| 598233658 | CV3995055 | single nucleotide variant | NM_006600.4(NUDC):c.26G>C (p.Arg9Pro) | not specified [RCV005381753] | uncertain significance | 1 | 26921874 | 26921874 | Human | | name |
| 156182965 | CV2338241 | single nucleotide variant | NM_006600.4(NUDC):c.82C>G (p.Leu28Val) | not specified [RCV004186302] | uncertain significance | 1 | 26924089 | 26924089 | Human | | name |
| 408367670 | CV3511480 | single nucleotide variant | NM_006600.4(NUDC):c.606C>T (p.Ile202=) | NUDC-related condition [RCV004759078] | likely benign | 1 | 26942930 | 26942930 | Human | | name , trait |
| 597709525 | CV3573511 | single nucleotide variant | NM_006600.4(NUDC):c.37A>G (p.Met13Val) | not specified [RCV004840684] | uncertain significance | 1 | 26921885 | 26921885 | Human | | name |
| 156052965 | CV2320345 | single nucleotide variant | NM_006600.4(NUDC):c.242G>A (p.Arg81Gln) | not specified [RCV004178507] | uncertain significance | 1 | 26941539 | 26941539 | Human | | name |
| 156165509 | CV2330053 | single nucleotide variant | NM_006600.4(NUDC):c.281A>C (p.Glu94Ala) | not specified [RCV004185545] | uncertain significance | 1 | 26941578 | 26941578 | Human | | name |
| 329362939 | CV2464851 | single nucleotide variant | NM_006600.4(NUDC):c.265G>T (p.Ala89Ser) | not specified [RCV004284796] | uncertain significance | 1 | 26941562 | 26941562 | Human | | name |
| 401730699 | CV2686660 | single nucleotide variant | NM_006600.4(NUDC):c.244C>T (p.Arg82Trp) | not specified [RCV004300072] | uncertain significance | 1 | 26941541 | 26941541 | Human | | name |
| 405728912 | CV3355830 | single nucleotide variant | NM_006600.4(NUDC):c.209G>A (p.Arg70Gln) | not specified [RCV004496126] | uncertain significance | 1 | 26941506 | 26941506 | Human | | name |
| 407521698 | CV3462265 | single nucleotide variant | NM_006600.4(NUDC):c.238G>A (p.Glu80Lys) | not specified [RCV004652615] | uncertain significance | 1 | 26941535 | 26941535 | Human | | name |
| 407477495 | CV3462266 | single nucleotide variant | NM_006600.4(NUDC):c.254C>T (p.Ala85Val) | not specified [RCV004638823] | uncertain significance | 1 | 26941551 | 26941551 | Human | | name |
| 597709514 | CV3573510 | single nucleotide variant | NM_006600.4(NUDC):c.245G>A (p.Arg82Gln) | not specified [RCV004840683] | uncertain significance | 1 | 26941542 | 26941542 | Human | | name |
| 598233674 | CV3995058 | single nucleotide variant | NM_006600.4(NUDC):c.140A>G (p.Glu47Gly) | not specified [RCV005381755] | uncertain significance | 1 | 26924147 | 26924147 | Human | | name |
| 155993916 | CV2286350 | single nucleotide variant | NM_006600.4(NUDC):c.776C>T (p.Ser259Phe) | not specified [RCV004139881] | uncertain significance | 1 | 26945424 | 26945424 | Human | | name |
| 329393224 | CV2449575 | single nucleotide variant | NM_006600.4(NUDC):c.502G>T (p.Asp168Tyr) | not specified [RCV004268502] | uncertain significance | 1 | 26942732 | 26942732 | Human | | name |
| 401864246 | CV2767570 | single nucleotide variant | NM_006600.4(NUDC):c.557C>T (p.Pro186Leu) | not specified [RCV004343720] | uncertain significance | 1 | 26942881 | 26942881 | Human | | name |
| 401864249 | CV2767571 | single nucleotide variant | NM_006600.4(NUDC):c.563G>T (p.Cys188Phe) | not specified [RCV004343721] | uncertain significance | 1 | 26942887 | 26942887 | Human | | name |
| 401885852 | CV2783411 | single nucleotide variant | NM_006600.4(NUDC):c.469G>A (p.Gly157Arg) | not specified [RCV004365762] | uncertain significance | 1 | 26942699 | 26942699 | Human | | name |
