucleotide variant | NM_018012.4(KIF26B):c.5304C>A (p.Gly1768=) | KIF26B-related disorder [RCV003962896]|not provided [RCV000972579] | benign|likely benign | 1 | 245688287 | 245688287 | Human | | name , trait , alternate_id |
| 15180162 | CV718848 | single nucleotide variant | NM_018012.4(KIF26B):c.4011C>T (p.Pro1337=) | KIF26B-related disorder [RCV003940523]|not provided [RCV000885461] | benign|likely benign | 1 | 245686994 | 245686994 | Human | | name , trait , alternate_id |
| 15194938 | CV718849 | single nucleotide variant | NM_018012.4(KIF26B):c.4401G>A (p.Thr1467=) | KIF26B-related disorder [RCV003930749]|not provided [RCV000889359] | benign | 1 | 245687384 | 245687384 | Human | | name , trait , alternate_id |
| 15194943 | CV718850 | single nucleotide variant | NM_018012.4(KIF26B):c.4671C>T (p.Cys1557=) | KIF26B-related disorder [RCV003940634]|not provided [RCV000889360] | benign | 1 | 245687654 | 245687654 | Human | | name , trait , alternate_id |
| 15151243 | CV732333 | single nucleotide variant | NM_018012.4(KIF26B):c.3852G>A (p.Glu1284=) | not provided [RCV000901323] | likely benign | 1 | 245686835 | 245686835 | Human | | name |
| 15147286 | CV746374 | single nucleotide variant | NM_018012.4(KIF26B):c.3369G>A (p.Glu1123=) | KIF26B-related disorder [RCV003923294]|not provided [RCV000922878] | likely benign | 1 | 245686352 | 245686352 | Human | | name , trait , alternate_id |
| 151757681 | CV1288082 | single nucleotide variant | NM_018012.4(KIF26B):c.2605G>A (p.Gly869Arg) | Autosomal dominant cerebellar ataxia [RCV001849205] | uncertain significance | 1 | 245685588 | 245685588 | Human | 1 | name |
| 151757834 | CV1288109 | single nucleotide variant | NM_018012.4(KIF26B):c.1340G>A (p.Gly447Glu) | Autosomal dominant cerebellar ataxia [RCV001849232] | uncertain significance | 1 | 245540940 | 245540940 | Human | 1 | name |
| 151757841 | CV1288110 | single nucleotide variant | NM_018012.4(KIF26B):c.2023G>C (p.Asp675His) | Autosomal dominant cerebellar ataxia [RCV001849233] | uncertain significance | 1 | 245611901 | 245611901 | Human | 1 | name |
| 156397857 | CV2193835 | single nucleotide variant | NM_018012.4(KIF26B):c.2699G>A (p.Arg900Gln) | not specified [RCV004074583] | uncertain significance | 1 | 245685682 | 245685682 | Human | | name |
| 156243751 | CV2207119 | single nucleotide variant | NM_018012.4(KIF26B):c.2869G>C (p.Glu957Gln) | not specified [RCV004086069] | uncertain significance | 1 | 245685852 | 245685852 | Human | | name |
| 155987590 | CV2234118 | single nucleotide variant | NM_018012.4(KIF26B):c.1559C>T (p.Ala520Val) | not specified [RCV004106215] | uncertain significance | 1 | 245607652 | 245607652 | Human | | name |
| 156297524 | CV2246861 | single nucleotide variant | NM_018012.4(KIF26B):c.1501C>G (p.Gln501Glu) | not specified [RCV004112672] | uncertain significance | 1 | 245602727 | 245602727 | Human | | name |
| 156261133 | CV2282375 | single nucleotide variant | NM_018012.4(KIF26B):c.2863G>A (p.Gly955Arg) | not specified [RCV004133195] | uncertain significance | 1 | 245685846 | 245685846 | Human | | name |
| 156136563 | CV2284826 | single nucleotide variant | NM_018012.4(KIF26B):c.1141T>C (p.Ser381Pro) | not specified [RCV004143001] | uncertain significance | 1 | 245419720 | 245419720 | Human | | name |
| 156044726 | CV2318958 | single nucleotide variant | NM_018012.4(KIF26B):c.2331C>A (p.His777Gln) | not specified [RCV004176157] | uncertain significance | 1 | 245684305 | 245684305 | Human | | name |
| 156273525 | CV2320192 | single nucleotide variant | NM_018012.4(KIF26B):c.2728G>C (p.Glu910Gln) | not specified [RCV004169815] | uncertain significance | 1 | 245685711 | 245685711 | Human | | name |
| 156057463 | CV2322850 | single nucleotide variant | NM_018012.4(KIF26B):c.2962C>G (p.Leu988Val) | not specified [RCV004185310] | uncertain significance | 1 | 245685945 | 245685945 | Human | | name |
| 156072949 | CV2325383 | single nucleotide variant | NM_018012.4(KIF26B):c.1874C>T (p.Pro625Leu) | not specified [RCV004177752] | uncertain significance | 1 | 245609488 | 245609488 | Human | | name |
| 156255055 | CV2325710 | single nucleotide variant | NM_018012.4(KIF26B):c.1123G>A (p.Glu375Lys) | not specified [RCV004180112] | uncertain significance | 1 | 245419702 | 245419702 | Human | | name |
| 155978839 | CV2339980 | single nucleotide variant | NM_018012.4(KIF26B):c.1453G>A (p.Asp485Asn) | not specified [RCV004192236] | uncertain significance | 1 | 245602679 | 245602679 | Human | | name |
| 156018674 | CV2370312 | single nucleotide variant | NM_018012.4(KIF26B):c.2356G>A (p.Ala786Thr) | not specified [RCV004213225] | uncertain significance | 1 | 245684330 | 245684330 | Human | | name |
| 155995573 | CV2375834 | single nucleotide variant | NM_018012.4(KIF26B):c.1024A>G (p.Ser342Gly) | not specified [RCV004224413] | likely benign | 1 | 245419603 | 245419603 | Human | | name |
| 156043319 | CV2381537 | single nucleotide variant | NM_018012.4(KIF26B):c.1315G>A (p.Val439Ile) | not specified [RCV004230012] | uncertain significance | 1 | 245540915 | 245540915 | Human | | name |
| 155958925 | CV2390441 | single nucleotide variant | NM_018012.4(KIF26B):c.2536G>A (p.Ala846Thr) | not specified [RCV004238984] | uncertain significance | 1 | 245685519 | 245685519 | Human | | name |
| 155934077 | CV2399444 | single nucleotide variant | NM_018012.4(KIF26B):c.1172C>T (p.Ala391Val) | not specified [RCV004242717] | uncertain significance | 1 | 245540772 | 245540772 | Human | | name |
| 329376265 | CV2431787 | single nucleotide variant | NM_018012.4(KIF26B):c.2236G>A (p.Gly746Ser) | not specified [RCV004248946] | uncertain significance | 1 | 245646258 | 245646258 | Human | | name |
| 329401121 | CV2446154 | single nucleotide variant | NM_018012.4(KIF26B):c.2123A>G (p.His708Arg) | not specified [RCV004264565] | uncertain significance | 1 | 245646145 | 245646145 | Human | | name |
| 329396174 | CV2459372 | single nucleotide variant | NM_018012.4(KIF26B):c.2059A>G (p.Ile687Val) | not specified [RCV004275071] | uncertain significance | 1 | 245611937 | 245611937 | Human | | name |
