| 405265915 | CV3220970 | single nucleotide variant | NM_017886.4(ULK4):c.896+5T>G | ULK4-related disorder [RCV003969121] | likely benign | 3 | 41912802 | 41912802 | Human | | name , trait , alternate_id |
| 12896890 | CV389621 | single nucleotide variant | NM_017886.4(ULK4):c.803+3A>C | not provided [RCV004708913]|not specified [RCV000455956] | benign | 3 | 41915974 | 41915974 | Human | | name |
| 405290843 | CV3197137 | single nucleotide variant | NM_017886.4(ULK4):c.1764+3G>A | ULK4-related disorder [RCV003984699] | likely benign | 3 | 41835861 | 41835861 | Human | | name , trait , alternate_id |
| 12896441 | CV389560 | single nucleotide variant | NM_017886.4(ULK4):c.1288-9A>T | not provided [RCV004708912]|not specified [RCV000455343] | benign | 3 | 41898501 | 41898501 | Human | | name |
| 12895948 | CV389595 | single nucleotide variant | NM_017886.4(ULK4):c.1349-5C>G | not provided [RCV004710070]|not specified [RCV000454672] | benign | 3 | 41897008 | 41897008 | Human | | name |
| 15137504 | CV778994 | single nucleotide variant | NM_017886.4(ULK4):c.1183-8C>A | not provided [RCV000965631] | benign | 3 | 41900837 | 41900837 | Human | | name |
| 12896924 | CV389570 | single nucleotide variant | NM_017886.4(ULK4):c.1577+10G>A | not provided [RCV004708911]|not specified [RCV000455999] | benign | 3 | 41895508 | 41895508 | Human | | name |
| 405283897 | CV3199704 | single nucleotide variant | NM_017886.4(ULK4):c.165C>T (p.His55=) | ULK4-related disorder [RCV003979367] | likely benign | 3 | 41938171 | 41938171 | Human | | name , trait , alternate_id |
| 405805540 | CV3348248 | single nucleotide variant | NM_017886.4(ULK4):c.12T>A (p.Phe4Leu) | not specified [RCV004479769] | uncertain significance | 3 | 41954748 | 41954748 | Human | | name |
| 408384754 | CV3503476 | deletion | NM_017886.4(ULK4):c.2687-10_2687-9del | ULK4-related disorder [RCV004732081] | likely benign | 3 | 41705160 | 41705161 | Human | | name , trait , alternate_id |
| 401926333 | CV2827288 | single nucleotide variant | NM_017886.4(ULK4):c.903C>T (p.Asn301=) | not provided [RCV003437774] | likely benign | 3 | 41911653 | 41911653 | Human | | name |
| 405276885 | CV3192537 | single nucleotide variant | NM_017886.4(ULK4):c.876C>T (p.Ser292=) | ULK4-related disorder [RCV003917309] | likely benign | 3 | 41912827 | 41912827 | Human | | name , trait , alternate_id |
| 405805587 | CV3348270 | single nucleotide variant | NM_017886.4(ULK4):c.59A>G (p.Lys20Arg) | not specified [RCV004479791] | uncertain significance | 3 | 41954701 | 41954701 | Human | | name |
| 596945603 | CV3547958 | single nucleotide variant | NM_017886.4(ULK4):c.424T>C (p.Leu142=) | not provided [RCV004809289] | likely benign | 3 | 41931961 | 41931961 | Human | | name |
| 596945891 | CV3547999 | single nucleotide variant | NM_017886.4(ULK4):c.435G>T (p.Val145=) | not provided [RCV004809330] | likely benign | 3 | 41931950 | 41931950 | Human | | name |
| 597790186 | CV3632664 | single nucleotide variant | NM_017886.4(ULK4):c.30C>G (p.Ile10Met) | not specified [RCV004876284] | uncertain significance | 3 | 41954730 | 41954730 | Human | | name |
| 15123285 | CV748258 | single nucleotide variant | NM_017886.4(ULK4):c.537C>T (p.Val179=) | not provided [RCV000918794] | likely benign | 3 | 41931848 | 41931848 | Human | | name |
| 401741470 | CV2677367 | single nucleotide variant | NM_017886.4(ULK4):c.272A>G (p.Glu91Gly) | not specified [RCV004289449] | uncertain significance | 3 | 41935907 | 41935907 | Human | | name |
| 401922198 | CV2827286 | single nucleotide variant | NM_017886.4(ULK4):c.2532G>A (p.Leu844=) | not provided [RCV003433530] | likely benign | 3 | 41715492 | 41715492 | Human | | name |
| 401926332 | CV2827287 | single nucleotide variant | NM_017886.4(ULK4):c.2217T>C (p.Arg739=) | ULK4-related disorder [RCV003929125]|not provided [RCV003437773] | likely benign | 3 | 41754465 | 41754465 | Human | | name , trait , alternate_id |
| 405285195 | CV3202562 | single nucleotide variant | NM_017886.4(ULK4):c.2541C>T (p.Pro847=) | ULK4-related disorder [RCV003909819] | likely benign | 3 | 41715483 | 41715483 | Human | | name , trait , alternate_id |