| 401871937 | CV2783639 | single nucleotide variant | NM_006600.4(NUDC):c.647C>T (p.Ala216Val) | not specified [RCV004360286] | uncertain significance | 1 | 26942971 | 26942971 | Human | | name |
| 405728920 | CV3355831 | single nucleotide variant | NM_006600.4(NUDC):c.299C>T (p.Ser100Leu) | not specified [RCV004496127] | uncertain significance | 1 | 26941596 | 26941596 | Human | | name |
| 405728928 | CV3355832 | single nucleotide variant | NM_006600.4(NUDC):c.767G>A (p.Arg256His) | not specified [RCV004496128] | uncertain significance | 1 | 26945415 | 26945415 | Human | | name |
| 405728935 | CV3355833 | single nucleotide variant | NM_006600.4(NUDC):c.884G>A (p.Arg295Gln) | not specified [RCV004496129] | uncertain significance | 1 | 26945626 | 26945626 | Human | | name |
| 405728948 | CV3355834 | single nucleotide variant | NM_006600.4(NUDC):c.895A>G (p.Met299Val) | not specified [RCV004496130] | uncertain significance | 1 | 26945637 | 26945637 | Human | | name |
| 405728956 | CV3355835 | single nucleotide variant | NM_006600.4(NUDC):c.962C>T (p.Pro321Leu) | not specified [RCV004496131] | uncertain significance | 1 | 26946147 | 26946147 | Human | | name |
| 407521694 | CV3462263 | single nucleotide variant | NM_006600.4(NUDC):c.622C>T (p.Arg208Trp) | not specified [RCV004652614] | uncertain significance | 1 | 26942946 | 26942946 | Human | | name |
| 407477488 | CV3462264 | single nucleotide variant | NM_006600.4(NUDC):c.403G>A (p.Gly135Ser) | not specified [RCV004638822] | uncertain significance | 1 | 26941792 | 26941792 | Human | | name |
| 407521702 | CV3462267 | single nucleotide variant | NM_006600.4(NUDC):c.746A>G (p.Asn249Ser) | not specified [RCV004652616] | uncertain significance | 1 | 26945394 | 26945394 | Human | | name |
| 407477501 | CV3462268 | single nucleotide variant | NM_006600.4(NUDC):c.449A>C (p.Glu150Ala) | not specified [RCV004638824] | uncertain significance | 1 | 26942679 | 26942679 | Human | | name |
| 598265557 | CV3995053 | single nucleotide variant | NM_006600.4(NUDC):c.416C>T (p.Ser139Phe) | not specified [RCV005387967] | uncertain significance | 1 | 26941805 | 26941805 | Human | | name |
| 598233649 | CV3995054 | single nucleotide variant | NM_006600.4(NUDC):c.766C>T (p.Arg256Cys) | not specified [RCV005381752] | uncertain significance | 1 | 26945414 | 26945414 | Human | | name |
| 598233665 | CV3995056 | single nucleotide variant | NM_006600.4(NUDC):c.915C>A (p.Asp305Glu) | not specified [RCV005381754] | uncertain significance | 1 | 26945657 | 26945657 | Human | | name |
| 598265562 | CV3995057 | single nucleotide variant | NM_006600.4(NUDC):c.610C>T (p.Arg204Trp) | not specified [RCV005387968] | uncertain significance | 1 | 26942934 | 26942934 | Human | | name |
| 8590832 | CV125541 | single nucleotide variant | NM_015332.3(NUDCD3):c.976-128G>A | Lung cancer [RCV000106060] | uncertain significance | 7 | 44386249 | 44386249 | Human | | name |
| 8590833 | CV125542 | single nucleotide variant | NM_015332.3(NUDCD3):c.193-837C>T | Lung cancer [RCV000106061] | uncertain significance | 7 | 44486121 | 44486121 | Human | | name |
| 405729070 | CV3355848 | single nucleotide variant | NM_015332.4(NUDCD3):c.13G>T (p.Ala5Ser) | not specified [RCV004496144] | uncertain significance | 7 | 44490588 | 44490588 | Human | | name |
| 407477508 | CV3462278 | single nucleotide variant | NM_015332.4(NUDCD3):c.17C>T (p.Ala6Val) | not specified [RCV004638825] | uncertain significance | 7 | 44490584 | 44490584 | Human | | name |
| 156402461 | CV2361456 | single nucleotide variant | NM_145266.6(NUDCD2):c.29G>A (p.Gly10Glu) | not specified [RCV004221097] | uncertain significance | 5 | 163460022 | 163460022 | Human | | name |
