| 156273076 | CV2202449 | single nucleotide variant | NM_198285.3(WDR86):c.97G>A (p.Gly33Ser) | not specified [RCV004080755] | uncertain significance | 7 | 151409493 | 151409493 | Human | | name |
| 401742627 | CV2677640 | single nucleotide variant | NM_198285.3(WDR86):c.46G>A (p.Gly16Arg) | not specified [RCV004291729] | uncertain significance | 7 | 151409544 | 151409544 | Human | | name |
| 401884819 | CV2766263 | single nucleotide variant | NM_198285.3(WDR86):c.56A>T (p.Asn19Ile) | not specified [RCV004342519] | uncertain significance | 7 | 151409534 | 151409534 | Human | | name |
| 405807548 | CV3356477 | single nucleotide variant | NM_198285.3(WDR86):c.92T>A (p.Leu31Gln) | not specified [RCV004480737] | uncertain significance | 7 | 151409498 | 151409498 | Human | | name |
| 156270430 | CV2195163 | single nucleotide variant | NM_198285.3(WDR86):c.259G>A (p.Gly87Arg) | not specified [RCV004080111] | uncertain significance | 7 | 151400146 | 151400146 | Human | | name |
| 156192151 | CV2206237 | single nucleotide variant | NM_198285.3(WDR86):c.290C>T (p.Thr97Met) | not specified [RCV004080669] | uncertain significance | 7 | 151400115 | 151400115 | Human | | name |
| 155920791 | CV2279650 | single nucleotide variant | NM_198285.3(WDR86):c.280C>G (p.Arg94Gly) | not specified [RCV004142146] | uncertain significance | 7 | 151400125 | 151400125 | Human | | name |
| 155944336 | CV2295109 | single nucleotide variant | NM_198285.3(WDR86):c.209C>A (p.Ala70Asp) | not specified [RCV004156213] | uncertain significance | 7 | 151400196 | 151400196 | Human | | name |
| 156190663 | CV2301746 | single nucleotide variant | NM_198285.3(WDR86):c.224C>T (p.Ala75Val) | not specified [RCV004156560] | uncertain significance | 7 | 151400181 | 151400181 | Human | | name |
| 155931628 | CV2362603 | single nucleotide variant | NM_198285.3(WDR86):c.197A>T (p.Glu66Val) | not specified [RCV004215256] | uncertain significance | 7 | 151400208 | 151400208 | Human | | name |
| 405807529 | CV3356468 | single nucleotide variant | NM_198285.3(WDR86):c.182C>A (p.Thr61Asn) | not specified [RCV004480728] | uncertain significance | 7 | 151400223 | 151400223 | Human | | name |
| 407524294 | CV3489938 | single nucleotide variant | NM_198285.3(WDR86):c.106G>A (p.Asp36Asn) | not specified [RCV004678374] | uncertain significance | 7 | 151409484 | 151409484 | Human | | name |
| 407465339 | CV3489939 | single nucleotide variant | NM_198285.3(WDR86):c.176A>T (p.Tyr59Phe) | not specified [RCV004688744] | uncertain significance | 7 | 151400229 | 151400229 | Human | | name |
| 597791887 | CV3630014 | single nucleotide variant | NM_198285.3(WDR86):c.281G>A (p.Arg94Gln) | not specified [RCV004876808] | uncertain significance | 7 | 151400124 | 151400124 | Human | | name |
| 598266840 | CV3933447 | single nucleotide variant | NM_198285.3(WDR86):c.215C>T (p.Thr72Ile) | not specified [RCV005302040] | uncertain significance | 7 | 151400190 | 151400190 | Human | | name |
| 156168509 | CV2197693 | single nucleotide variant | NM_198285.3(WDR86):c.608C>T (p.Thr203Met) | not specified [RCV004074900] | uncertain significance | 7 | 151395894 | 151395894 | Human | | name |
| 155921367 | CV2240515 | single nucleotide variant | NM_198285.3(WDR86):c.416G>C (p.Cys139Ser) | not specified [RCV004119179] | uncertain significance | 7 | 151396086 | 151396086 | Human | | name |
| 156246006 | CV2263683 | single nucleotide variant | NM_198285.3(WDR86):c.712G>C (p.Val238Leu) | not specified [RCV004135980] | uncertain significance | 7 | 151395790 | 151395790 | Human | | name |
| 156142851 | CV2296144 | single nucleotide variant | NM_198285.3(WDR86):c.706G>A (p.Gly236Ser) | not specified [RCV004154072] | uncertain significance | 7 | 151395796 | 151395796 | Human | | name |
