Umodl1 Variant Search Result - Rat Genome Database

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213 records found for search term Umodl1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150455277	CV1232424	single nucleotide variant	NM_001004416.3(UMODL1):c.790+3T>G	not provided [RCV001648438]	benign	21	42088483	42088483	Human		name
15186181	CV745134	single nucleotide variant	NM_001004416.3(UMODL1):c.791-10T>C	not provided [RCV000908737]	likely benign	21	42090288	42090288	Human		name
156315114	CV2192857	single nucleotide variant	NM_001004416.3(UMODL1):c.1899+68G>A	not specified [RCV004069428]	uncertain significance	21	42111189	42111189	Human		name
156228770	CV2199430	single nucleotide variant	NM_001004416.3(UMODL1):c.1899+43C>T	not specified [RCV004070993]	uncertain significance	21	42111164	42111164	Human		name
156305750	CV2338901	single nucleotide variant	NM_001004416.3(UMODL1):c.1899+97G>A	not specified [RCV004184494]	uncertain significance	21	42111218	42111218	Human		name
155995721	CV2375849	single nucleotide variant	NM_001004416.3(UMODL1):c.1899+26G>T	not specified [RCV004217698]	uncertain significance	21	42111147	42111147	Human		name
401780710	CV2685676	single nucleotide variant	NM_001004416.3(UMODL1):c.1899+38G>C	not specified [RCV004296730]	uncertain significance	21	42111159	42111159	Human		name
401779006	CV2702014	single nucleotide variant	NM_001004416.3(UMODL1):c.1899+87C>A	not specified [RCV004320601]	uncertain significance	21	42111208	42111208	Human		name
405805632	CV3348291	single nucleotide variant	NM_001004416.3(UMODL1):c.1899+67G>A	not specified [RCV004479812]	uncertain significance	21	42111188	42111188	Human		name
597790203	CV3632681	single nucleotide variant	NM_001004416.3(UMODL1):c.1900-48A>G	not specified [RCV004876288]	uncertain significance	21	42111458	42111458	Human		name
156219852	CV2226020	single nucleotide variant	NM_001004416.3(UMODL1):c.1899+147C>G	not specified [RCV004105177]	uncertain significance	21	42111268	42111268	Human		name
155977393	CV2231900	single nucleotide variant	NM_001004416.3(UMODL1):c.1899+158T>A	not specified [RCV004098690]	uncertain significance	21	42111279	42111279	Human		name
156115542	CV2273364	single nucleotide variant	NM_001004416.3(UMODL1):c.1900-162C>T	not specified [RCV004132138]	uncertain significance	21	42111344	42111344	Human		name
156049194	CV2336500	single nucleotide variant	NM_001004416.3(UMODL1):c.1899+110A>G	not specified [RCV004194710]	uncertain significance	21	42111231	42111231	Human		name
329392201	CV2441308	single nucleotide variant	NM_001004416.3(UMODL1):c.1899+113C>T	not specified [RCV004257124]	uncertain significance	21	42111234	42111234	Human		name
405805635	CV3348292	single nucleotide variant	NM_001004416.3(UMODL1):c.1899+130A>C	not specified [RCV004479813]	uncertain significance	21	42111251	42111251	Human		name
405805637	CV3348293	single nucleotide variant	NM_001004416.3(UMODL1):c.1900-147C>A	not specified [RCV004479814]	likely benign	21	42111359	42111359	Human		name
597790222	CV3632688	single nucleotide variant	NM_001004416.3(UMODL1):c.1899+187G>A	not specified [RCV004876293]	uncertain significance	21	42111308	42111308	Human		name
597790229	CV3632692	single nucleotide variant	NM_001004416.3(UMODL1):c.1899+155A>T	not specified [RCV004876295]	uncertain significance	21	42111276	42111276	Human		name
156101028	CV2367596	single nucleotide variant	NM_001004416.3(UMODL1):c.14C>T (p.Ser5Leu)	not specified [RCV004211523]	likely benign	21	42071330	42071330	Human		name
401920132	CV2824780	single nucleotide variant	NM_001004416.3(UMODL1):c.255C>T (p.Pro85=)	not provided [RCV003431514]	likely benign	21	42076183	42076183	Human		name
15170304	CV705710	variation	NM_001004416.3(UMODL1):c.1676= (p.Met559=)	not provided [RCV000949625]	benign	21	42110898	42110898	Human		name