| 155937568 | CV2380040 | single nucleotide variant | NM_032869.4(NUDCD1):c.91C>G (p.Pro31Ala) | not specified [RCV004222174] | uncertain significance | 8 | 109333920 | 109333920 | Human | | name |
| 329386261 | CV2454920 | single nucleotide variant | NM_032869.4(NUDCD1):c.36G>T (p.Lys12Asn) | not specified [RCV004270412] | uncertain significance | 8 | 109333975 | 109333975 | Human | | name |
| 401784115 | CV2721057 | single nucleotide variant | NM_145266.6(NUDCD2):c.31G>A (p.Val11Met) | not specified [RCV004328324] | uncertain significance | 5 | 163460020 | 163460020 | Human | | name |
| 407521705 | CV3462269 | single nucleotide variant | NM_032869.4(NUDCD1):c.56G>A (p.Arg19His) | not specified [RCV004652617] | uncertain significance | 8 | 109333955 | 109333955 | Human | | name |
| 407521710 | CV3462270 | single nucleotide variant | NM_032869.4(NUDCD1):c.61G>A (p.Glu21Lys) | not specified [RCV004652618] | uncertain significance | 8 | 109333950 | 109333950 | Human | | name |
| 597709542 | CV3573514 | single nucleotide variant | NM_145266.6(NUDCD2):c.97C>A (p.Gln33Lys) | not specified [RCV004840686] | uncertain significance | 5 | 163459954 | 163459954 | Human | | name |
| 598233721 | CV3995067 | single nucleotide variant | NM_145266.6(NUDCD2):c.41G>T (p.Cys14Phe) | not specified [RCV005381761] | uncertain significance | 5 | 163460010 | 163460010 | Human | | name |
| 156373939 | CV2198096 | single nucleotide variant | NM_015332.4(NUDCD3):c.122A>G (p.Tyr41Cys) | not specified [RCV004079695] | uncertain significance | 7 | 44490479 | 44490479 | Human | | name |
| 156284836 | CV2317578 | single nucleotide variant | NM_032869.4(NUDCD1):c.230A>G (p.Tyr77Cys) | not specified [RCV004172529] | uncertain significance | 8 | 109322352 | 109322352 | Human | | name |
| 156088961 | CV2392015 | single nucleotide variant | NM_015332.4(NUDCD3):c.280G>A (p.Glu94Lys) | not specified [RCV004235871] | uncertain significance | 7 | 44485197 | 44485197 | Human | | name |
| 155996949 | CV2398630 | single nucleotide variant | NM_145266.6(NUDCD2):c.252G>A (p.Met84Ile) | not specified [RCV004603429] | uncertain significance | 5 | 163457067 | 163457067 | Human | | name |
| 329366037 | CV2438027 | single nucleotide variant | NM_015332.4(NUDCD3):c.134G>A (p.Arg45His) | not specified [RCV004263733] | uncertain significance | 7 | 44490467 | 44490467 | Human | | name |
| 401780419 | CV2674016 | single nucleotide variant | NM_145266.6(NUDCD2):c.149G>A (p.Arg50Gln) | not specified [RCV004293381] | uncertain significance | 5 | 163459902 | 163459902 | Human | | name |
| 401879575 | CV2769670 | single nucleotide variant | NM_032869.4(NUDCD1):c.155C>T (p.Thr52Ile) | not specified [RCV004351597] | uncertain significance | 8 | 109322427 | 109322427 | Human | | name |
| 405729032 | CV3355844 | single nucleotide variant | NM_145266.6(NUDCD2):c.139C>T (p.Leu47Phe) | not specified [RCV004496140] | uncertain significance | 5 | 163459912 | 163459912 | Human | | name |
| 405729048 | CV3355845 | single nucleotide variant | NM_145266.6(NUDCD2):c.148C>G (p.Arg50Gly) | not specified [RCV004496141] | uncertain significance | 5 | 163459903 | 163459903 | Human | | name |
| 405729053 | CV3355846 | single nucleotide variant | NM_145266.6(NUDCD2):c.184C>T (p.Leu62Phe) | not specified [RCV004496142] | uncertain significance | 5 | 163459867 | 163459867 | Human | | name |