| 155930807 | CV2297080 | single nucleotide variant | NM_198285.3(WDR86):c.613G>T (p.Gly205Cys) | not specified [RCV004150990] | uncertain significance | 7 | 151395889 | 151395889 | Human | | name |
| 156035440 | CV2303453 | single nucleotide variant | NM_198285.3(WDR86):c.409C>T (p.Arg137Cys) | not specified [RCV004161568] | uncertain significance | 7 | 151396093 | 151396093 | Human | | name |
| 156172213 | CV2326768 | single nucleotide variant | NM_198285.3(WDR86):c.764G>C (p.Arg255Thr) | not specified [RCV004176611] | uncertain significance | 7 | 151385186 | 151385186 | Human | | name |
| 155982388 | CV2337156 | single nucleotide variant | NM_198285.3(WDR86):c.505G>A (p.Gly169Ser) | not specified [RCV004192915] | uncertain significance | 7 | 151395997 | 151395997 | Human | | name |
| 156086228 | CV2366269 | single nucleotide variant | NM_198285.3(WDR86):c.481G>A (p.Ala161Thr) | not specified [RCV004210285] | uncertain significance | 7 | 151396021 | 151396021 | Human | | name |
| 156286951 | CV2370440 | single nucleotide variant | NM_198285.3(WDR86):c.697G>A (p.Glu233Lys) | not specified [RCV004215791] | uncertain significance | 7 | 151395805 | 151395805 | Human | | name |
| 156389198 | CV2373632 | single nucleotide variant | NM_198285.3(WDR86):c.487G>A (p.Gly163Arg) | not specified [RCV004222722] | uncertain significance | 7 | 151396015 | 151396015 | Human | | name |
| 156082342 | CV2394736 | single nucleotide variant | NM_198285.3(WDR86):c.638C>T (p.Thr213Ile) | not specified [RCV004234412] | uncertain significance | 7 | 151395864 | 151395864 | Human | | name |
| 401780544 | CV2674073 | single nucleotide variant | NM_198285.3(WDR86):c.848A>G (p.Tyr283Cys) | not specified [RCV004295479] | uncertain significance | 7 | 151385102 | 151385102 | Human | | name |
| 401733725 | CV2682622 | single nucleotide variant | NM_198285.3(WDR86):c.805C>T (p.Arg269Cys) | not specified [RCV004292671] | uncertain significance | 7 | 151385145 | 151385145 | Human | | name |
| 401766016 | CV2717977 | single nucleotide variant | NM_198285.3(WDR86):c.568C>T (p.Arg190Trp) | not specified [RCV004321925] | uncertain significance | 7 | 151395934 | 151395934 | Human | | name |
| 405807531 | CV3356469 | single nucleotide variant | NM_198285.3(WDR86):c.350G>A (p.Arg117Gln) | not specified [RCV004480729] | uncertain significance | 7 | 151396152 | 151396152 | Human | | name |
| 405807533 | CV3356470 | single nucleotide variant | NM_198285.3(WDR86):c.652C>T (p.Arg218Cys) | not specified [RCV004480730] | uncertain significance | 7 | 151395850 | 151395850 | Human | | name |
| 405807535 | CV3356471 | single nucleotide variant | NM_198285.3(WDR86):c.671G>C (p.Ser224Thr) | not specified [RCV004480731] | uncertain significance | 7 | 151395831 | 151395831 | Human | | name |
| 405807537 | CV3356472 | single nucleotide variant | NM_198285.3(WDR86):c.703C>T (p.Arg235Trp) | not specified [RCV004480732] | uncertain significance | 7 | 151395799 | 151395799 | Human | | name |
| 405807539 | CV3356473 | single nucleotide variant | NM_198285.3(WDR86):c.737G>A (p.Arg246Gln) | not specified [RCV004480733] | uncertain significance | 7 | 151385213 | 151385213 | Human | | name |
| 405807541 | CV3356474 | single nucleotide variant | NM_198285.3(WDR86):c.769G>A (p.Val257Ile) | not specified [RCV004480734] | uncertain significance | 7 | 151385181 | 151385181 | Human | | name |
| 405807543 | CV3356475 | single nucleotide variant | NM_198285.3(WDR86):c.826C>T (p.Arg276Cys) | not specified [RCV004480735] | uncertain significance | 7 | 151385124 | 151385124 | Human | | name |
