| 156189667 | CV2226855 | single nucleotide variant | NM_001367482.1(WDR64):c.23G>C (p.Arg8Pro) | not specified [RCV004103838] | uncertain significance | 1 | 241652507 | 241652507 | Human | | name |
| 156272426 | CV2323303 | single nucleotide variant | NM_001367482.1(WDR64):c.22C>T (p.Arg8Cys) | not specified [RCV004171717] | uncertain significance | 1 | 241652506 | 241652506 | Human | | name |
| 597791735 | CV3633772 | single nucleotide variant | NM_001367482.1(WDR64):c.14A>G (p.Lys5Arg) | not specified [RCV004876760] | uncertain significance | 1 | 241652498 | 241652498 | Human | | name |
| 156086137 | CV2390784 | single nucleotide variant | NM_001367482.1(WDR64):c.44T>A (p.Met15Lys) | not specified [RCV004241070] | uncertain significance | 1 | 241652528 | 241652528 | Human | | name |
| 329401606 | CV2457207 | single nucleotide variant | NM_001367482.1(WDR64):c.34G>A (p.Ala12Thr) | not specified [RCV004265283] | uncertain significance | 1 | 241652518 | 241652518 | Human | | name |
| 8624932 | CV80050 | single nucleotide variant | NM_144625.4(WDR64):c.1179G>A (p.Trp393Ter) | Malignant melanoma [RCV000060126] | not provided | 1 | 241738377 | 241738377 | Human | | name |
| 156324714 | CV2198847 | single nucleotide variant | NM_001367482.1(WDR64):c.236A>G (p.Lys79Arg) | not specified [RCV004077882] | uncertain significance | 1 | 241660620 | 241660620 | Human | | name |
| 156040151 | CV2219445 | single nucleotide variant | NM_001367482.1(WDR64):c.253G>A (p.Asp85Asn) | not specified [RCV004095229] | uncertain significance | 1 | 241660637 | 241660637 | Human | | name |
| 155903057 | CV2274811 | single nucleotide variant | NM_001367482.1(WDR64):c.223C>G (p.Arg75Gly) | not specified [RCV004139151] | uncertain significance | 1 | 241660607 | 241660607 | Human | | name |
| 155956374 | CV2304024 | single nucleotide variant | NM_001367482.1(WDR64):c.203T>G (p.Val68Gly) | not specified [RCV004170076] | uncertain significance | 1 | 241660587 | 241660587 | Human | | name |
| 156106861 | CV2355283 | single nucleotide variant | NM_001367482.1(WDR64):c.191T>C (p.Phe64Ser) | not specified [RCV004203134] | uncertain significance | 1 | 241660575 | 241660575 | Human | | name |
| 405807419 | CV3356348 | single nucleotide variant | NM_001367482.1(WDR64):c.224G>A (p.Arg75His) | not specified [RCV004480608] | uncertain significance | 1 | 241660608 | 241660608 | Human | | name |
| 407524103 | CV3489861 | single nucleotide variant | NM_001367482.1(WDR64):c.114T>G (p.Asp38Glu) | not specified [RCV004678300] | uncertain significance | 1 | 241652598 | 241652598 | Human | | name |
| 597739259 | CV3633778 | single nucleotide variant | NM_001367482.1(WDR64):c.215A>T (p.Asp72Val) | not specified [RCV004890311] | uncertain significance | 1 | 241660599 | 241660599 | Human | | name |
| 598266608 | CV3933340 | single nucleotide variant | NM_001367482.1(WDR64):c.251C>T (p.Thr84Met) | not specified [RCV005301981] | uncertain significance | 1 | 241660635 | 241660635 | Human | | name |
| 598266621 | CV3933343 | single nucleotide variant | NM_001367482.1(WDR64):c.227T>C (p.Phe76Ser) | not specified [RCV005301984] | uncertain significance | 1 | 241660611 | 241660611 | Human | | name |
| 155975216 | CV2235833 | single nucleotide variant | NM_001367482.1(WDR64):c.365G>A (p.Arg122Gln) | not specified [RCV004111949] | uncertain significance | 1 | 241671162 | 241671162 | Human | | name |