| 407521722 | CV3462274 | single nucleotide variant | NM_145266.6(NUDCD2):c.107C>T (p.Pro36Leu) | not specified [RCV004652622] | uncertain significance | 5 | 163459944 | 163459944 | Human | | name |
| 407521725 | CV3462275 | single nucleotide variant | NM_015332.4(NUDCD3):c.277G>A (p.Glu93Lys) | not specified [RCV004652623] | uncertain significance | 7 | 44485200 | 44485200 | Human | | name |
| 597643624 | CV3573515 | single nucleotide variant | NM_015332.4(NUDCD3):c.220C>T (p.Arg74Cys) | not specified [RCV004832638] | uncertain significance | 7 | 44485257 | 44485257 | Human | | name |
| 598233682 | CV3995059 | single nucleotide variant | NM_032869.4(NUDCD1):c.226T>C (p.Tyr76His) | not specified [RCV005381756] | uncertain significance | 8 | 109322356 | 109322356 | Human | | name |
| 598265582 | CV3995066 | single nucleotide variant | NM_145266.6(NUDCD2):c.196C>G (p.Leu66Val) | not specified [RCV005387971] | uncertain significance | 5 | 163457604 | 163457604 | Human | | name |
| 156083160 | CV2205496 | single nucleotide variant | NM_015332.4(NUDCD3):c.402G>C (p.Gln134His) | not specified [RCV004082431] | uncertain significance | 7 | 44485075 | 44485075 | Human | | name |
| 156044374 | CV2237657 | single nucleotide variant | NM_032869.4(NUDCD1):c.916T>A (p.Phe306Ile) | not specified [RCV004106583] | uncertain significance | 8 | 109281080 | 109281080 | Human | | name |
| 156055001 | CV2269616 | single nucleotide variant | NM_032869.4(NUDCD1):c.938T>C (p.Ile313Thr) | not specified [RCV004124710] | uncertain significance | 8 | 109281058 | 109281058 | Human | | name |
| 155980956 | CV2272790 | single nucleotide variant | NM_032869.4(NUDCD1):c.536C>T (p.Ser179Phe) | not specified [RCV004135703] | uncertain significance | 8 | 109293448 | 109293448 | Human | | name |
| 155931065 | CV2297211 | single nucleotide variant | NM_015332.4(NUDCD3):c.880A>G (p.Met294Val) | not specified [RCV004151098] | uncertain significance | 7 | 44392392 | 44392392 | Human | | name |
| 155912697 | CV2308957 | single nucleotide variant | NM_032869.4(NUDCD1):c.992A>G (p.His331Arg) | not specified [RCV004169241] | uncertain significance | 8 | 109281004 | 109281004 | Human | | name |
| 156252649 | CV2311389 | single nucleotide variant | NM_015332.4(NUDCD3):c.704G>A (p.Arg235His) | not specified [RCV004166449] | uncertain significance | 7 | 44404522 | 44404522 | Human | | name |
| 156355542 | CV2324506 | single nucleotide variant | NM_015332.4(NUDCD3):c.910G>A (p.Val304Met) | not specified [RCV004178987] | uncertain significance | 7 | 44392362 | 44392362 | Human | | name |
| 156199314 | CV2331283 | single nucleotide variant | NM_015332.4(NUDCD3):c.706G>A (p.Val236Ile) | not specified [RCV004181883] | uncertain significance | 7 | 44404520 | 44404520 | Human | | name |
| 156286271 | CV2345652 | single nucleotide variant | NM_015332.4(NUDCD3):c.959C>T (p.Pro320Leu) | not specified [RCV004205596] | uncertain significance | 7 | 44392313 | 44392313 | Human | | name |
| 156196666 | CV2367255 | single nucleotide variant | NM_032869.4(NUDCD1):c.353C>T (p.Ser118Phe) | not specified [RCV004215676] | uncertain significance | 8 | 109296490 | 109296490 | Human | | name |
| 156017071 | CV2370036 | single nucleotide variant | NM_032869.4(NUDCD1):c.668G>A (p.Arg223His) | not specified [RCV004210933] | uncertain significance | 8 | 109289906 | 109289906 | Human | | name |
| 155906892 | CV2379158 | single nucleotide variant | NM_032869.4(NUDCD1):c.726T>A (p.Asn242Lys) | not specified [RCV004235948] | uncertain significance | 8 | 109289848 | 109289848 | Human | | name |