| 405294328 | CV3214796 | single nucleotide variant | NM_017886.4(ULK4):c.2388T>C (p.Asn796=) | ULK4-related disorder [RCV003934212] | likely benign | 3 | 41717795 | 41717795 | Human | | name , trait , alternate_id |
| 405271203 | CV3218988 | single nucleotide variant | NM_017886.4(ULK4):c.2649T>C (p.Ser883=) | ULK4-related disorder [RCV003971718] | likely benign | 3 | 41705291 | 41705291 | Human | | name , trait , alternate_id |
| 405278102 | CV3221749 | single nucleotide variant | NM_017886.4(ULK4):c.1056T>C (p.Gly352=) | ULK4-related disorder [RCV003976335] | benign | 3 | 41911346 | 41911346 | Human | | name , trait , alternate_id |
| 405805538 | CV3348247 | single nucleotide variant | NM_017886.4(ULK4):c.121C>G (p.Pro41Ala) | not specified [RCV004479768] | uncertain significance | 3 | 41954639 | 41954639 | Human | | name |
| 407454450 | CV3489219 | single nucleotide variant | NM_017886.4(ULK4):c.152G>A (p.Arg51His) | not specified [RCV004685085] | likely benign | 3 | 41938184 | 41938184 | Human | | name |
| 597720585 | CV3632669 | single nucleotide variant | NM_017886.4(ULK4):c.202A>G (p.Ser68Gly) | not specified [RCV004887840] | uncertain significance | 3 | 41938134 | 41938134 | Human | | name |
| 12896448 | CV389558 | single nucleotide variant | NM_017886.4(ULK4):c.1599A>G (p.Val533=) | not provided [RCV004708910]|not specified [RCV000455353] | benign | 3 | 41883931 | 41883931 | Human | | name |
| 12896559 | CV389597 | single nucleotide variant | NM_017886.4(ULK4):c.116A>G (p.Lys39Arg) | not provided [RCV004708915]|not specified [RCV000455513] | benign | 3 | 41954644 | 41954644 | Human | | name |
| 598190900 | CV3925501 | single nucleotide variant | NM_017886.4(ULK4):c.142C>T (p.Arg48Cys) | not specified [RCV005288274] | uncertain significance | 3 | 41938194 | 41938194 | Human | | name |
| 15156748 | CV708852 | single nucleotide variant | NM_017886.4(ULK4):c.1626T>C (p.Ala542=) | ULK4-related disorder [RCV003972886]|not provided [RCV000969173] | benign|likely benign | 3 | 41883904 | 41883904 | Human | | name , trait , alternate_id |
| 150336539 | CV1165673 | single nucleotide variant | NM_017886.4(ULK4):c.417C>G (p.Asn139Lys) | not provided [RCV001531999] | likely benign | 3 | 41931968 | 41931968 | Human | | name |
| 156209616 | CV2250235 | single nucleotide variant | NM_017886.4(ULK4):c.334C>T (p.Leu112Phe) | not specified [RCV004117022] | uncertain significance | 3 | 41935845 | 41935845 | Human | | name |
| 156172585 | CV2267932 | single nucleotide variant | NM_017886.4(ULK4):c.978C>G (p.His326Gln) | not specified [RCV004136222] | uncertain significance | 3 | 41911578 | 41911578 | Human | | name |
| 155919368 | CV2333183 | single nucleotide variant | NM_017886.4(ULK4):c.901A>C (p.Asn301His) | not specified [RCV004194472] | uncertain significance | 3 | 41911655 | 41911655 | Human | | name |
| 401728040 | CV2685770 | single nucleotide variant | NM_017886.4(ULK4):c.935A>G (p.Lys312Arg) | not specified [RCV004294761] | uncertain significance | 3 | 41911621 | 41911621 | Human | | name |
| 401737397 | CV2695792 | single nucleotide variant | NM_017886.4(ULK4):c.736C>T (p.Arg246Cys) | not specified [RCV004308082] | uncertain significance | 3 | 41916044 | 41916044 | Human | | name |
| 401744059 | CV2696927 | single nucleotide variant | NM_017886.4(ULK4):c.728A>G (p.Asp243Gly) | not specified [RCV004292927] | uncertain significance | 3 | 41916052 | 41916052 | Human | | name |
| 401922199 | CV2827289 | single nucleotide variant | NM_017886.4(ULK4):c.493G>A (p.Asp165Asn) | ULK4-related disorder [RCV003929126]|not provided [RCV003433531] | likely benign | 3 | 41931892 | 41931892 | Human | | name , trait , alternate_id |
| 405286565 | CV3192234 | single nucleotide variant | NM_017886.4(ULK4):c.3250C>T (p.Leu1084=) | ULK4-related disorder [RCV003924136] | likely benign | 3 | 41463230 | 41463230 | Human | | name , trait , alternate_id |