| 401757452 | CV2675312 | single nucleotide variant | NM_018012.4(KIF26B):c.1983T>G (p.Ile661Met) | not specified [RCV004292122] | uncertain significance | 1 | 245611861 | 245611861 | Human | | name |
| 401782510 | CV2686897 | single nucleotide variant | NM_018012.4(KIF26B):c.1090G>A (p.Val364Ile) | not specified [RCV004302071] | uncertain significance | 1 | 245419669 | 245419669 | Human | | name |
| 401749860 | CV2704746 | single nucleotide variant | NM_018012.4(KIF26B):c.2341G>A (p.Ala781Thr) | not specified [RCV004307345] | uncertain significance | 1 | 245684315 | 245684315 | Human | | name |
| 401876100 | CV2789294 | single nucleotide variant | NM_018012.4(KIF26B):c.2662G>A (p.Asp888Asn) | not specified [RCV004365320] | uncertain significance | 1 | 245685645 | 245685645 | Human | | name |
| 401937165 | CV2812921 | single nucleotide variant | NM_018012.4(KIF26B):c.1228G>A (p.Ala410Thr) | KIF26B-related disorder [RCV003966349]|not provided [RCV003415101] | likely benign | 1 | 245540828 | 245540828 | Human | | name , trait , alternate_id |
| 405259610 | CV3195122 | single nucleotide variant | NM_018012.4(KIF26B):c.1264G>A (p.Gly422Arg) | KIF26B-related disorder [RCV003894319] | uncertain significance | 1 | 245540864 | 245540864 | Human | | name , trait , alternate_id |
| 405290898 | CV3197173 | single nucleotide variant | NM_018012.4(KIF26B):c.1735C>G (p.Leu579Val) | KIF26B-related disorder [RCV003984735] | benign | 1 | 245609349 | 245609349 | Human | | name , trait , alternate_id |
| 405275266 | CV3200069 | single nucleotide variant | NM_018012.4(KIF26B):c.1228G>C (p.Ala410Pro) | KIF26B-related disorder [RCV003974059] | benign | 1 | 245540828 | 245540828 | Human | | name , trait , alternate_id |
| 405292876 | CV3210433 | single nucleotide variant | NM_018012.4(KIF26B):c.2003A>G (p.Gln668Arg) | KIF26B-related disorder [RCV003931400] | likely benign | 1 | 245611881 | 245611881 | Human | | name , trait , alternate_id |
| 405278643 | CV3220298 | single nucleotide variant | NM_018012.4(KIF26B):c.2711G>A (p.Arg904Gln) | KIF26B-related disorder [RCV003976538] | benign | 1 | 245685694 | 245685694 | Human | | name , trait , alternate_id |
| 405293176 | CV3221251 | single nucleotide variant | NM_018012.4(KIF26B):c.1910C>T (p.Thr637Met) | KIF26B-related disorder [RCV003966783] | benign | 1 | 245609524 | 245609524 | Human | | name , trait , alternate_id |
| 405699001 | CV3227057 | single nucleotide variant | NM_018012.4(KIF26B):c.2233A>C (p.Asn745His) | not provided [RCV003993451] | uncertain significance | 1 | 245646255 | 245646255 | Human | | name |
| 405652399 | CV3268872 | single nucleotide variant | NM_018012.4(KIF26B):c.1020G>C (p.Glu340Asp) | not specified [RCV004414126] | uncertain significance | 1 | 245419599 | 245419599 | Human | | name |
| 405652401 | CV3268873 | single nucleotide variant | NM_018012.4(KIF26B):c.1190C>A (p.Ser397Tyr) | not specified [RCV004414127] | uncertain significance | 1 | 245540790 | 245540790 | Human | | name |
| 405652403 | CV3268874 | single nucleotide variant | NM_018012.4(KIF26B):c.1211G>A (p.Arg404Gln) | not specified [RCV004414128] | uncertain significance | 1 | 245540811 | 245540811 | Human | | name |
| 405652405 | CV3268875 | single nucleotide variant | NM_018012.4(KIF26B):c.2030G>A (p.Arg677His) | not specified [RCV004414129] | uncertain significance | 1 | 245611908 | 245611908 | Human | | name |
| 405652409 | CV3268877 | single nucleotide variant | NM_018012.4(KIF26B):c.2311C>T (p.Arg771Cys) | not specified [RCV004414131] | uncertain significance | 1 | 245684285 | 245684285 | Human | | name |
| 405652414 | CV3268879 | single nucleotide variant | NM_018012.4(KIF26B):c.2840T>C (p.Phe947Ser) | not specified [RCV004414133] | uncertain significance | 1 | 245685823 | 245685823 | Human | | name |
| 405652416 | CV3268880 | single nucleotide variant | NM_018012.4(KIF26B):c.2876C>A (p.Ala959Glu) | not specified [RCV004414134] | uncertain significance | 1 | 245685859 | 245685859 | Human | | name |
| 405652418 | CV3268881 | single nucleotide variant | NM_018012.4(KIF26B):c.2902G>A (p.Ala968Thr) | not specified [RCV004414135] | uncertain significance | 1 | 245685885 | 245685885 | Human | | name |
| 405652420 | CV3268882 | single nucleotide variant | NM_018012.4(KIF26B):c.2927A>G (p.Glu976Gly) | not specified [RCV004414136] | uncertain significance | 1 | 245685910 | 245685910 | Human | | name |
| 407525010 | CV3452128 | single nucleotide variant | NM_018012.4(KIF26B):c.2153C>T (p.Ala718Val) | not specified [RCV004631446] | uncertain significance | 1 | 245646175 | 245646175 | Human | | name |
| 407525006 | CV3452130 | single nucleotide variant | NM_018012.4(KIF26B):c.1991G>A (p.Arg664His) | not specified [RCV004631448] | uncertain significance | 1 | 245611869 | 245611869 | Human | | name |
| 407524803 | CV3452134 | single nucleotide variant | NM_018012.4(KIF26B):c.2519A>G (p.Asp840Gly) | not specified [RCV004631452] | uncertain significance | 1 | 245685502 | 245685502 | Human | | name |
| 407525044 | CV3452139 | single nucleotide variant | NM_018012.4(KIF26B):c.2887C>T (p.Pro963Ser) | not specified [RCV004631456] | uncertain significance | 1 | 245685870 | 245685870 | Human | | name |
| 407524660 | CV3452142 | single nucleotide variant | NM_018012.4(KIF26B):c.1810G>A (p.Glu604Lys) | not specified [RCV004631459] | uncertain significance | 1 | 245609424 | 245609424 | Human | | name |
| 407524672 | CV3452145 | single nucleotide variant | NM_018012.4(KIF26B):c.2596A>G (p.Ile866Val) | not specified [RCV004631462] | uncertain significance | 1 | 245685579 | 245685579 | Human | | name |
| 407495993 | CV3452151 | single nucleotide variant | NM_018012.4(KIF26B):c.2297G>A (p.Gly766Glu) | not specified [RCV004621700] | uncertain significance | 1 | 245684271 | 245684271 | Human | | name |
| 597630257 | CV3695136 | single nucleotide variant | NM_018012.4(KIF26B):c.2941G>T (p.Asp981Tyr) | not specified [RCV004939463] | uncertain significance | 1 | 245685924 | 245685924 | Human | | name |