| 155991372 | CV2384224 | single nucleotide variant | NM_145266.6(NUDCD2):c.310C>G (p.Leu104Val) | not specified [RCV004227618] | uncertain significance | 5 | 163457009 | 163457009 | Human | | name |
| 156049849 | CV2391122 | single nucleotide variant | NM_032869.4(NUDCD1):c.580A>G (p.Met194Val) | not specified [RCV004235102] | uncertain significance | 8 | 109293404 | 109293404 | Human | | name |
| 329400795 | CV2448904 | single nucleotide variant | NM_015332.4(NUDCD3):c.781G>A (p.Val261Ile) | not specified [RCV004261943] | uncertain significance | 7 | 44404445 | 44404445 | Human | | name |
| 329352419 | CV2452997 | single nucleotide variant | NM_032869.4(NUDCD1):c.619A>C (p.Thr207Pro) | not specified [RCV004277621] | uncertain significance | 8 | 109293365 | 109293365 | Human | | name |
| 329394932 | CV2457739 | single nucleotide variant | NM_032869.4(NUDCD1):c.510C>G (p.Ile170Met) | not specified [RCV004269575] | uncertain significance | 8 | 109293474 | 109293474 | Human | | name |
| 329389263 | CV2467227 | single nucleotide variant | NM_032869.4(NUDCD1):c.407T>C (p.Leu136Ser) | not specified [RCV004285039] | uncertain significance | 8 | 109296436 | 109296436 | Human | | name |
| 401718957 | CV2704885 | single nucleotide variant | NM_145266.6(NUDCD2):c.467A>C (p.Glu156Ala) | not specified [RCV004307462] | uncertain significance | 5 | 163453974 | 163453974 | Human | | name |
| 401734007 | CV2713294 | single nucleotide variant | NM_032869.4(NUDCD1):c.392A>C (p.Asp131Ala) | not specified [RCV004316814] | uncertain significance | 8 | 109296451 | 109296451 | Human | | name |
| 401783662 | CV2723816 | single nucleotide variant | NM_032869.4(NUDCD1):c.673A>G (p.Ile225Val) | not specified [RCV004325964] | likely benign | 8 | 109289901 | 109289901 | Human | | name |
| 401880451 | CV2763045 | single nucleotide variant | NM_032869.4(NUDCD1):c.679C>T (p.Arg227Cys) | not specified [RCV004336103] | likely benign | 8 | 109289895 | 109289895 | Human | | name |
| 401878698 | CV2776967 | single nucleotide variant | NM_032869.4(NUDCD1):c.724A>G (p.Asn242Asp) | not specified [RCV004351777] | uncertain significance | 8 | 109289850 | 109289850 | Human | | name |
| 405729001 | CV3355840 | single nucleotide variant | NM_032869.4(NUDCD1):c.827C>T (p.Pro276Leu) | not specified [RCV004496136] | uncertain significance | 8 | 109281169 | 109281169 | Human | | name |
| 405729009 | CV3355841 | single nucleotide variant | NM_032869.4(NUDCD1):c.856G>T (p.Asp286Tyr) | not specified [RCV004496137] | uncertain significance | 8 | 109281140 | 109281140 | Human | | name |
| 405729015 | CV3355842 | single nucleotide variant | NM_032869.4(NUDCD1):c.980C>T (p.Ser327Leu) | not specified [RCV004496138] | uncertain significance | 8 | 109281016 | 109281016 | Human | | name |
| 405729022 | CV3355843 | single nucleotide variant | NM_032869.4(NUDCD1):c.983C>T (p.Ser328Phe) | not specified [RCV004496139] | uncertain significance | 8 | 109281013 | 109281013 | Human | | name |
| 405729064 | CV3355847 | single nucleotide variant | NM_145266.6(NUDCD2):c.436A>G (p.Thr146Ala) | not specified [RCV004496143] | uncertain significance | 5 | 163454005 | 163454005 | Human | | name |
| 405729080 | CV3355849 | single nucleotide variant | NM_015332.4(NUDCD3):c.307G>A (p.Ala103Thr) | not specified [RCV004496145] | uncertain significance | 7 | 44485170 | 44485170 | Human | | name |
| 405729087 | CV3355850 | single nucleotide variant | NM_015332.4(NUDCD3):c.338T>G (p.Val113Gly) | not specified [RCV004496146] | uncertain significance | 7 | 44485139 | 44485139 | Human | | name |