| 405805578 | CV3348266 | single nucleotide variant | NM_017886.4(ULK4):c.364A>G (p.Ile122Val) | not specified [RCV004479787] | uncertain significance | 3 | 41935815 | 41935815 | Human | | name |
| 405805582 | CV3348268 | single nucleotide variant | NM_017886.4(ULK4):c.415A>G (p.Asn139Asp) | not specified [RCV004479789] | uncertain significance | 3 | 41931970 | 41931970 | Human | | name |
| 405805589 | CV3348271 | single nucleotide variant | NM_017886.4(ULK4):c.665A>G (p.Glu222Gly) | not specified [RCV004479792] | uncertain significance | 3 | 41918519 | 41918519 | Human | | name |
| 405805591 | CV3348272 | single nucleotide variant | NM_017886.4(ULK4):c.784C>A (p.Gln262Lys) | not specified [RCV004479793] | uncertain significance | 3 | 41915996 | 41915996 | Human | | name |
| 405805593 | CV3348273 | single nucleotide variant | NM_017886.4(ULK4):c.815C>T (p.Thr272Ile) | not specified [RCV004479794] | uncertain significance | 3 | 41912888 | 41912888 | Human | | name |
| 407454457 | CV3489224 | single nucleotide variant | NM_017886.4(ULK4):c.956A>G (p.Gln319Arg) | not specified [RCV004685089] | uncertain significance | 3 | 41911600 | 41911600 | Human | | name |
| 597790160 | CV3632654 | single nucleotide variant | NM_017886.4(ULK4):c.422G>T (p.Cys141Phe) | not specified [RCV004876277] | uncertain significance | 3 | 41931963 | 41931963 | Human | | name |
| 597790175 | CV3632660 | single nucleotide variant | NM_017886.4(ULK4):c.494A>G (p.Asp165Gly) | not specified [RCV004876281] | uncertain significance | 3 | 41931891 | 41931891 | Human | | name |
| 12896110 | CV389563 | single nucleotide variant | NM_017886.4(ULK4):c.670A>G (p.Ile224Val) | not provided [RCV004708914]|not specified [RCV000454894] | benign | 3 | 41918514 | 41918514 | Human | | name |
| 598266522 | CV3925495 | single nucleotide variant | NM_017886.4(ULK4):c.578G>A (p.Gly193Asp) | not specified [RCV005301959] | uncertain significance | 3 | 41919782 | 41919782 | Human | | name |
| 598190893 | CV3925499 | single nucleotide variant | NM_017886.4(ULK4):c.911A>C (p.Glu304Ala) | not specified [RCV005288273] | uncertain significance | 3 | 41911645 | 41911645 | Human | | name |
| 598190908 | CV3925504 | single nucleotide variant | NM_017886.4(ULK4):c.520A>G (p.Ser174Gly) | not specified [RCV005288275] | uncertain significance | 3 | 41931865 | 41931865 | Human | | name |
| 598266552 | CV3925505 | single nucleotide variant | NM_017886.4(ULK4):c.815C>G (p.Thr272Arg) | not specified [RCV005301966] | uncertain significance | 3 | 41912888 | 41912888 | Human | | name |
| 15137498 | CV708850 | single nucleotide variant | NM_017886.4(ULK4):c.3411A>G (p.Ser1137=) | not provided [RCV000965630] | benign | 3 | 41455578 | 41455578 | Human | | name |
| 15169727 | CV708851 | single nucleotide variant | NM_017886.4(ULK4):c.3201G>A (p.Ser1067=) | not provided [RCV000971870] | benign|likely benign | 3 | 41566050 | 41566050 | Human | | name |
| 156243505 | CV2210949 | single nucleotide variant | NM_017886.4(ULK4):c.2272T>C (p.Tyr758His) | ULK4-related disorder [RCV003928898]|not specified [RCV004086023] | likely benign|uncertain significance | 3 | 41754410 | 41754410 | Human | | name , trait , alternate_id |
| 156331856 | CV2220589 | single nucleotide variant | NM_017886.4(ULK4):c.1090C>T (p.Arg364Cys) | not specified [RCV004097783] | uncertain significance | 3 | 41907937 | 41907937 | Human | | name |
| 156283213 | CV2249738 | single nucleotide variant | NM_017886.4(ULK4):c.2890A>G (p.Asn964Asp) | not specified [RCV004122508] | uncertain significance | 3 | 41681596 | 41681596 | Human | | name |
| 11049694 | CV225810 | single nucleotide variant | NM_017886.4(ULK4):c.2887G>A (p.Val963Met) | Intellectual disability, moderate [RCV000209892]|ULK4-related disorder [RCV003917854] | likely benign|uncertain significance | 3 | 41681599 | 41681599 | Human | 2 | name , trait , alternate_id |
| 11049704 | CV225811 | single nucleotide variant | NM_017886.4(ULK4):c.2584C>T (p.Arg862Ter) | Intellectual disability, moderate [RCV000209944]|ULK4-related disorder [RCV003907778] | likely benign|uncertain significance | 3 | 41715287 | 41715287 | Human | 2 | name , trait , alternate_id |