| 155958555 | CV2282217 | single nucleotide variant | NM_001367482.1(WDR64):c.880A>G (p.Arg294Gly) | not specified [RCV004132798] | uncertain significance | 1 | 241687501 | 241687501 | Human | | name |
| 155993202 | CV2286278 | single nucleotide variant | NM_001367482.1(WDR64):c.658T>G (p.Cys220Gly) | not specified [RCV004146231] | uncertain significance | 1 | 241683520 | 241683520 | Human | | name |
| 156254170 | CV2311517 | single nucleotide variant | NM_001367482.1(WDR64):c.638T>C (p.Val213Ala) | not specified [RCV004168346] | uncertain significance | 1 | 241683500 | 241683500 | Human | | name |
| 156161028 | CV2319430 | single nucleotide variant | NM_001367482.1(WDR64):c.586A>C (p.Ile196Leu) | not specified [RCV004185016] | uncertain significance | 1 | 241679557 | 241679557 | Human | | name |
| 155915092 | CV2339062 | single nucleotide variant | NM_001367482.1(WDR64):c.469G>C (p.Val157Leu) | not specified [RCV004187109] | uncertain significance | 1 | 241674733 | 241674733 | Human | | name |
| 156179248 | CV2374657 | single nucleotide variant | NM_001367482.1(WDR64):c.860A>G (p.Asn287Ser) | not specified [RCV004225274] | uncertain significance | 1 | 241687481 | 241687481 | Human | | name |
| 329378240 | CV2446906 | single nucleotide variant | NM_001367482.1(WDR64):c.682C>T (p.Pro228Ser) | not specified [RCV004257752] | likely benign | 1 | 241683544 | 241683544 | Human | | name |
| 401884976 | CV2766379 | single nucleotide variant | NM_001367482.1(WDR64):c.388A>G (p.Arg130Gly) | not specified [RCV004342625] | uncertain significance | 1 | 241674652 | 241674652 | Human | | name |
| 405807407 | CV3356354 | single nucleotide variant | NM_001367482.1(WDR64):c.598G>C (p.Asp200His) | not specified [RCV004480614] | uncertain significance | 1 | 241679569 | 241679569 | Human | | name |
| 405807405 | CV3356355 | single nucleotide variant | NM_001367482.1(WDR64):c.798A>C (p.Arg266Ser) | not specified [RCV004480615] | uncertain significance | 1 | 241683660 | 241683660 | Human | | name |
| 405807403 | CV3356356 | single nucleotide variant | NM_001367482.1(WDR64):c.827A>C (p.Lys276Thr) | not specified [RCV004480616] | uncertain significance | 1 | 241683689 | 241683689 | Human | | name |
| 405807401 | CV3356357 | single nucleotide variant | NM_001367482.1(WDR64):c.944T>G (p.Leu315Trp) | not specified [RCV004480617] | uncertain significance | 1 | 241687565 | 241687565 | Human | | name |
| 597791719 | CV3633763 | single nucleotide variant | NM_001367482.1(WDR64):c.917C>G (p.Ser306Cys) | not specified [RCV004876755] | uncertain significance | 1 | 241687538 | 241687538 | Human | | name |
| 597739233 | CV3633764 | single nucleotide variant | NM_001367482.1(WDR64):c.700T>G (p.Cys234Gly) | not specified [RCV004890305] | uncertain significance | 1 | 241683562 | 241683562 | Human | | name |
| 597739251 | CV3633774 | single nucleotide variant | NM_001367482.1(WDR64):c.878T>C (p.Ile293Thr) | not specified [RCV004890309] | uncertain significance | 1 | 241687499 | 241687499 | Human | | name |
| 598266642 | CV3933349 | single nucleotide variant | NM_001367482.1(WDR64):c.464T>C (p.Ile155Thr) | not specified [RCV005301989] | uncertain significance | 1 | 241674728 | 241674728 | Human | | name |