| 407521716 | CV3462272 | single nucleotide variant | NM_032869.4(NUDCD1):c.709A>G (p.Ile237Val) | not specified [RCV004652620] | uncertain significance | 8 | 109289865 | 109289865 | Human | | name |
| 407521730 | CV3462277 | single nucleotide variant | NM_015332.4(NUDCD3):c.308C>T (p.Ala103Val) | not specified [RCV004652625] | uncertain significance | 7 | 44485169 | 44485169 | Human | | name |
| 407521733 | CV3462279 | single nucleotide variant | NM_015332.4(NUDCD3):c.907G>A (p.Ala303Thr) | not specified [RCV004652626] | uncertain significance | 7 | 44392365 | 44392365 | Human | | name |
| 407477514 | CV3462280 | single nucleotide variant | NM_015332.4(NUDCD3):c.713T>C (p.Met238Thr) | not specified [RCV004638826] | uncertain significance | 7 | 44404513 | 44404513 | Human | | name |
| 596938353 | CV3550196 | single nucleotide variant | NM_015332.4(NUDCD3):c.938A>C (p.His313Pro) | not provided [RCV004813498] | likely pathogenic | 7 | 44392334 | 44392334 | Human | | name |
| 597643619 | CV3573512 | single nucleotide variant | NM_032869.4(NUDCD1):c.431G>A (p.Arg144His) | not specified [RCV004832637] | uncertain significance | 8 | 109296412 | 109296412 | Human | | name |
| 597709534 | CV3573513 | single nucleotide variant | NM_032869.4(NUDCD1):c.792T>A (p.Asn264Lys) | not specified [RCV004840685] | uncertain significance | 8 | 109289782 | 109289782 | Human | | name |
| 597709553 | CV3573517 | single nucleotide variant | NM_015332.4(NUDCD3):c.694A>G (p.Asn232Asp) | not specified [RCV004840687] | uncertain significance | 7 | 44404532 | 44404532 | Human | | name |
| 598233691 | CV3995060 | single nucleotide variant | NM_032869.4(NUDCD1):c.379G>A (p.Val127Ile) | not specified [RCV005381757] | uncertain significance | 8 | 109296464 | 109296464 | Human | | name |
| 598233698 | CV3995061 | single nucleotide variant | NM_032869.4(NUDCD1):c.896A>T (p.Lys299Met) | not specified [RCV005381758] | uncertain significance | 8 | 109281100 | 109281100 | Human | | name |
| 598265576 | CV3995065 | single nucleotide variant | NM_145266.6(NUDCD2):c.368C>T (p.Thr123Ile) | not specified [RCV005387970] | uncertain significance | 5 | 163456951 | 163456951 | Human | | name |
| 598265588 | CV3995068 | single nucleotide variant | NM_015332.4(NUDCD3):c.475G>C (p.Ala159Pro) | not specified [RCV005387972] | uncertain significance | 7 | 44485002 | 44485002 | Human | | name |
| 156375749 | CV2210297 | single nucleotide variant | NM_032869.4(NUDCD1):c.1202C>G (p.Pro401Arg) | not specified [RCV004089460] | uncertain significance | 8 | 109271102 | 109271102 | Human | | name |
| 155976273 | CV2211369 | single nucleotide variant | NM_032869.4(NUDCD1):c.1102G>A (p.Glu368Lys) | not specified [RCV004090288] | uncertain significance | 8 | 109275423 | 109275423 | Human | | name |
| 155976437 | CV2211390 | single nucleotide variant | NM_032869.4(NUDCD1):c.1582A>G (p.Thr528Ala) | not specified [RCV004090307] | uncertain significance | 8 | 109243179 | 109243179 | Human | | name |
| 156042593 | CV2215782 | single nucleotide variant | NM_032869.4(NUDCD1):c.1259T>C (p.Leu420Ser) | not specified [RCV004095377] | uncertain significance | 8 | 109271045 | 109271045 | Human | | name |
| 156173553 | CV2247609 | single nucleotide variant | NM_015332.4(NUDCD3):c.1070G>A (p.Gly357Glu) | not specified [RCV004108901] | uncertain significance | 7 | 44386027 | 44386027 | Human | | name |
| 156092348 | CV2256665 | single nucleotide variant | NM_032869.4(NUDCD1):c.1309G>A (p.Gly437Arg) | not specified [RCV004118846] | uncertain significance | 8 | 109245472 | 109245472 | Human | | name |