| 597630298 | CV3695144 | single nucleotide variant | NM_018012.4(KIF26B):c.2227C>G (p.Leu743Val) | not specified [RCV004939470] | uncertain significance | 1 | 245646249 | 245646249 | Human | | name |
| 597630302 | CV3695145 | single nucleotide variant | NM_018012.4(KIF26B):c.2272G>T (p.Ala758Ser) | not specified [RCV004939471] | uncertain significance | 1 | 245684246 | 245684246 | Human | | name |
| 597630324 | CV3695149 | single nucleotide variant | NM_018012.4(KIF26B):c.1081G>A (p.Ala361Thr) | not specified [RCV004939475] | uncertain significance | 1 | 245419660 | 245419660 | Human | | name |
| 597630369 | CV3695158 | single nucleotide variant | NM_018012.4(KIF26B):c.2561A>G (p.Tyr854Cys) | not specified [RCV004939483] | uncertain significance | 1 | 245685544 | 245685544 | Human | | name |
| 597630147 | CV3698164 | single nucleotide variant | NM_018012.4(KIF26B):c.1234G>A (p.Glu412Lys) | not specified [RCV004939444] | uncertain significance | 1 | 245540834 | 245540834 | Human | | name |
| 597768100 | CV3698167 | single nucleotide variant | NM_018012.4(KIF26B):c.1150G>A (p.Ala384Thr) | not specified [RCV004927435] | uncertain significance | 1 | 245419729 | 245419729 | Human | | name |
| 597768110 | CV3698172 | single nucleotide variant | NM_018012.4(KIF26B):c.1748G>T (p.Arg583Leu) | not specified [RCV004927437] | uncertain significance | 1 | 245609362 | 245609362 | Human | | name |
| 597768115 | CV3698173 | single nucleotide variant | NM_018012.4(KIF26B):c.2710C>T (p.Arg904Trp) | not specified [RCV004927438] | uncertain significance | 1 | 245685693 | 245685693 | Human | | name |
| 597768136 | CV3698189 | single nucleotide variant | NM_018012.4(KIF26B):c.1429C>T (p.Arg477Trp) | not specified [RCV004927442] | uncertain significance | 1 | 245602655 | 245602655 | Human | | name |
| 598272503 | CV3990980 | single nucleotide variant | NM_018012.4(KIF26B):c.1835C>T (p.Ser612Leu) | not specified [RCV005350506] | uncertain significance | 1 | 245609449 | 245609449 | Human | | name |
| 598220460 | CV3990984 | single nucleotide variant | NM_018012.4(KIF26B):c.1400A>G (p.Glu467Gly) | not specified [RCV005360670] | uncertain significance | 1 | 245602626 | 245602626 | Human | | name |
| 598248419 | CV3990986 | single nucleotide variant | NM_018012.4(KIF26B):c.2399G>A (p.Arg800Lys) | not specified [RCV005366230] | uncertain significance | 1 | 245684373 | 245684373 | Human | | name |
| 598272511 | CV3990991 | single nucleotide variant | NM_018012.4(KIF26B):c.1430G>A (p.Arg477Gln) | not specified [RCV005350508] | uncertain significance | 1 | 245602656 | 245602656 | Human | | name |
| 598248434 | CV3990992 | single nucleotide variant | NM_018012.4(KIF26B):c.1840G>A (p.Val614Met) | not specified [RCV005366232] | uncertain significance | 1 | 245609454 | 245609454 | Human | | name |
| 598248441 | CV3990994 | single nucleotide variant | NM_018012.4(KIF26B):c.1042G>C (p.Glu348Gln) | not specified [RCV005366233] | uncertain significance | 1 | 245419621 | 245419621 | Human | | name |
| 598272522 | CV3990999 | single nucleotide variant | NM_018012.4(KIF26B):c.1802G>C (p.Trp601Ser) | not specified [RCV005350510] | uncertain significance | 1 | 245609416 | 245609416 | Human | | name |
| 15111476 | CV707262 | single nucleotide variant | NM_018012.4(KIF26B):c.2906C>T (p.Ala969Val) | KIF26B-related disorder [RCV003916041]|not provided [RCV000961114] | benign | 1 | 245685889 | 245685889 | Human | | name , trait , alternate_id |
| 15160851 | CV718844 | single nucleotide variant | NM_018012.4(KIF26B):c.1487A>G (p.Gln496Arg) | KIF26B-related disorder [RCV003910388]|not provided [RCV000881463] | likely benign | 1 | 245602713 | 245602713 | Human | | name , trait , alternate_id |
| 41407080 | CV980659 | single nucleotide variant | NM_018012.4(KIF26B):c.2110C>T (p.Arg704Cys) | not provided [RCV004799571]|not specified [RCV004035519] | uncertain significance | 1 | 245646132 | 245646132 | Human | | name |
| 156246740 | CV2196274 | single nucleotide variant | NM_018012.4(KIF26B):c.4654A>G (p.Ser1552Gly) | not specified [RCV004073623] | uncertain significance | 1 | 245687637 | 245687637 | Human | | name |
| 156082102 | CV2205409 | single nucleotide variant | NM_018012.4(KIF26B):c.4250G>T (p.Gly1417Val) | not specified [RCV004082354] | likely benign | 1 | 245687233 | 245687233 | Human | | name |
| 156326308 | CV2205690 | single nucleotide variant | NM_018012.4(KIF26B):c.3073G>A (p.Val1025Ile) | not specified [RCV004075753] | likely benign | 1 | 245686056 | 245686056 | Human | | name |
| 156334311 | CV2214748 | single nucleotide variant | NM_018012.4(KIF26B):c.3120C>G (p.Ser1040Arg) | not specified [RCV004090557] | uncertain significance | 1 | 245686103 | 245686103 | Human | | name |
| 156385222 | CV2227855 | single nucleotide variant | NM_018012.4(KIF26B):c.3559G>C (p.Glu1187Gln) | not specified [RCV004094494] | uncertain significance | 1 | 245686542 | 245686542 | Human | | name |
| 156130583 | CV2235171 | single nucleotide variant | NM_018012.4(KIF26B):c.5476G>A (p.Gly1826Arg) | not specified [RCV004107229] | uncertain significance | 1 | 245688459 | 245688459 | Human | | name |
| 156198705 | CV2237471 | single nucleotide variant | NM_018012.4(KIF26B):c.4171A>G (p.Ile1391Val) | not specified [RCV004106430] | uncertain significance | 1 | 245687154 | 245687154 | Human | | name |
| 156272003 | CV2247264 | single nucleotide variant | NM_018012.4(KIF26B):c.5900C>T (p.Thr1967Ile) | not specified [RCV004115042] | uncertain significance | 1 | 245698181 | 245698181 | Human | | name |
| 156088969 | CV2259092 | single nucleotide variant | NM_018012.4(KIF26B):c.4892C>T (p.Ala1631Val) | not specified [RCV004120348] | uncertain significance | 1 | 245687875 | 245687875 | Human | | name |
| 155973197 | CV2271618 | single nucleotide variant | NM_018012.4(KIF26B):c.5051G>A (p.Arg1684Gln) | not specified [RCV004599512] | uncertain significance | 1 | 245688034 | 245688034 | Human | | name |