| 598266647 | CV3933350 | single nucleotide variant | NM_001367482.1(WDR64):c.649A>G (p.Met217Val) | not specified [RCV005301990] | uncertain significance | 1 | 241683511 | 241683511 | Human | | name |
| 598220076 | CV3933351 | single nucleotide variant | NM_001367482.1(WDR64):c.397G>A (p.Val133Met) | not specified [RCV005293426] | uncertain significance | 1 | 241674661 | 241674661 | Human | | name |
| 598266660 | CV3933354 | single nucleotide variant | NM_001367482.1(WDR64):c.431A>T (p.Asp144Val) | not specified [RCV005301993] | uncertain significance | 1 | 241674695 | 241674695 | Human | | name |
| 156358736 | CV2260773 | single nucleotide variant | NM_001367482.1(WDR64):c.2383C>T (p.Leu795Phe) | not specified [RCV004125691] | uncertain significance | 1 | 241772884 | 241772884 | Human | | name |
| 156014624 | CV2272188 | single nucleotide variant | NM_001367482.1(WDR64):c.2087G>A (p.Arg696Gln) | not specified [RCV004124958] | uncertain significance | 1 | 241769409 | 241769409 | Human | | name |
| 156092367 | CV2300133 | single nucleotide variant | NM_001367482.1(WDR64):c.1129T>C (p.Phe377Leu) | not specified [RCV004151323] | uncertain significance | 1 | 241723371 | 241723371 | Human | | name |
| 156204359 | CV2314135 | single nucleotide variant | NM_001367482.1(WDR64):c.2145T>G (p.Asn715Lys) | not specified [RCV004166222] | uncertain significance | 1 | 241769467 | 241769467 | Human | | name |
| 156068234 | CV2356818 | single nucleotide variant | NM_001367482.1(WDR64):c.1835A>C (p.Gln612Pro) | not specified [RCV004202158] | uncertain significance | 1 | 241757347 | 241757347 | Human | | name |
| 156136393 | CV2364934 | single nucleotide variant | NM_001367482.1(WDR64):c.1816G>C (p.Asp606His) | not specified [RCV004222230] | uncertain significance | 1 | 241757328 | 241757328 | Human | | name |
| 156083331 | CV2394944 | single nucleotide variant | NM_001367482.1(WDR64):c.2819T>C (p.Ile940Thr) | not specified [RCV004234593] | uncertain significance | 1 | 241787962 | 241787962 | Human | | name |
| 156088649 | CV2397478 | single nucleotide variant | NM_001367482.1(WDR64):c.2021C>G (p.Ala674Gly) | not specified [RCV004236953] | uncertain significance | 1 | 241766291 | 241766291 | Human | | name |
| 329361109 | CV2436678 | single nucleotide variant | NM_001367482.1(WDR64):c.1421A>G (p.Asn474Ser) | not specified [RCV004258050] | uncertain significance | 1 | 241741615 | 241741615 | Human | | name |
| 329390996 | CV2447602 | single nucleotide variant | NM_001367482.1(WDR64):c.1190C>A (p.Ala397Glu) | not specified [RCV004258407] | uncertain significance | 1 | 241723432 | 241723432 | Human | | name |
| 329355225 | CV2449290 | single nucleotide variant | NM_001367482.1(WDR64):c.1397G>A (p.Arg466Gln) | not specified [RCV004257421] | uncertain significance | 1 | 241741591 | 241741591 | Human | | name |
| 329379086 | CV2460147 | single nucleotide variant | NM_001367482.1(WDR64):c.1222C>T (p.Leu408Phe) | not specified [RCV004273252] | uncertain significance | 1 | 241738390 | 241738390 | Human | | name |
| 329362895 | CV2464823 | single nucleotide variant | NM_001367482.1(WDR64):c.1489G>A (p.Gly497Arg) | not specified [RCV004284772] | uncertain significance | 1 | 241744411 | 241744411 | Human | | name |
| 329387411 | CV2470665 | single nucleotide variant | NM_001367482.1(WDR64):c.1319C>A (p.Thr440Lys) | not specified [RCV004273919] | uncertain significance | 1 | 241738487 | 241738487 | Human | | name |