| 11049690 | CV225812 | single nucleotide variant | NM_017886.4(ULK4):c.2056G>A (p.Val686Ile) | Intellectual disability, moderate [RCV000209867]|ULK4-related disorder [RCV003927888]|not provided [RCV003430770] | likely benign|uncertain significance | 3 | 41789798 | 41789798 | Human | 2 | name , trait , alternate_id |
| 156334569 | CV2263358 | single nucleotide variant | NM_017886.4(ULK4):c.2942A>G (p.Asn981Ser) | not specified [RCV004133625] | likely benign | 3 | 41681544 | 41681544 | Human | | name |
| 156048235 | CV2271708 | single nucleotide variant | NM_017886.4(ULK4):c.2461A>T (p.Ile821Phe) | not specified [RCV004130555] | uncertain significance | 3 | 41715563 | 41715563 | Human | | name |
| 156289151 | CV2299305 | single nucleotide variant | NM_017886.4(ULK4):c.2258T>C (p.Phe753Ser) | not specified [RCV004152626] | uncertain significance | 3 | 41754424 | 41754424 | Human | | name |
| 156263086 | CV2314945 | single nucleotide variant | NM_017886.4(ULK4):c.2021G>A (p.Arg674Lys) | not specified [RCV004171048] | uncertain significance | 3 | 41789833 | 41789833 | Human | | name |
| 156301805 | CV2319426 | single nucleotide variant | NM_017886.4(ULK4):c.1753G>A (p.Val585Ile) | not specified [RCV004185013] | uncertain significance | 3 | 41835875 | 41835875 | Human | | name |
| 156149203 | CV2321910 | single nucleotide variant | NM_017886.4(ULK4):c.1578A>G (p.Ile526Met) | not specified [RCV004173377] | uncertain significance | 3 | 41883952 | 41883952 | Human | | name |
| 155963574 | CV2330342 | single nucleotide variant | NM_017886.4(ULK4):c.1648G>A (p.Val550Ile) | not specified [RCV004180918] | uncertain significance | 3 | 41883882 | 41883882 | Human | | name |
| 156052567 | CV2336749 | single nucleotide variant | NM_017886.4(ULK4):c.2273A>T (p.Tyr758Phe) | not specified [RCV004196986] | uncertain significance | 3 | 41754409 | 41754409 | Human | | name |
| 156070055 | CV2341162 | single nucleotide variant | NM_017886.4(ULK4):c.2413C>T (p.Leu805Phe) | not specified [RCV004181636] | uncertain significance | 3 | 41717770 | 41717770 | Human | | name |
| 156253123 | CV2366137 | single nucleotide variant | NM_017886.4(ULK4):c.2780C>T (p.Thr927Met) | not specified [RCV004210170] | uncertain significance | 3 | 41705058 | 41705058 | Human | | name |
| 156048888 | CV2378133 | single nucleotide variant | NM_017886.4(ULK4):c.1627G>A (p.Glu543Lys) | not specified [RCV004233050] | uncertain significance | 3 | 41883903 | 41883903 | Human | | name |
| 329377988 | CV2460954 | single nucleotide variant | NM_017886.4(ULK4):c.2525T>G (p.Leu842Arg) | not specified [RCV004265114] | uncertain significance | 3 | 41715499 | 41715499 | Human | | name |
| 329353679 | CV2467051 | single nucleotide variant | NM_017886.4(ULK4):c.1241A>T (p.Tyr414Phe) | not specified [RCV004282791] | uncertain significance | 3 | 41900771 | 41900771 | Human | | name |
| 401766272 | CV2679629 | single nucleotide variant | NM_017886.4(ULK4):c.2491C>G (p.Arg831Gly) | not specified [RCV004282105] | uncertain significance | 3 | 41715533 | 41715533 | Human | | name |
| 401772817 | CV2712925 | single nucleotide variant | NM_017886.4(ULK4):c.2209A>G (p.Ile737Val) | not specified [RCV004314326] | likely benign | 3 | 41754473 | 41754473 | Human | | name |
| 401763174 | CV2720222 | single nucleotide variant | NM_017886.4(ULK4):c.1096A>T (p.Thr366Ser) | not specified [RCV004325560] | uncertain significance | 3 | 41907931 | 41907931 | Human | | name |
| 401895941 | CV2779320 | single nucleotide variant | NM_017886.4(ULK4):c.2182A>C (p.Ile728Leu) | not specified [RCV004350987] | uncertain significance | 3 | 41789672 | 41789672 | Human | | name |
| 401864485 | CV2781786 | single nucleotide variant | NM_017886.4(ULK4):c.1783C>A (p.Pro595Thr) | not specified [RCV004356747] | uncertain significance | 3 | 41819488 | 41819488 | Human | | name |
| 405279901 | CV3191529 | single nucleotide variant | NM_017886.4(ULK4):c.1808T>C (p.Leu603Ser) | ULK4-related disorder [RCV003919680] | benign | 3 | 41819463 | 41819463 | Human | | name , trait , alternate_id |