| 156335821 | CV2273036 | single nucleotide variant | NM_018012.4(KIF26B):c.5608G>A (p.Asp1870Asn) | not specified [RCV004137689] | uncertain significance | 1 | 245688591 | 245688591 | Human | | name |
| 155920971 | CV2276226 | single nucleotide variant | NM_018012.4(KIF26B):c.3976G>A (p.Ala1326Thr) | not specified [RCV004142173] | uncertain significance | 1 | 245686959 | 245686959 | Human | | name |
| 156271232 | CV2286330 | single nucleotide variant | NM_018012.4(KIF26B):c.5492C>G (p.Ala1831Gly) | not specified [RCV004146277] | uncertain significance | 1 | 245688475 | 245688475 | Human | | name |
| 156261806 | CV2287535 | single nucleotide variant | NM_018012.4(KIF26B):c.3295C>G (p.Pro1099Ala) | not specified [RCV004140989] | uncertain significance | 1 | 245686278 | 245686278 | Human | | name |
| 156077406 | CV2291623 | single nucleotide variant | NM_018012.4(KIF26B):c.6088G>A (p.Glu2030Lys) | not specified [RCV004155914] | uncertain significance | 1 | 245698947 | 245698947 | Human | | name |
| 156344615 | CV2294156 | single nucleotide variant | NM_018012.4(KIF26B):c.4727C>T (p.Thr1576Ile) | not specified [RCV004149523] | uncertain significance | 1 | 245687710 | 245687710 | Human | | name |
| 156144141 | CV2296481 | single nucleotide variant | NM_018012.4(KIF26B):c.4195A>C (p.Met1399Leu) | not specified [RCV004148218] | uncertain significance | 1 | 245687178 | 245687178 | Human | | name |
| 156348467 | CV2312812 | single nucleotide variant | NM_018012.4(KIF26B):c.3374G>A (p.Arg1125His) | not specified [RCV004171313] | uncertain significance | 1 | 245686357 | 245686357 | Human | | name |
| 156046206 | CV2315585 | single nucleotide variant | NM_018012.4(KIF26B):c.4605C>G (p.Ser1535Arg) | not specified [RCV004169626] | uncertain significance | 1 | 245687588 | 245687588 | Human | | name |
| 156049074 | CV2315821 | single nucleotide variant | NM_018012.4(KIF26B):c.5227C>T (p.Pro1743Ser) | not specified [RCV004171602] | uncertain significance | 1 | 245688210 | 245688210 | Human | | name |
| 156272272 | CV2315911 | single nucleotide variant | NM_018012.4(KIF26B):c.3047G>C (p.Ser1016Thr) | not specified [RCV004171679] | uncertain significance | 1 | 245686030 | 245686030 | Human | | name |
| 156174841 | CV2327013 | single nucleotide variant | NM_018012.4(KIF26B):c.5521C>A (p.Pro1841Thr) | not specified [RCV004178603] | uncertain significance | 1 | 245688504 | 245688504 | Human | | name |
| 156077302 | CV2331869 | single nucleotide variant | NM_018012.4(KIF26B):c.3742G>A (p.Val1248Ile) | not specified [RCV004186525] | uncertain significance | 1 | 245686725 | 245686725 | Human | | name |
| 155968232 | CV2337820 | single nucleotide variant | NM_018012.4(KIF26B):c.4576G>T (p.Val1526Leu) | not specified [RCV004183832] | uncertain significance | 1 | 245687559 | 245687559 | Human | | name |
| 156217704 | CV2348175 | single nucleotide variant | NM_018012.4(KIF26B):c.5996G>A (p.Arg1999His) | not specified [RCV004190818] | uncertain significance | 1 | 245698277 | 245698277 | Human | | name |
| 156284277 | CV2349009 | single nucleotide variant | NM_018012.4(KIF26B):c.3860C>T (p.Ala1287Val) | not specified [RCV004203435] | uncertain significance | 1 | 245686843 | 245686843 | Human | | name |
| 155990546 | CV2352485 | single nucleotide variant | NM_018012.4(KIF26B):c.4636C>T (p.Arg1546Trp) | not specified [RCV004202989] | uncertain significance | 1 | 245687619 | 245687619 | Human | | name |
| 155925100 | CV2358270 | single nucleotide variant | NM_018012.4(KIF26B):c.5291C>T (p.Pro1764Leu) | not specified [RCV004212058] | uncertain significance | 1 | 245688274 | 245688274 | Human | | name |
| 156250237 | CV2359062 | single nucleotide variant | NM_018012.4(KIF26B):c.5306A>G (p.Gln1769Arg) | not specified [RCV004212384] | uncertain significance | 1 | 245688289 | 245688289 | Human | | name |
| 155927076 | CV2365867 | single nucleotide variant | NM_018012.4(KIF26B):c.4966A>G (p.Ser1656Gly) | not specified [RCV004214396] | uncertain significance | 1 | 245687949 | 245687949 | Human | | name |
| 156342667 | CV2368595 | single nucleotide variant | NM_018012.4(KIF26B):c.3346A>G (p.Arg1116Gly) | not specified [RCV004221379] | uncertain significance | 1 | 245686329 | 245686329 | Human | | name |
| 156388879 | CV2376181 | single nucleotide variant | NM_018012.4(KIF26B):c.4220C>T (p.Pro1407Leu) | not specified [RCV004220407] | uncertain significance | 1 | 245687203 | 245687203 | Human | | name |
| 156049392 | CV2378208 | single nucleotide variant | NM_018012.4(KIF26B):c.3427G>A (p.Gly1143Arg) | not specified [RCV004226249] | uncertain significance | 1 | 245686410 | 245686410 | Human | | name |
| 156045628 | CV2381730 | single nucleotide variant | NM_018012.4(KIF26B):c.3905C>T (p.Thr1302Met) | not specified [RCV004232186] | uncertain significance | 1 | 245686888 | 245686888 | Human | | name |
| 156390551 | CV2383207 | single nucleotide variant | NM_018012.4(KIF26B):c.6044A>G (p.Asn2015Ser) | not specified [RCV004220217] | uncertain significance | 1 | 245698903 | 245698903 | Human | | name |
| 156265528 | CV2389070 | single nucleotide variant | NM_018012.4(KIF26B):c.3265T>G (p.Cys1089Gly) | not specified [RCV004235408] | uncertain significance | 1 | 245686248 | 245686248 | Human | | name |
| 155927395 | CV2391320 | single nucleotide variant | NM_018012.4(KIF26B):c.6259C>T (p.Arg2087Cys) | not specified [RCV004237682] | uncertain significance | 1 | 245702538 | 245702538 | Human | | name |
| 156256396 | CV2397767 | single nucleotide variant | NM_018012.4(KIF26B):c.3367G>A (p.Glu1123Lys) | not specified [RCV004239244] | uncertain significance | 1 | 245686350 | 245686350 | Human | | name |
| 155996349 | CV2398526 | single nucleotide variant | NM_018012.4(KIF26B):c.4501C>T (p.Pro1501Ser) | not specified [RCV004237845] | uncertain significance | 1 | 245687484 | 245687484 | Human | | name |
| 156004636 | CV2401007 | single nucleotide variant | NM_018012.4(KIF26B):c.5780G>A (p.Gly1927Asp) | not specified [RCV004244286] | uncertain significance | 1 | 245688763 | 245688763 | Human | | name |