| 401718062 | CV2689598 | single nucleotide variant | NM_001367482.1(WDR64):c.2662G>C (p.Glu888Gln) | not specified [RCV004309018] | uncertain significance | 1 | 241783338 | 241783338 | Human | | name |
| 401728845 | CV2693868 | single nucleotide variant | NM_001367482.1(WDR64):c.1073G>A (p.Arg358Gln) | not specified [RCV004300171] | uncertain significance | 1 | 241723315 | 241723315 | Human | | name |
| 401759168 | CV2705415 | single nucleotide variant | NM_001367482.1(WDR64):c.2191A>T (p.Ser731Cys) | not specified [RCV004312081] | uncertain significance | 1 | 241770628 | 241770628 | Human | | name |
| 401750795 | CV2715765 | single nucleotide variant | NM_001367482.1(WDR64):c.2648T>C (p.Val883Ala) | not specified [RCV004328902] | uncertain significance | 1 | 241783324 | 241783324 | Human | | name |
| 401762389 | CV2723422 | single nucleotide variant | NM_001367482.1(WDR64):c.1823T>A (p.Val608Glu) | not specified [RCV004323497] | uncertain significance | 1 | 241757335 | 241757335 | Human | | name |
| 401871978 | CV2754246 | single nucleotide variant | NM_001367482.1(WDR64):c.1040T>C (p.Val347Ala) | not specified [RCV004334432] | uncertain significance | 1 | 241711867 | 241711867 | Human | | name |
| 401876864 | CV2754525 | single nucleotide variant | NM_001367482.1(WDR64):c.2018C>T (p.Ala673Val) | not provided [RCV004691580]|not specified [RCV004336731] | uncertain significance | 1 | 241766288 | 241766288 | Human | | name |
| 401893611 | CV2765370 | single nucleotide variant | NM_001367482.1(WDR64):c.2353G>C (p.Ala785Pro) | not specified [RCV004339873] | uncertain significance | 1 | 241772854 | 241772854 | Human | | name |
| 401887625 | CV2772055 | single nucleotide variant | NM_001367482.1(WDR64):c.1106T>C (p.Val369Ala) | not specified [RCV004344725] | uncertain significance | 1 | 241723348 | 241723348 | Human | | name |
| 405807431 | CV3356342 | single nucleotide variant | NM_001367482.1(WDR64):c.1051G>A (p.Gly351Arg) | not specified [RCV004480602] | uncertain significance | 1 | 241711878 | 241711878 | Human | | name |
| 405807427 | CV3356344 | single nucleotide variant | NM_001367482.1(WDR64):c.1379T>C (p.Val460Ala) | not specified [RCV004480604] | uncertain significance | 1 | 241741573 | 241741573 | Human | | name |
| 405807423 | CV3356346 | single nucleotide variant | NM_001367482.1(WDR64):c.2171C>G (p.Pro724Arg) | not specified [RCV004480606] | uncertain significance | 1 | 241769493 | 241769493 | Human | | name |
| 405807421 | CV3356347 | single nucleotide variant | NM_001367482.1(WDR64):c.2246G>A (p.Ser749Asn) | not specified [RCV004480607] | uncertain significance | 1 | 241770683 | 241770683 | Human | | name |
| 405807417 | CV3356349 | single nucleotide variant | NM_001367482.1(WDR64):c.2620C>T (p.Arg874Cys) | not specified [RCV004480609] | uncertain significance | 1 | 241783296 | 241783296 | Human | | name |
| 405807415 | CV3356350 | single nucleotide variant | NM_001367482.1(WDR64):c.2716G>A (p.Ala906Thr) | not specified [RCV004480610] | uncertain significance | 1 | 241787859 | 241787859 | Human | | name |
| 405807413 | CV3356351 | single nucleotide variant | NM_001367482.1(WDR64):c.2777C>G (p.Thr926Arg) | not specified [RCV004480611] | uncertain significance | 1 | 241787920 | 241787920 | Human | | name |