| 405276654 | CV3193435 | single nucleotide variant | NM_017886.4(ULK4):c.1042A>G (p.Ser348Gly) | ULK4-related disorder [RCV003974603] | benign | 3 | 41911360 | 41911360 | Human | | name , trait , alternate_id |
| 405284253 | CV3196672 | single nucleotide variant | NM_017886.4(ULK4):c.2143G>A (p.Ala715Thr) | ULK4-related disorder [RCV003979578] | benign | 3 | 41789711 | 41789711 | Human | 4 | name , trait , alternate_id |
| 405290968 | CV3197224 | single nucleotide variant | NM_017886.4(ULK4):c.2551G>A (p.Val851Ile) | ULK4-related disorder [RCV003984787] | benign | 3 | 41715473 | 41715473 | Human | 4 | name , trait , alternate_id |
| 405284014 | CV3200483 | single nucleotide variant | NM_017886.4(ULK4):c.1706A>G (p.Lys569Arg) | ULK4-related disorder [RCV003979505] | benign | 3 | 41835922 | 41835922 | Human | | name , trait , alternate_id |
| 405282670 | CV3212986 | single nucleotide variant | NM_017886.4(ULK4):c.1160A>G (p.Gln387Arg) | ULK4-related disorder [RCV003957091] | likely benign | 3 | 41907867 | 41907867 | Human | | name , trait , alternate_id |
| 405295457 | CV3216045 | single nucleotide variant | NM_017886.4(ULK4):c.2849T>C (p.Phe950Ser) | ULK4-related disorder [RCV003937406] | likely benign | 3 | 41681637 | 41681637 | Human | | name , trait , alternate_id |
| 405287630 | CV3217832 | single nucleotide variant | NM_017886.4(ULK4):c.2530T>A (p.Leu844Met) | ULK4-related disorder [RCV003981955] | benign | 3 | 41715494 | 41715494 | Human | | name , trait , alternate_id |
| 405805534 | CV3348245 | single nucleotide variant | NM_017886.4(ULK4):c.1034G>A (p.Arg345Gln) | not specified [RCV004479766] | uncertain significance | 3 | 41911368 | 41911368 | Human | | name |
| 405805536 | CV3348246 | single nucleotide variant | NM_017886.4(ULK4):c.1070C>A (p.Ser357Tyr) | not specified [RCV004479767] | uncertain significance | 3 | 41911332 | 41911332 | Human | | name |
| 405805542 | CV3348249 | single nucleotide variant | NM_017886.4(ULK4):c.1421C>T (p.Ser474Phe) | not specified [RCV004479770] | uncertain significance | 3 | 41896931 | 41896931 | Human | | name |
| 405805544 | CV3348250 | single nucleotide variant | NM_017886.4(ULK4):c.1520A>C (p.His507Pro) | not specified [RCV004479771] | uncertain significance | 3 | 41896832 | 41896832 | Human | | name |
| 405805546 | CV3348251 | single nucleotide variant | NM_017886.4(ULK4):c.1660A>G (p.Ile554Val) | not specified [RCV004479772] | uncertain significance | 3 | 41835968 | 41835968 | Human | | name |
| 405805548 | CV3348252 | single nucleotide variant | NM_017886.4(ULK4):c.1681A>G (p.Ile561Val) | not specified [RCV004479773] | uncertain significance | 3 | 41835947 | 41835947 | Human | | name |
| 405805550 | CV3348253 | single nucleotide variant | NM_017886.4(ULK4):c.1786A>G (p.Arg596Gly) | not specified [RCV004479774] | uncertain significance | 3 | 41819485 | 41819485 | Human | | name |
| 405805553 | CV3348254 | single nucleotide variant | NM_017886.4(ULK4):c.2346C>G (p.Asp782Glu) | not specified [RCV004479775] | uncertain significance | 3 | 41717837 | 41717837 | Human | | name |
| 405805555 | CV3348255 | single nucleotide variant | NM_017886.4(ULK4):c.2566G>C (p.Val856Leu) | not specified [RCV004479776] | uncertain significance | 3 | 41715458 | 41715458 | Human | | name |
| 405805557 | CV3348256 | single nucleotide variant | NM_017886.4(ULK4):c.2666C>T (p.Thr889Met) | not specified [RCV004479777] | uncertain significance | 3 | 41705274 | 41705274 | Human | | name |
| 405805559 | CV3348257 | single nucleotide variant | NM_017886.4(ULK4):c.2715G>T (p.Lys905Asn) | not specified [RCV004479778] | uncertain significance | 3 | 41705123 | 41705123 | Human | | name |
| 405805561 | CV3348258 | single nucleotide variant | NM_017886.4(ULK4):c.2740A>T (p.Ile914Leu) | not specified [RCV004479779] | uncertain significance | 3 | 41705098 | 41705098 | Human | | name |