| 329368091 | CV2424181 | single nucleotide variant | NM_018012.4(KIF26B):c.3412A>C (p.Lys1138Gln) | not specified [RCV004250309] | uncertain significance | 1 | 245686395 | 245686395 | Human | | name |
| 329367740 | CV2427534 | single nucleotide variant | NM_018012.4(KIF26B):c.3118A>T (p.Ser1040Cys) | not specified [RCV004250172] | uncertain significance | 1 | 245686101 | 245686101 | Human | | name |
| 329358068 | CV2427932 | single nucleotide variant | NM_018012.4(KIF26B):c.3353C>A (p.Ser1118Tyr) | not specified [RCV004254320] | uncertain significance | 1 | 245686336 | 245686336 | Human | | name |
| 329365073 | CV2440013 | single nucleotide variant | NM_018012.4(KIF26B):c.5410G>A (p.Val1804Ile) | not specified [RCV004260487] | uncertain significance | 1 | 245688393 | 245688393 | Human | | name |
| 329355503 | CV2445509 | single nucleotide variant | NM_018012.4(KIF26B):c.5935A>G (p.Ser1979Gly) | not specified [RCV004257565] | uncertain significance | 1 | 245698216 | 245698216 | Human | | name |
| 329397852 | CV2464077 | single nucleotide variant | NM_018012.4(KIF26B):c.4265A>C (p.Gln1422Pro) | not specified [RCV004273775] | uncertain significance | 1 | 245687248 | 245687248 | Human | | name |
| 329401959 | CV2467700 | single nucleotide variant | NM_018012.4(KIF26B):c.6242C>T (p.Thr2081Met) | not specified [RCV004281318] | uncertain significance | 1 | 245702521 | 245702521 | Human | | name |
| 401730554 | CV2677221 | single nucleotide variant | NM_018012.4(KIF26B):c.5326G>A (p.Gly1776Ser) | not specified [RCV004295845] | likely benign | 1 | 245688309 | 245688309 | Human | | name |
| 401767557 | CV2681702 | single nucleotide variant | NM_018012.4(KIF26B):c.3748G>A (p.Glu1250Lys) | not specified [RCV004294251] | uncertain significance | 1 | 245686731 | 245686731 | Human | | name |
| 401733467 | CV2682122 | single nucleotide variant | NM_018012.4(KIF26B):c.4918G>C (p.Glu1640Gln) | not specified [RCV004290177] | uncertain significance | 1 | 245687901 | 245687901 | Human | | name |
| 401725856 | CV2687311 | single nucleotide variant | NM_018012.4(KIF26B):c.5308G>A (p.Gly1770Ser) | not specified [RCV004298245] | likely benign | 1 | 245688291 | 245688291 | Human | | name |
| 401744539 | CV2688184 | single nucleotide variant | NM_018012.4(KIF26B):c.4769C>T (p.Ala1590Val) | not specified [RCV004305227] | uncertain significance | 1 | 245687752 | 245687752 | Human | | name |
| 401745785 | CV2693349 | single nucleotide variant | NM_018012.4(KIF26B):c.3320C>T (p.Ser1107Leu) | not specified [RCV004295312] | likely benign | 1 | 245686303 | 245686303 | Human | | name |
| 401748020 | CV2698910 | single nucleotide variant | NM_018012.4(KIF26B):c.5026C>A (p.His1676Asn) | not specified [RCV004303453] | uncertain significance | 1 | 245688009 | 245688009 | Human | | name |
| 401762161 | CV2699541 | single nucleotide variant | NM_018012.4(KIF26B):c.4064C>T (p.Ala1355Val) | not specified [RCV004299748] | uncertain significance | 1 | 245687047 | 245687047 | Human | | name |
| 401736836 | CV2699610 | single nucleotide variant | NM_018012.4(KIF26B):c.4663T>C (p.Tyr1555His) | not specified [RCV004299798] | uncertain significance | 1 | 245687646 | 245687646 | Human | | name |
| 401734409 | CV2709490 | single nucleotide variant | NM_018012.4(KIF26B):c.4292C>T (p.Ala1431Val) | not specified [RCV004318733] | uncertain significance | 1 | 245687275 | 245687275 | Human | | name |
| 401742654 | CV2715285 | single nucleotide variant | NM_018012.4(KIF26B):c.4528G>A (p.Val1510Met) | not specified [RCV004324624] | uncertain significance | 1 | 245687511 | 245687511 | Human | | name |
| 401765576 | CV2725240 | single nucleotide variant | NM_018012.4(KIF26B):c.3685G>A (p.Val1229Ile) | not specified [RCV004321754] | uncertain significance | 1 | 245686668 | 245686668 | Human | | name |
| 401768668 | CV2735386 | single nucleotide variant | NM_018012.4(KIF26B):c.4723G>A (p.Ala1575Thr) | not specified [RCV004334039] | uncertain significance | 1 | 245687706 | 245687706 | Human | | name |
| 401875155 | CV2756258 | single nucleotide variant | NM_018012.4(KIF26B):c.3779C>T (p.Pro1260Leu) | not specified [RCV004338353] | uncertain significance | 1 | 245686762 | 245686762 | Human | | name |
| 401862459 | CV2762113 | single nucleotide variant | NM_018012.4(KIF26B):c.5531C>T (p.Ala1844Val) | not specified [RCV004341929] | uncertain significance | 1 | 245688514 | 245688514 | Human | | name |
| 401863188 | CV2765577 | single nucleotide variant | NM_018012.4(KIF26B):c.4690G>T (p.Val1564Leu) | not specified [RCV004335594] | uncertain significance | 1 | 245687673 | 245687673 | Human | | name |
| 401894025 | CV2770236 | single nucleotide variant | NM_018012.4(KIF26B):c.5414G>A (p.Ser1805Asn) | not specified [RCV004356125] | likely benign | 1 | 245688397 | 245688397 | Human | | name |
| 401898970 | CV2792170 | single nucleotide variant | NM_018012.4(KIF26B):c.3614G>T (p.Gly1205Val) | not specified [RCV004361380] | uncertain significance | 1 | 245686597 | 245686597 | Human | | name |
| 401937163 | CV2812923 | single nucleotide variant | NM_018012.4(KIF26B):c.4064C>G (p.Ala1355Gly) | not provided [RCV003415103] | likely benign | 1 | 245687047 | 245687047 | Human | | name |
| 405283642 | CV3191777 | single nucleotide variant | NM_018012.4(KIF26B):c.3187A>G (p.Met1063Val) | KIF26B-related disorder [RCV003921877] | likely benign | 1 | 245686170 | 245686170 | Human | | name , trait , alternate_id |
| 405286697 | CV3192231 | single nucleotide variant | NM_018012.4(KIF26B):c.3304G>A (p.Ala1102Thr) | KIF26B-related disorder [RCV003924133]|not specified [RCV005363316] | likely benign|uncertain significance | 1 | 245686287 | 245686287 | Human | | name , trait , alternate_id |
| 405276942 | CV3192305 | single nucleotide variant | NM_018012.4(KIF26B):c.3572C>T (p.Thr1191Met) | KIF26B-related disorder [RCV003917279] | benign | 1 | 245686555 | 245686555 | Human | | name , trait , alternate_id |
| 405292442 | CV3192446 | single nucleotide variant | NM_018012.4(KIF26B):c.5836C>T (p.Arg1946Trp) | KIF26B-related disorder [RCV003929711] | benign | 1 | 245698117 | 245698117 | Human | | name , trait , alternate_id |