| 405807411 | CV3356352 | single nucleotide variant | NM_001367482.1(WDR64):c.2865A>C (p.Glu955Asp) | not specified [RCV004480612] | uncertain significance | 1 | 241788008 | 241788008 | Human | | name |
| 407465320 | CV3489855 | single nucleotide variant | NM_001367482.1(WDR64):c.1420A>G (p.Asn474Asp) | not specified [RCV004688739] | uncertain significance | 1 | 241741614 | 241741614 | Human | | name |
| 407524090 | CV3489856 | single nucleotide variant | NM_001367482.1(WDR64):c.1378G>T (p.Val460Phe) | not specified [RCV004678296] | uncertain significance | 1 | 241741572 | 241741572 | Human | | name |
| 407524093 | CV3489857 | single nucleotide variant | NM_001367482.1(WDR64):c.2396A>C (p.His799Pro) | not specified [RCV004678297] | uncertain significance | 1 | 241772897 | 241772897 | Human | | name |
| 407465324 | CV3489859 | single nucleotide variant | NM_001367482.1(WDR64):c.1342T>C (p.Tyr448His) | not specified [RCV004688740] | uncertain significance | 1 | 241741536 | 241741536 | Human | | name |
| 407524106 | CV3489862 | single nucleotide variant | NM_001367482.1(WDR64):c.2369C>T (p.Ala790Val) | not specified [RCV004678301] | uncertain significance | 1 | 241772870 | 241772870 | Human | | name |
| 597791718 | CV3633760 | single nucleotide variant | NM_001367482.1(WDR64):c.2900A>G (p.Lys967Arg) | not specified [RCV004876754] | uncertain significance | 1 | 241790599 | 241790599 | Human | | name |
| 597739224 | CV3633761 | single nucleotide variant | NM_001367482.1(WDR64):c.2094A>C (p.Glu698Asp) | not specified [RCV004890303] | uncertain significance | 1 | 241769416 | 241769416 | Human | | name |
| 597739238 | CV3633765 | single nucleotide variant | NM_001367482.1(WDR64):c.1589A>G (p.Tyr530Cys) | not specified [RCV004890306] | uncertain significance | 1 | 241744511 | 241744511 | Human | | name |
| 597791722 | CV3633766 | single nucleotide variant | NM_001367482.1(WDR64):c.2565C>G (p.Ser855Arg) | not specified [RCV004876756] | uncertain significance | 1 | 241780032 | 241780032 | Human | | name |
| 597739241 | CV3633767 | single nucleotide variant | NM_001367482.1(WDR64):c.2436A>T (p.Arg812Ser) | not specified [RCV004890307] | uncertain significance | 1 | 241775110 | 241775110 | Human | | name |
| 597791726 | CV3633768 | single nucleotide variant | NM_001367482.1(WDR64):c.1586C>T (p.Ala529Val) | not specified [RCV004876757] | uncertain significance | 1 | 241744508 | 241744508 | Human | | name |
| 597791729 | CV3633769 | single nucleotide variant | NM_001367482.1(WDR64):c.2620C>A (p.Arg874Ser) | not specified [RCV004876758] | uncertain significance | 1 | 241783296 | 241783296 | Human | | name |
| 597739246 | CV3633770 | single nucleotide variant | NM_001367482.1(WDR64):c.2953G>A (p.Val985Met) | not specified [RCV004890308] | uncertain significance | 1 | 241790652 | 241790652 | Human | | name |
| 597791732 | CV3633771 | single nucleotide variant | NM_001367482.1(WDR64):c.2003G>T (p.Gly668Val) | not specified [RCV004876759] | uncertain significance | 1 | 241766273 | 241766273 | Human | | name |
| 597791738 | CV3633773 | single nucleotide variant | NM_001367482.1(WDR64):c.2414G>A (p.Arg805His) | not specified [RCV004876761] | uncertain significance | 1 | 241772915 | 241772915 | Human | | name |
| 597791741 | CV3633775 | single nucleotide variant | NM_001367482.1(WDR64):c.2984T>C (p.Leu995Pro) | not specified [RCV004876762] | uncertain significance | 1 | 241790683 | 241790683 | Human | | name |