| 156201289 | CV2313137 | single nucleotide variant | NM_032869.4(NUDCD1):c.1477A>G (p.Lys493Glu) | not specified [RCV004161401] | uncertain significance | 8 | 109243284 | 109243284 | Human | | name |
| 155976341 | CV2342762 | single nucleotide variant | NM_032869.4(NUDCD1):c.1001G>C (p.Ser334Thr) | not specified [RCV004189806] | uncertain significance | 8 | 109280995 | 109280995 | Human | | name |
| 156252235 | CV2369017 | single nucleotide variant | NM_032869.4(NUDCD1):c.1576A>C (p.Met526Leu) | not specified [RCV004207955] | uncertain significance | 8 | 109243185 | 109243185 | Human | | name |
| 401732637 | CV2675145 | single nucleotide variant | NM_032869.4(NUDCD1):c.1337T>C (p.Ile446Thr) | not specified [RCV004289923] | uncertain significance | 8 | 109245444 | 109245444 | Human | | name |
| 401753131 | CV2725199 | single nucleotide variant | NM_032869.4(NUDCD1):c.1376A>T (p.His459Leu) | not specified [RCV004321721] | uncertain significance | 8 | 109245405 | 109245405 | Human | | name |
| 401858015 | CV2774146 | single nucleotide variant | NM_032869.4(NUDCD1):c.1510A>C (p.Asn504His) | not specified [RCV004345736] | uncertain significance | 8 | 109243251 | 109243251 | Human | | name |
| 401891993 | CV2780778 | single nucleotide variant | NM_032869.4(NUDCD1):c.1144C>A (p.Arg382Ser) | not specified [RCV004352101] | uncertain significance | 8 | 109275381 | 109275381 | Human | | name |
| 405728963 | CV3355836 | single nucleotide variant | NM_032869.4(NUDCD1):c.1020G>C (p.Glu340Asp) | not specified [RCV004496132] | uncertain significance | 8 | 109280976 | 109280976 | Human | | name |
| 405728979 | CV3355838 | single nucleotide variant | NM_032869.4(NUDCD1):c.1733A>G (p.Lys578Arg) | not specified [RCV004496134] | uncertain significance | 8 | 109243028 | 109243028 | Human | | name |
| 407521713 | CV3462271 | single nucleotide variant | NM_032869.4(NUDCD1):c.1444A>G (p.Thr482Ala) | not specified [RCV004652619] | uncertain significance | 8 | 109245337 | 109245337 | Human | | name |
| 407521719 | CV3462273 | single nucleotide variant | NM_032869.4(NUDCD1):c.1661A>T (p.Asp554Val) | not specified [RCV004652621] | uncertain significance | 8 | 109243100 | 109243100 | Human | | name |
| 407521727 | CV3462276 | single nucleotide variant | NM_015332.4(NUDCD3):c.1030G>A (p.Gly344Ser) | not specified [RCV004652624] | uncertain significance | 7 | 44386067 | 44386067 | Human | | name |
| 597643632 | CV3573516 | single nucleotide variant | NM_015332.4(NUDCD3):c.1037G>A (p.Arg346Gln) | not specified [RCV004832639] | uncertain significance | 7 | 44386060 | 44386060 | Human | | name |
| 598233707 | CV3995062 | single nucleotide variant | NM_032869.4(NUDCD1):c.1432G>C (p.Glu478Gln) | not specified [RCV005381759] | uncertain significance | 8 | 109245349 | 109245349 | Human | | name |
| 598233714 | CV3995063 | single nucleotide variant | NM_032869.4(NUDCD1):c.1543C>T (p.Arg515Cys) | not specified [RCV005381760] | uncertain significance | 8 | 109243218 | 109243218 | Human | | name |
| 598265571 | CV3995064 | single nucleotide variant | NM_032869.4(NUDCD1):c.1114G>C (p.Asp372His) | not specified [RCV005387969] | uncertain significance | 8 | 109275411 | 109275411 | Human | | name |
| 598233742 | CV3995070 | single nucleotide variant | NM_015332.4(NUDCD3):c.1052T>C (p.Met351Thr) | not specified [RCV005381763] | uncertain significance | 7 | 44386045 | 44386045 | Human | | name |
| 8632779 | CV87994 | single nucleotide variant | NM_001128211.1(NUDCD1):c.904C>T (p.His302Tyr) | Malignant melanoma [RCV000068086] | not provided | 8 | 109281005 | 109281005 | Human | | name |