| 405805563 | CV3348259 | single nucleotide variant | NM_017886.4(ULK4):c.2858G>A (p.Arg953Gln) | not specified [RCV004479780] | uncertain significance | 3 | 41681628 | 41681628 | Human | | name |
| 405805565 | CV3348260 | single nucleotide variant | NM_017886.4(ULK4):c.2993T>C (p.Leu998Pro) | not specified [RCV004479781] | uncertain significance | 3 | 41663685 | 41663685 | Human | | name |
| 407454444 | CV3489216 | single nucleotide variant | NM_017886.4(ULK4):c.1265C>T (p.Thr422Ile) | not specified [RCV004685082] | uncertain significance | 3 | 41900747 | 41900747 | Human | | name |
| 407454446 | CV3489217 | single nucleotide variant | NM_017886.4(ULK4):c.1580G>A (p.Arg527Gln) | not specified [RCV004685083] | uncertain significance | 3 | 41883950 | 41883950 | Human | | name |
| 407454448 | CV3489218 | single nucleotide variant | NM_017886.4(ULK4):c.2774G>A (p.Arg925His) | not specified [RCV004685084] | uncertain significance | 3 | 41705064 | 41705064 | Human | | name |
| 407462463 | CV3489220 | single nucleotide variant | NM_017886.4(ULK4):c.2009C>T (p.Ser670Leu) | not specified [RCV004687970] | uncertain significance | 3 | 41800133 | 41800133 | Human | | name |
| 407454452 | CV3489221 | single nucleotide variant | NM_017886.4(ULK4):c.2060T>C (p.Ile687Thr) | not specified [RCV004685086] | uncertain significance | 3 | 41789794 | 41789794 | Human | | name |
| 407454456 | CV3489223 | single nucleotide variant | NM_017886.4(ULK4):c.1776A>T (p.Lys592Asn) | not specified [RCV004685088] | uncertain significance | 3 | 41819495 | 41819495 | Human | | name |
| 596946961 | CV3547020 | single nucleotide variant | NM_017886.4(ULK4):c.1710A>C (p.Leu570Phe) | not provided [RCV004810826] | likely benign | 3 | 41835918 | 41835918 | Human | | name |
| 597720541 | CV3632655 | single nucleotide variant | NM_017886.4(ULK4):c.2216G>A (p.Arg739His) | not specified [RCV004887836] | uncertain significance | 3 | 41754466 | 41754466 | Human | | name |
| 597790164 | CV3632656 | single nucleotide variant | NM_017886.4(ULK4):c.1033C>T (p.Arg345Trp) | not specified [RCV004876278] | uncertain significance | 3 | 41911369 | 41911369 | Human | | name |
| 597720552 | CV3632658 | single nucleotide variant | NM_017886.4(ULK4):c.2461A>G (p.Ile821Val) | not specified [RCV004887837] | uncertain significance | 3 | 41715563 | 41715563 | Human | | name |
| 597720563 | CV3632661 | single nucleotide variant | NM_017886.4(ULK4):c.2039C>A (p.Pro680His) | not specified [RCV004887838] | uncertain significance | 3 | 41789815 | 41789815 | Human | | name |
| 597790180 | CV3632662 | single nucleotide variant | NM_017886.4(ULK4):c.1106C>A (p.Thr369Asn) | not specified [RCV004876282] | uncertain significance | 3 | 41907921 | 41907921 | Human | | name |
| 597790183 | CV3632663 | single nucleotide variant | NM_017886.4(ULK4):c.1805C>T (p.Pro602Leu) | not specified [RCV004876283] | uncertain significance | 3 | 41819466 | 41819466 | Human | | name |
| 597720574 | CV3632665 | single nucleotide variant | NM_017886.4(ULK4):c.1891A>T (p.Asn631Tyr) | not specified [RCV004887839] | uncertain significance | 3 | 41800251 | 41800251 | Human | | name |
| 597790191 | CV3632666 | single nucleotide variant | NM_017886.4(ULK4):c.2585G>A (p.Arg862Gln) | not specified [RCV004876285] | uncertain significance | 3 | 41715286 | 41715286 | Human | | name |
| 597790194 | CV3632667 | single nucleotide variant | NM_017886.4(ULK4):c.2809G>A (p.Val937Met) | not specified [RCV004876286] | uncertain significance | 3 | 41681777 | 41681777 | Human | | name |
| 12896000 | CV389585 | single nucleotide variant | NM_017886.4(ULK4):c.1624G>A (p.Ala542Thr) | not provided [RCV004708909]|not specified [RCV000454745] | benign | 3 | 41883906 | 41883906 | Human | | name |
| 12896756 | CV389614 | single nucleotide variant | NM_017886.4(ULK4):c.1918T>G (p.Ser640Ala) | not provided [RCV004708908]|not specified [RCV000455782] | benign | 3 | 41800224 | 41800224 | Human | | name |
| 598190879 | CV3925492 | single nucleotide variant | NM_017886.4(ULK4):c.1931T>C (p.Ile644Thr) | not specified [RCV005288271] | uncertain significance | 3 | 41800211 | 41800211 | Human | | name |