| 597739254 | CV3633776 | single nucleotide variant | NM_001367482.1(WDR64):c.1322G>C (p.Gly441Ala) | not specified [RCV004890310] | uncertain significance | 1 | 241741516 | 241741516 | Human | | name |
| 598266603 | CV3933339 | single nucleotide variant | NM_001367482.1(WDR64):c.2753G>A (p.Arg918Gln) | not specified [RCV005301980] | uncertain significance | 1 | 241787896 | 241787896 | Human | | name |
| 598266616 | CV3933342 | single nucleotide variant | NM_001367482.1(WDR64):c.1808A>T (p.Glu603Val) | not specified [RCV005301983] | uncertain significance | 1 | 241757320 | 241757320 | Human | | name |
| 598266625 | CV3933344 | single nucleotide variant | NM_001367482.1(WDR64):c.2203A>G (p.Ile735Val) | not specified [RCV005301985] | likely benign | 1 | 241770640 | 241770640 | Human | | name |
| 598220071 | CV3933346 | single nucleotide variant | NM_001367482.1(WDR64):c.2708T>G (p.Leu903Arg) | not specified [RCV005293425] | uncertain significance | 1 | 241787851 | 241787851 | Human | | name |
| 598266634 | CV3933347 | single nucleotide variant | NM_001367482.1(WDR64):c.2483T>C (p.Leu828Pro) | not specified [RCV005301987] | uncertain significance | 1 | 241775157 | 241775157 | Human | | name |
| 598266655 | CV3933353 | single nucleotide variant | NM_001367482.1(WDR64):c.2473G>C (p.Ala825Pro) | not specified [RCV005301992] | uncertain significance | 1 | 241775147 | 241775147 | Human | | name |
| 598220081 | CV3933355 | single nucleotide variant | NM_001367482.1(WDR64):c.1712A>G (p.Glu571Gly) | not specified [RCV005293427] | uncertain significance | 1 | 241749664 | 241749664 | Human | | name |
| 405807409 | CV3356353 | single nucleotide variant | NM_001367482.1(WDR64):c.3002G>C (p.Arg1001Pro) | not specified [RCV004480613] | uncertain significance | 1 | 241795211 | 241795211 | Human | | name |
| 407524096 | CV3489858 | single nucleotide variant | NM_001367482.1(WDR64):c.3182A>G (p.Gln1061Arg) | not specified [RCV004678298] | uncertain significance | 1 | 241796360 | 241796360 | Human | | name |
| 407524108 | CV3489863 | single nucleotide variant | NM_001367482.1(WDR64):c.3056T>C (p.Phe1019Ser) | not specified [RCV004678302] | uncertain significance | 1 | 241795265 | 241795265 | Human | | name |
| 597739228 | CV3633762 | single nucleotide variant | NM_001367482.1(WDR64):c.3025G>A (p.Val1009Met) | not specified [RCV004890304] | likely benign | 1 | 241795234 | 241795234 | Human | | name |
| 597791744 | CV3633777 | single nucleotide variant | NM_001367482.1(WDR64):c.3268C>T (p.Pro1090Ser) | not specified [RCV004876763] | uncertain significance | 1 | 241801207 | 241801207 | Human | | name |
| 598266612 | CV3933341 | single nucleotide variant | NM_001367482.1(WDR64):c.3116T>C (p.Ile1039Thr) | not specified [RCV005301982] | uncertain significance | 1 | 241796294 | 241796294 | Human | | name |
| 598266629 | CV3933345 | single nucleotide variant | NM_001367482.1(WDR64):c.3230C>T (p.Pro1077Leu) | not specified [RCV005301986] | uncertain significance | 1 | 241801169 | 241801169 | Human | | name |
| 598266651 | CV3933352 | single nucleotide variant | NM_001367482.1(WDR64):c.3173G>C (p.Gly1058Ala) | not specified [RCV005301991] | uncertain significance | 1 | 241796351 | 241796351 | Human | | name |