| 405266669 | CV3202002 | single nucleotide variant | NM_018012.4(KIF26B):c.5525C>A (p.Ala1842Glu) | KIF26B-related disorder [RCV003911485] | benign | 1 | 245688508 | 245688508 | Human | | name , trait , alternate_id |
| 405293140 | CV3207232 | single nucleotide variant | NM_018012.4(KIF26B):c.3653C>T (p.Ser1218Phe) | KIF26B-related disorder [RCV003931630] | likely benign | 1 | 245686636 | 245686636 | Human | | name , trait , alternate_id |
| 405285282 | CV3212330 | single nucleotide variant | NM_018012.4(KIF26B):c.5165G>C (p.Gly1722Ala) | KIF26B-related disorder [RCV003958948] | benign | 1 | 245688148 | 245688148 | Human | | name , trait , alternate_id |
| 405283046 | CV3216912 | single nucleotide variant | NM_018012.4(KIF26B):c.5324C>G (p.Pro1775Arg) | KIF26B-related disorder [RCV003979075] | benign | 1 | 245688307 | 245688307 | Human | | name , trait , alternate_id |
| 405271610 | CV3219093 | single nucleotide variant | NM_018012.4(KIF26B):c.6008G>A (p.Arg2003Gln) | KIF26B-related disorder [RCV003971800] | likely benign | 1 | 245698289 | 245698289 | Human | | name , trait , alternate_id |
| 405652427 | CV3268885 | single nucleotide variant | NM_018012.4(KIF26B):c.3383C>T (p.Pro1128Leu) | not specified [RCV004414139] | uncertain significance | 1 | 245686366 | 245686366 | Human | | name |
| 405652429 | CV3268886 | single nucleotide variant | NM_018012.4(KIF26B):c.3616C>T (p.Arg1206Cys) | not specified [RCV004414140] | uncertain significance | 1 | 245686599 | 245686599 | Human | | name |
| 405652431 | CV3268887 | single nucleotide variant | NM_018012.4(KIF26B):c.3928A>G (p.Met1310Val) | not specified [RCV004414141] | uncertain significance | 1 | 245686911 | 245686911 | Human | | name |
| 405652433 | CV3268888 | single nucleotide variant | NM_018012.4(KIF26B):c.4012G>T (p.Asp1338Tyr) | not specified [RCV004414142] | uncertain significance | 1 | 245686995 | 245686995 | Human | | name |
| 405652435 | CV3268889 | single nucleotide variant | NM_018012.4(KIF26B):c.4057A>C (p.Lys1353Gln) | not specified [RCV004414143] | uncertain significance | 1 | 245687040 | 245687040 | Human | | name |
| 405652437 | CV3268890 | single nucleotide variant | NM_018012.4(KIF26B):c.4219C>T (p.Pro1407Ser) | not specified [RCV004414144] | uncertain significance | 1 | 245687202 | 245687202 | Human | | name |
| 405652439 | CV3268891 | single nucleotide variant | NM_018012.4(KIF26B):c.4372G>A (p.Glu1458Lys) | not specified [RCV004414145] | uncertain significance | 1 | 245687355 | 245687355 | Human | | name |
| 405652441 | CV3268892 | single nucleotide variant | NM_018012.4(KIF26B):c.4499C>A (p.Ser1500Tyr) | not specified [RCV004414146] | uncertain significance | 1 | 245687482 | 245687482 | Human | | name |
| 405652491 | CV3268894 | single nucleotide variant | NM_018012.4(KIF26B):c.4831C>T (p.Arg1611Trp) | not specified [RCV004414148] | uncertain significance | 1 | 245687814 | 245687814 | Human | | name |
| 405652494 | CV3268895 | single nucleotide variant | NM_018012.4(KIF26B):c.4844A>G (p.Gln1615Arg) | not specified [RCV004414149] | uncertain significance | 1 | 245687827 | 245687827 | Human | | name |
| 405652496 | CV3268896 | single nucleotide variant | NM_018012.4(KIF26B):c.4901C>G (p.Pro1634Arg) | not specified [RCV004414150] | uncertain significance | 1 | 245687884 | 245687884 | Human | | name |
| 405652500 | CV3268898 | single nucleotide variant | NM_018012.4(KIF26B):c.5109G>T (p.Met1703Ile) | not specified [RCV004414152] | uncertain significance | 1 | 245688092 | 245688092 | Human | | name |
| 405652502 | CV3268899 | single nucleotide variant | NM_018012.4(KIF26B):c.5120G>C (p.Gly1707Ala) | not specified [RCV004414153] | uncertain significance | 1 | 245688103 | 245688103 | Human | | name |
| 405652505 | CV3268900 | single nucleotide variant | NM_018012.4(KIF26B):c.5124G>T (p.Arg1708Ser) | not specified [RCV004414154] | uncertain significance | 1 | 245688107 | 245688107 | Human | | name |
| 405652507 | CV3268901 | single nucleotide variant | NM_018012.4(KIF26B):c.5225G>A (p.Ser1742Asn) | not specified [RCV004414155] | uncertain significance | 1 | 245688208 | 245688208 | Human | | name |
| 405652509 | CV3268902 | single nucleotide variant | NM_018012.4(KIF26B):c.5234C>T (p.Ala1745Val) | not specified [RCV004414156] | uncertain significance | 1 | 245688217 | 245688217 | Human | | name |
| 405652511 | CV3268903 | single nucleotide variant | NM_018012.4(KIF26B):c.5297C>T (p.Ala1766Val) | not specified [RCV004414157] | uncertain significance | 1 | 245688280 | 245688280 | Human | | name |
| 405652512 | CV3268904 | single nucleotide variant | NM_018012.4(KIF26B):c.5525C>T (p.Ala1842Val) | not specified [RCV004414158] | uncertain significance | 1 | 245688508 | 245688508 | Human | | name |
| 405652514 | CV3268905 | single nucleotide variant | NM_018012.4(KIF26B):c.5677G>A (p.Gly1893Ser) | not specified [RCV004414159] | uncertain significance | 1 | 245688660 | 245688660 | Human | | name |
| 405652518 | CV3268907 | single nucleotide variant | NM_018012.4(KIF26B):c.5755A>C (p.Ser1919Arg) | not specified [RCV004414161] | uncertain significance | 1 | 245688738 | 245688738 | Human | | name |
| 405652520 | CV3268908 | single nucleotide variant | NM_018012.4(KIF26B):c.5905G>A (p.Val1969Ile) | not specified [RCV004414162] | uncertain significance | 1 | 245698186 | 245698186 | Human | | name |
| 405652522 | CV3268909 | single nucleotide variant | NM_018012.4(KIF26B):c.6050A>G (p.Lys2017Arg) | not specified [RCV004414163] | uncertain significance | 1 | 245698909 | 245698909 | Human | | name |
| 407525008 | CV3452129 | single nucleotide variant | NM_018012.4(KIF26B):c.5543C>T (p.Pro1848Leu) | not specified [RCV004631447] | uncertain significance | 1 | 245688526 | 245688526 | Human | | name |
| 407525003 | CV3452131 | single nucleotide variant | NM_018012.4(KIF26B):c.4012G>A (p.Asp1338Asn) | not specified [RCV004631449] | uncertain significance | 1 | 245686995 | 245686995 | Human | | name |