| 598190886 | CV3925493 | single nucleotide variant | NM_017886.4(ULK4):c.2404T>C (p.Cys802Arg) | not specified [RCV005288272] | uncertain significance | 3 | 41717779 | 41717779 | Human | | name |
| 598266530 | CV3925497 | single nucleotide variant | NM_017886.4(ULK4):c.1616C>T (p.Ser539Leu) | not specified [RCV005301961] | uncertain significance | 3 | 41883914 | 41883914 | Human | | name |
| 598266543 | CV3925502 | single nucleotide variant | NM_017886.4(ULK4):c.1988C>T (p.Ser663Phe) | not specified [RCV005301964] | uncertain significance | 3 | 41800154 | 41800154 | Human | | name |
| 598266547 | CV3925503 | single nucleotide variant | NM_017886.4(ULK4):c.2398T>C (p.Ser800Pro) | not specified [RCV005301965] | uncertain significance | 3 | 41717785 | 41717785 | Human | | name |
| 598190915 | CV3925506 | single nucleotide variant | NM_017886.4(ULK4):c.1586A>G (p.Lys529Arg) | not specified [RCV005288276] | uncertain significance | 3 | 41883944 | 41883944 | Human | | name |
| 8630827 | CV85982 | single nucleotide variant | NM_017886.2(ULK4):c.2362C>T (p.Pro788Ser) | Malignant melanoma [RCV000066066] | not provided | 3 | 41717821 | 41717821 | Human | | name |
| 156181189 | CV2201795 | single nucleotide variant | NM_017886.4(ULK4):c.3781G>A (p.Ala1261Thr) | not specified [RCV004082232] | uncertain significance | 3 | 41246976 | 41246976 | Human | | name |
| 156134901 | CV2213250 | single nucleotide variant | NM_017886.4(ULK4):c.3122A>T (p.Glu1041Val) | not specified [RCV004085470] | uncertain significance | 3 | 41566129 | 41566129 | Human | | name |
| 156094753 | CV2213456 | single nucleotide variant | NM_017886.4(ULK4):c.3745C>T (p.Arg1249Trp) | not specified [RCV004087430] | uncertain significance | 3 | 41249508 | 41249508 | Human | | name |
| 156062395 | CV2240064 | single nucleotide variant | NM_017886.4(ULK4):c.3776A>G (p.Asp1259Gly) | not specified [RCV004110842] | uncertain significance | 3 | 41246981 | 41246981 | Human | | name |
| 156298442 | CV2240956 | single nucleotide variant | NM_017886.4(ULK4):c.3752C>T (p.Ala1251Val) | not specified [RCV004102233] | uncertain significance | 3 | 41249501 | 41249501 | Human | | name |
| 156246538 | CV2276765 | single nucleotide variant | NM_017886.4(ULK4):c.3073C>T (p.Leu1025Phe) | not specified [RCV004146547] | uncertain significance | 3 | 41615716 | 41615716 | Human | | name |
| 155957922 | CV2282132 | single nucleotide variant | NM_017886.4(ULK4):c.3620T>C (p.Leu1207Pro) | not specified [RCV004138867] | uncertain significance | 3 | 41398137 | 41398137 | Human | | name |
| 156116492 | CV2282912 | single nucleotide variant | NM_017886.4(ULK4):c.3574C>T (p.Pro1192Ser) | not specified [RCV004143554] | uncertain significance | 3 | 41398183 | 41398183 | Human | | name |
| 156185326 | CV2294940 | single nucleotide variant | NM_017886.4(ULK4):c.3560A>G (p.Tyr1187Cys) | not specified [RCV004156089] | uncertain significance | 3 | 41398197 | 41398197 | Human | | name |
| 156001836 | CV2296453 | single nucleotide variant | NM_017886.4(ULK4):c.3454A>G (p.Arg1152Gly) | not specified [RCV004148194] | uncertain significance | 3 | 41455535 | 41455535 | Human | | name |
| 156094513 | CV2310016 | single nucleotide variant | NM_017886.4(ULK4):c.3185T>A (p.Val1062Asp) | not specified [RCV004163157] | uncertain significance | 3 | 41566066 | 41566066 | Human | | name |
| 155931038 | CV2362432 | single nucleotide variant | NM_017886.4(ULK4):c.3374T>C (p.Ile1125Thr) | not specified [RCV004213053] | uncertain significance | 3 | 41463106 | 41463106 | Human | | name |
| 156152317 | CV2394847 | single nucleotide variant | NM_017886.4(ULK4):c.3515T>C (p.Ile1172Thr) | not specified [RCV004234507] | uncertain significance | 3 | 41398242 | 41398242 | Human | | name |
| 329364808 | CV2443931 | single nucleotide variant | NM_017886.4(ULK4):c.3817G>A (p.Val1273Ile) | not specified [RCV004258260] | uncertain significance | 3 | 41246940 | 41246940 | Human | | name |