| 405807546 | CV3356476 | single nucleotide variant | NM_198285.3(WDR86):c.913G>A (p.Gly305Arg) | not specified [RCV004480736] | uncertain significance | 7 | 151381931 | 151381931 | Human | | name |
| 405807549 | CV3356478 | single nucleotide variant | NM_198285.3(WDR86):c.973G>A (p.Gly325Ser) | not specified [RCV004480738] | uncertain significance | 7 | 151381740 | 151381740 | Human | | name |
| 597791881 | CV3630010 | single nucleotide variant | NM_198285.3(WDR86):c.967G>A (p.Val323Met) | not specified [RCV004876806] | uncertain significance | 7 | 151381746 | 151381746 | Human | | name |
| 597739351 | CV3630011 | single nucleotide variant | NM_198285.3(WDR86):c.757G>A (p.Ala253Thr) | not specified [RCV004890331] | uncertain significance | 7 | 151385193 | 151385193 | Human | | name |
| 597791884 | CV3630012 | single nucleotide variant | NM_198285.3(WDR86):c.401G>A (p.Arg134Gln) | not specified [RCV004876807] | uncertain significance | 7 | 151396101 | 151396101 | Human | | name |
| 597739355 | CV3630013 | single nucleotide variant | NM_198285.3(WDR86):c.685C>T (p.Arg229Trp) | not specified [RCV004890332] | uncertain significance | 7 | 151395817 | 151395817 | Human | | name |
| 597791890 | CV3630015 | single nucleotide variant | NM_198285.3(WDR86):c.923G>C (p.Arg308Pro) | not specified [RCV004876809] | uncertain significance | 7 | 151381921 | 151381921 | Human | | name |
| 597739360 | CV3630016 | single nucleotide variant | NM_198285.3(WDR86):c.440C>T (p.Ala147Val) | not specified [RCV004890333] | uncertain significance | 7 | 151396062 | 151396062 | Human | | name |
| 597739477 | CV3630017 | single nucleotide variant | NM_198285.3(WDR86):c.387G>C (p.Met129Ile) | not specified [RCV004890334] | uncertain significance | 7 | 151396115 | 151396115 | Human | | name |
| 597791893 | CV3630018 | single nucleotide variant | NM_198285.3(WDR86):c.409C>A (p.Arg137Ser) | not specified [RCV004876810] | uncertain significance | 7 | 151396093 | 151396093 | Human | | name |
| 597739482 | CV3630019 | single nucleotide variant | NM_198285.3(WDR86):c.785C>T (p.Ala262Val) | not specified [RCV004890335] | uncertain significance | 7 | 151385165 | 151385165 | Human | | name |
| 597791896 | CV3630020 | single nucleotide variant | NM_198285.3(WDR86):c.979G>A (p.Val327Met) | not specified [RCV004876811] | uncertain significance | 7 | 151381734 | 151381734 | Human | | name |
| 598266827 | CV3933444 | single nucleotide variant | NM_198285.3(WDR86):c.613G>A (p.Gly205Ser) | not specified [RCV005302037] | likely benign | 7 | 151395889 | 151395889 | Human | | name |
| 598266832 | CV3933445 | single nucleotide variant | NM_198285.3(WDR86):c.815C>T (p.Thr272Met) | not specified [RCV005302038] | uncertain significance | 7 | 151385135 | 151385135 | Human | | name |
| 598266836 | CV3933446 | single nucleotide variant | NM_198285.3(WDR86):c.427C>G (p.Leu143Val) | not specified [RCV005302039] | uncertain significance | 7 | 151396075 | 151396075 | Human | | name |
| 156248736 | CV2203203 | single nucleotide variant | NM_198285.3(WDR86):c.1055C>G (p.Pro352Arg) | not specified [RCV004070898] | uncertain significance | 7 | 151381658 | 151381658 | Human | | name |
| 156276714 | CV2328078 | single nucleotide variant | NM_198285.3(WDR86):c.1034T>G (p.Leu345Arg) | not specified [RCV004173198] | uncertain significance | 7 | 151381679 | 151381679 | Human | | name |
| 156073423 | CV2331582 | single nucleotide variant | NM_198285.3(WDR86):c.1012C>T (p.Arg338Cys) | not specified [RCV004184223] | uncertain significance | 7 | 151381701 | 151381701 | Human | | name |
| 407524298 | CV3489940 | single nucleotide variant | NM_198285.3(WDR86):c.1055C>T (p.Pro352Leu) | not specified [RCV004678375] | uncertain significance | 7 | 151381658 | 151381658 | Human | | name |