| 407524729 | CV3452135 | single nucleotide variant | NM_018012.4(KIF26B):c.3737C>G (p.Ala1246Gly) | not specified [RCV004631453] | uncertain significance | 1 | 245686720 | 245686720 | Human | | name |
| 407495990 | CV3452136 | single nucleotide variant | NM_018012.4(KIF26B):c.6023G>A (p.Ser2008Asn) | not specified [RCV004621699] | uncertain significance | 1 | 245698304 | 245698304 | Human | | name |
| 407524648 | CV3452138 | single nucleotide variant | NM_018012.4(KIF26B):c.4331G>A (p.Arg1444Gln) | not specified [RCV004631455] | uncertain significance | 1 | 245687314 | 245687314 | Human | | name |
| 407524654 | CV3452140 | single nucleotide variant | NM_018012.4(KIF26B):c.3191G>C (p.Gly1064Ala) | not specified [RCV004631457] | uncertain significance | 1 | 245686174 | 245686174 | Human | | name |
| 407524657 | CV3452141 | single nucleotide variant | NM_018012.4(KIF26B):c.5971G>C (p.Val1991Leu) | not specified [RCV004631458] | uncertain significance | 1 | 245698252 | 245698252 | Human | | name |
| 407524667 | CV3452144 | single nucleotide variant | NM_018012.4(KIF26B):c.4082A>T (p.Lys1361Ile) | not specified [RCV004631461] | uncertain significance | 1 | 245687065 | 245687065 | Human | | name |
| 407524675 | CV3452146 | single nucleotide variant | NM_018012.4(KIF26B):c.5221G>T (p.Ala1741Ser) | not specified [RCV004631463] | uncertain significance | 1 | 245688204 | 245688204 | Human | | name |
| 407524678 | CV3452147 | single nucleotide variant | NM_018012.4(KIF26B):c.4917C>G (p.Asp1639Glu) | not specified [RCV004631464] | uncertain significance | 1 | 245687900 | 245687900 | Human | | name |
| 407524681 | CV3452148 | single nucleotide variant | NM_018012.4(KIF26B):c.3245C>T (p.Pro1082Leu) | not specified [RCV004631465] | uncertain significance | 1 | 245686228 | 245686228 | Human | | name |
| 407524691 | CV3452152 | single nucleotide variant | NM_018012.4(KIF26B):c.5983G>A (p.Asp1995Asn) | not specified [RCV004631468] | uncertain significance | 1 | 245698264 | 245698264 | Human | | name |
| 597630264 | CV3695137 | single nucleotide variant | NM_018012.4(KIF26B):c.5059A>T (p.Ser1687Cys) | not specified [RCV004939464] | uncertain significance | 1 | 245688042 | 245688042 | Human | | name |
| 597630269 | CV3695138 | single nucleotide variant | NM_018012.4(KIF26B):c.3140G>A (p.Arg1047Gln) | not specified [RCV004939465] | uncertain significance | 1 | 245686123 | 245686123 | Human | | name |
| 597768146 | CV3695143 | single nucleotide variant | NM_018012.4(KIF26B):c.4697C>T (p.Ala1566Val) | not specified [RCV004927444] | uncertain significance | 1 | 245687680 | 245687680 | Human | | name |
| 597630307 | CV3695146 | single nucleotide variant | NM_018012.4(KIF26B):c.4487A>T (p.Glu1496Val) | not specified [RCV004939472] | uncertain significance | 1 | 245687470 | 245687470 | Human | | name |
| 597630318 | CV3695148 | single nucleotide variant | NM_018012.4(KIF26B):c.4373A>G (p.Glu1458Gly) | not specified [RCV004939474] | uncertain significance | 1 | 245687356 | 245687356 | Human | | name |
| 597630347 | CV3695154 | single nucleotide variant | NM_018012.4(KIF26B):c.5795T>C (p.Leu1932Pro) | not specified [RCV004939479] | uncertain significance | 1 | 245688778 | 245688778 | Human | | name |
| 597630364 | CV3695157 | single nucleotide variant | NM_018012.4(KIF26B):c.5014G>T (p.Ala1672Ser) | not specified [RCV004939482] | uncertain significance | 1 | 245687997 | 245687997 | Human | | name |
| 597630376 | CV3695159 | single nucleotide variant | NM_018012.4(KIF26B):c.4468C>G (p.Leu1490Val) | not specified [RCV004939484] | uncertain significance | 1 | 245687451 | 245687451 | Human | | name |
| 597768095 | CV3698165 | single nucleotide variant | NM_018012.4(KIF26B):c.4520G>A (p.Arg1507Lys) | not specified [RCV004927434] | uncertain significance | 1 | 245687503 | 245687503 | Human | | name |
| 597768106 | CV3698168 | single nucleotide variant | NM_018012.4(KIF26B):c.3166G>A (p.Val1056Met) | not specified [RCV004927436] | likely benign | 1 | 245686149 | 245686149 | Human | | name |
| 597630159 | CV3698169 | single nucleotide variant | NM_018012.4(KIF26B):c.6323G>A (p.Arg2108Gln) | not specified [RCV004939446] | uncertain significance | 1 | 245702602 | 245702602 | Human | | name |
| 597630165 | CV3698170 | single nucleotide variant | NM_018012.4(KIF26B):c.6094C>T (p.Arg2032Cys) | not specified [RCV004939447] | uncertain significance | 1 | 245698953 | 245698953 | Human | | name |
| 597630172 | CV3698171 | single nucleotide variant | NM_018012.4(KIF26B):c.4400C>T (p.Thr1467Met) | not specified [RCV004939448] | uncertain significance | 1 | 245687383 | 245687383 | Human | | name |
| 597630178 | CV3698174 | single nucleotide variant | NM_018012.4(KIF26B):c.3671C>T (p.Ser1224Leu) | not specified [RCV004939449] | uncertain significance | 1 | 245686654 | 245686654 | Human | | name |
| 597630183 | CV3698175 | single nucleotide variant | NM_018012.4(KIF26B):c.5248G>A (p.Ala1750Thr) | not specified [RCV004939450] | likely benign | 1 | 245688231 | 245688231 | Human | | name |
| 597630201 | CV3698180 | single nucleotide variant | NM_018012.4(KIF26B):c.3230C>T (p.Ser1077Leu) | not specified [RCV004939453] | uncertain significance | 1 | 245686213 | 245686213 | Human | | name |
| 597630206 | CV3698181 | single nucleotide variant | NM_018012.4(KIF26B):c.3559G>A (p.Glu1187Lys) | not specified [RCV004939454] | uncertain significance | 1 | 245686542 | 245686542 | Human | | name |
| 597630211 | CV3698182 | single nucleotide variant | NM_018012.4(KIF26B):c.4105A>G (p.Met1369Val) | not specified [RCV004939455] | uncertain significance | 1 | 245687088 | 245687088 | Human | | name |
| 597630217 | CV3698183 | single nucleotide variant | NM_018012.4(KIF26B):c.6320G>A (p.Arg2107His) | not specified [RCV004939456] | uncertain significance | 1 | 245702599 | 245702599 | Human | | name |
| 597630240 | CV3698187 | single nucleotide variant | NM_018012.4(KIF26B):c.3473C>G (p.Ala1158Gly) | not specified [RCV004939460] | uncertain significance | 1 | 245686456 | 245686456 | Human | | name |