| 329361023 | CV2463209 | single nucleotide variant | NM_017886.4(ULK4):c.3205A>G (p.Met1069Val) | not specified [RCV004274986] | uncertain significance | 3 | 41566046 | 41566046 | Human | | name |
| 329398765 | CV2471699 | single nucleotide variant | NM_017886.4(ULK4):c.3602A>G (p.Glu1201Gly) | not specified [RCV004286979] | uncertain significance | 3 | 41398155 | 41398155 | Human | | name |
| 401756235 | CV2687045 | single nucleotide variant | NM_017886.4(ULK4):c.3762T>A (p.Ser1254Arg) | not specified [RCV004304367] | uncertain significance | 3 | 41249491 | 41249491 | Human | | name |
| 401764423 | CV2727939 | single nucleotide variant | NM_017886.4(ULK4):c.3159T>G (p.Ser1053Arg) | not specified [RCV004324116] | uncertain significance | 3 | 41566092 | 41566092 | Human | | name |
| 401878693 | CV2767516 | single nucleotide variant | NM_017886.4(ULK4):c.3316C>G (p.Pro1106Ala) | not specified [RCV004343677] | likely benign | 3 | 41463164 | 41463164 | Human | | name |
| 401877541 | CV2769492 | single nucleotide variant | NM_017886.4(ULK4):c.3218A>T (p.Tyr1073Phe) | not specified [RCV004357464] | uncertain significance | 3 | 41566033 | 41566033 | Human | | name |
| 405805567 | CV3348261 | single nucleotide variant | NM_017886.4(ULK4):c.3006C>G (p.Asp1002Glu) | not specified [RCV004479782] | uncertain significance | 3 | 41663672 | 41663672 | Human | | name |
| 405805570 | CV3348262 | single nucleotide variant | NM_017886.4(ULK4):c.3041C>T (p.Ala1014Val) | not specified [RCV004479783] | uncertain significance | 3 | 41663637 | 41663637 | Human | | name |
| 405805572 | CV3348263 | single nucleotide variant | NM_017886.4(ULK4):c.3404C>G (p.Ser1135Cys) | not specified [RCV004479784] | uncertain significance | 3 | 41455585 | 41455585 | Human | | name |
| 405805574 | CV3348264 | single nucleotide variant | NM_017886.4(ULK4):c.3442C>G (p.Leu1148Val) | not specified [RCV004479785] | uncertain significance | 3 | 41455547 | 41455547 | Human | | name |
| 405805576 | CV3348265 | single nucleotide variant | NM_017886.4(ULK4):c.3571A>G (p.Asn1191Asp) | not specified [RCV004479786] | uncertain significance | 3 | 41398186 | 41398186 | Human | | name |
| 405805580 | CV3348267 | single nucleotide variant | NM_017886.4(ULK4):c.3733C>T (p.Arg1245Trp) | not specified [RCV004479788] | uncertain significance | 3 | 41249520 | 41249520 | Human | | name |
| 407454454 | CV3489222 | single nucleotide variant | NM_017886.4(ULK4):c.3470T>C (p.Leu1157Pro) | not specified [RCV004685087] | uncertain significance | 3 | 41455519 | 41455519 | Human | | name |
| 597790156 | CV3632653 | single nucleotide variant | NM_017886.4(ULK4):c.3679A>T (p.Ile1227Phe) | not specified [RCV004876276] | uncertain significance | 3 | 41249574 | 41249574 | Human | | name |
| 597790167 | CV3632657 | single nucleotide variant | NM_017886.4(ULK4):c.3040G>A (p.Ala1014Thr) | not specified [RCV004876279] | uncertain significance | 3 | 41663638 | 41663638 | Human | | name |
| 597790172 | CV3632659 | single nucleotide variant | NM_017886.4(ULK4):c.3623C>T (p.Thr1208Ile) | not specified [RCV004876280] | uncertain significance | 3 | 41398134 | 41398134 | Human | | name |
| 597790199 | CV3632668 | single nucleotide variant | NM_017886.4(ULK4):c.3119T>C (p.Leu1040Pro) | not specified [RCV004876287] | uncertain significance | 3 | 41615670 | 41615670 | Human | | name |
| 598266518 | CV3925494 | single nucleotide variant | NM_017886.4(ULK4):c.3689A>G (p.Asn1230Ser) | not specified [RCV005301958] | uncertain significance | 3 | 41249564 | 41249564 | Human | | name |
| 598266526 | CV3925496 | single nucleotide variant | NM_017886.4(ULK4):c.3629A>G (p.Lys1210Arg) | not specified [RCV005301960] | uncertain significance | 3 | 41398128 | 41398128 | Human | | name |
| 598266538 | CV3925500 | single nucleotide variant | NM_017886.4(ULK4):c.3550G>A (p.Val1184Ile) | not specified [RCV005301963] | uncertain significance | 3 | 41398207 | 41398207 | Human | | name |
| 8630826 | CV85981 | single nucleotide variant | NM_017886.2(ULK4):c.3190T>G (p.Cys1064Gly) | Malignant melanoma [RCV000066065] | not provided | 3 | 41566061 | 41566061 | Human | | name |