| 597768132 | CV3698188 | single nucleotide variant | NM_018012.4(KIF26B):c.4904C>T (p.Ala1635Val) | not specified [RCV004927441] | uncertain significance | 1 | 245687887 | 245687887 | Human | | name |
| 597630245 | CV3698190 | single nucleotide variant | NM_018012.4(KIF26B):c.3515C>T (p.Thr1172Met) | not specified [RCV004939461] | uncertain significance | 1 | 245686498 | 245686498 | Human | | name |
| 597630251 | CV3698191 | single nucleotide variant | NM_018012.4(KIF26B):c.4988C>A (p.Ala1663Asp) | not specified [RCV004939462] | uncertain significance | 1 | 245687971 | 245687971 | Human | | name |
| 597768140 | CV3698192 | single nucleotide variant | NM_018012.4(KIF26B):c.3239A>G (p.Lys1080Arg) | not specified [RCV004927443] | uncertain significance | 1 | 245686222 | 245686222 | Human | | name |
| 598248383 | CV3990977 | single nucleotide variant | NM_018012.4(KIF26B):c.6011G>A (p.Arg2004Gln) | not specified [RCV005366225] | uncertain significance | 1 | 245698292 | 245698292 | Human | | name |
| 598248388 | CV3990978 | single nucleotide variant | NM_018012.4(KIF26B):c.4403G>A (p.Gly1468Asp) | not specified [RCV005366226] | uncertain significance | 1 | 245687386 | 245687386 | Human | | name |
| 598248396 | CV3990981 | single nucleotide variant | NM_018012.4(KIF26B):c.3116A>G (p.Gln1039Arg) | not specified [RCV005366227] | uncertain significance | 1 | 245686099 | 245686099 | Human | | name |
| 598248404 | CV3990982 | single nucleotide variant | NM_018012.4(KIF26B):c.3811G>A (p.Ala1271Thr) | not specified [RCV005366228] | uncertain significance | 1 | 245686794 | 245686794 | Human | | name |
| 598220468 | CV3990985 | single nucleotide variant | NM_018012.4(KIF26B):c.5003C>T (p.Ser1668Leu) | not specified [RCV005360671] | uncertain significance | 1 | 245687986 | 245687986 | Human | | name |
| 598248426 | CV3990990 | single nucleotide variant | NM_018012.4(KIF26B):c.3437G>A (p.Gly1146Glu) | not specified [RCV005366231] | uncertain significance | 1 | 245686420 | 245686420 | Human | | name |
| 598220488 | CV3990993 | single nucleotide variant | NM_018012.4(KIF26B):c.4733A>T (p.Glu1578Val) | not specified [RCV005360674] | uncertain significance | 1 | 245687716 | 245687716 | Human | | name |
| 598248450 | CV3990995 | single nucleotide variant | NM_018012.4(KIF26B):c.3662C>T (p.Ala1221Val) | not specified [RCV005366234] | uncertain significance | 1 | 245686645 | 245686645 | Human | | name |
| 598220494 | CV3990996 | single nucleotide variant | NM_018012.4(KIF26B):c.5558A>C (p.Lys1853Thr) | not specified [RCV005360675] | uncertain significance | 1 | 245688541 | 245688541 | Human | | name |
| 598272516 | CV3990997 | single nucleotide variant | NM_018012.4(KIF26B):c.3688A>C (p.Ser1230Arg) | not specified [RCV005350509] | uncertain significance | 1 | 245686671 | 245686671 | Human | | name |
| 598248457 | CV3990998 | single nucleotide variant | NM_018012.4(KIF26B):c.5452G>A (p.Ala1818Thr) | not specified [RCV005366235] | uncertain significance | 1 | 245688435 | 245688435 | Human | | name |
| 616940040 | CV4014234 | single nucleotide variant | NM_018012.4(KIF26B):c.6106G>C (p.Glu2036Gln) | not provided [RCV005413727] | uncertain significance | 1 | 245698965 | 245698965 | Human | | name |
| 13462947 | CV439676 | single nucleotide variant | NM_018012.4(KIF26B):c.5710G>A (p.Asp1904Asn) | Autosomal dominant cerebellar ataxia [RCV001849185]|not provided [RCV000515515] | pathogenic|uncertain significance | 1 | 245688693 | 245688693 | Human | 1 | name |
| 15155871 | CV696634 | single nucleotide variant | NM_018012.4(KIF26B):c.4325T>G (p.Leu1442Arg) | KIF26B-related disorder [RCV003960584]|not provided [RCV000946581] | benign | 1 | 245687308 | 245687308 | Human | | name , trait , alternate_id |
| 15172671 | CV696635 | single nucleotide variant | NM_018012.4(KIF26B):c.4703C>T (p.Ser1568Leu) | KIF26B-related disorder [RCV003978206]|not provided [RCV000950077] | benign|likely benign | 1 | 245687686 | 245687686 | Human | | name , trait , alternate_id |
| 15103682 | CV696637 | single nucleotide variant | NM_018012.4(KIF26B):c.6131C>T (p.Ala2044Val) | KIF26B-related disorder [RCV003926105]|not provided [RCV000959530] | benign | 1 | 245698990 | 245698990 | Human | | name , trait , alternate_id |
| 15112883 | CV707265 | single nucleotide variant | NM_018012.4(KIF26B):c.4084A>G (p.Ile1362Val) | KIF26B-related disorder [RCV003970831]|not provided [RCV000961382] | benign|likely benign | 1 | 245687067 | 245687067 | Human | | name , trait , alternate_id |
| 15161331 | CV707266 | single nucleotide variant | NM_018012.4(KIF26B):c.4228C>G (p.Pro1410Ala) | KIF26B-related disorder [RCV003928477]|not provided [RCV000970069] | likely benign | 1 | 245687211 | 245687211 | Human | | name , trait , alternate_id |
| 15196844 | CV718846 | single nucleotide variant | NM_018012.4(KIF26B):c.3457G>A (p.Asp1153Asn) | not provided [RCV000889885] | likely benign | 1 | 245686440 | 245686440 | Human | | name |
| 15151228 | CV718847 | single nucleotide variant | NM_018012.4(KIF26B):c.3881C>T (p.Ser1294Leu) | KIF26B-related disorder [RCV003955794]|not provided [RCV000879551] | likely benign | 1 | 245686864 | 245686864 | Human | | name , trait , alternate_id |
| 15104935 | CV718851 | single nucleotide variant | NM_018012.4(KIF26B):c.5131G>A (p.Gly1711Ser) | KIF26B-related disorder [RCV003940729]|not provided [RCV000892983] | benign | 1 | 245688114 | 245688114 | Human | | name , trait , alternate_id |
| 15191687 | CV718852 | single nucleotide variant | NM_018012.4(KIF26B):c.5200G>A (p.Ala1734Thr) | KIF26B-related disorder [RCV003910524]|not provided [RCV000888449] | benign | 1 | 245688183 | 245688183 | Human | | name , trait , alternate_id |
| 9831571 | CV166635 | deletion | NM_018012.4(KIF26B):c.1166+53868_1166+59172del | Preeclampsia [RCV000161201] | not provided | 1 | 245473613 | 245478917 | Human | | name |
| 11542457 | CV213936 | deletion | NM_018012.4(KIF26B):c.5146_5167del (p.Thr1716fs) | not provided [RCV000240638] | pathogenic | 1 | 245688126 | 245688147 | Human | | name |