401920134	CV2824781	single nucleotide variant	NM_001004416.3(UMODL1):c.420T>A (p.Pro140=)	not provided [RCV003431515]	likely benign	21	42084184	42084184	Human		name
401930582	CV2824782	single nucleotide variant	NM_001004416.3(UMODL1):c.846C>T (p.Cys282=)	not provided [RCV003440580]	likely benign	21	42090353	42090353	Human		name
401930583	CV2824783	single nucleotide variant	NM_001004416.3(UMODL1):c.907C>A (p.Arg303=)	not provided [RCV003440581]	likely benign	21	42090414	42090414	Human		name
597790270	CV3632707	single nucleotide variant	NM_001004416.3(UMODL1):c.83G>C (p.Gly28Ala)	not specified [RCV004876306]	uncertain significance	21	42076011	42076011	Human		name
597790287	CV3632715	single nucleotide variant	NM_001004416.3(UMODL1):c.44C>T (p.Ala15Val)	not specified [RCV004876311]	uncertain significance	21	42071360	42071360	Human		name
598266572	CV3925515	single nucleotide variant	NM_001004416.3(UMODL1):c.67G>A (p.Gly23Ser)	not specified [RCV005301972]	uncertain significance	21	42071383	42071383	Human		name
156183467	CV2198515	single nucleotide variant	NM_001004416.3(UMODL1):c.203G>A (p.Arg68Lys)	not specified [RCV004075545]	uncertain significance	21	42076131	42076131	Human		name
156283940	CV2348980	single nucleotide variant	NM_001004416.3(UMODL1):c.294A>T (p.Glu98Asp)	not specified [RCV004203411]	uncertain significance	21	42076222	42076222	Human		name
156105485	CV2352540	single nucleotide variant	NM_001004416.3(UMODL1):c.219G>A (p.Met73Ile)	not specified [RCV004203041]	uncertain significance	21	42076147	42076147	Human		name
155987646	CV2363865	single nucleotide variant	NM_001004416.3(UMODL1):c.292G>A (p.Glu98Lys)	not specified [RCV004218840]	uncertain significance	21	42076220	42076220	Human		name
401930585	CV2824785	single nucleotide variant	NM_001004416.3(UMODL1):c.2115C>T (p.Ser705=)	not provided [RCV003440583]	likely benign	21	42113583	42113583	Human		name
401930586	CV2824787	single nucleotide variant	NM_001004416.3(UMODL1):c.2517C>T (p.Asp839=)	not provided [RCV003440584]	likely benign	21	42119152	42119152	Human		name
405805640	CV3348295	single nucleotide variant	NM_001004416.3(UMODL1):c.268G>A (p.Val90Met)	not specified [RCV004479816]	uncertain significance	21	42076196	42076196	Human		name
597790233	CV3632695	single nucleotide variant	NM_001004416.3(UMODL1):c.125C>G (p.Thr42Ser)	not specified [RCV004876296]	uncertain significance	21	42076053	42076053	Human		name
15163477	CV705711	single nucleotide variant	NM_001004416.3(UMODL1):c.2985C>T (p.Ile995=)	not provided [RCV000948095]	benign	21	42122988	42122988	Human		name
15176772	CV717221	single nucleotide variant	NM_001004416.3(UMODL1):c.1797G>A (p.Pro599=)	not provided [RCV000973264]	benign	21	42111019	42111019	Human		name
15182444	CV728920	single nucleotide variant	NM_001004416.3(UMODL1):c.1959C>T (p.Thr653=)	not provided [RCV000885993]	likely benign	21	42111565	42111565	Human		name
15121549	CV757836	single nucleotide variant	NM_001004416.3(UMODL1):c.1365C>T (p.Ile455=)	not provided [RCV000918501]	benign	21	42103933	42103933	Human		name
15114416	CV757837	single nucleotide variant	NM_001004416.3(UMODL1):c.2592C>T (p.Ile864=)	not provided [RCV000917273]	likely benign	21	42119227	42119227	Human		name
156320766	CV2197395	single nucleotide variant	NM_001004416.3(UMODL1):c.623C>A (p.Pro208Gln)	not specified [RCV004081134]	uncertain significance	21	42088313	42088313	Human		name
156117356	CV2231856	single nucleotide variant	NM_001004416.3(UMODL1):c.334G>C (p.Gly112Arg)	not specified [RCV004098656]	likely benign	21	42084098	42084098	Human		name
156124717	CV2237415	single nucleotide variant	NM_001004416.3(UMODL1):c.637G>A (p.Val213Ile)	not specified [RCV004106383]	likely benign	21	42088327	42088327	Human		name
155961244	CV2285502	single nucleotide variant	NM_001004416.3(UMODL1):c.627G>A (p.Met209Ile)	not specified [RCV004139348]	uncertain significance	21	42088317	42088317	Human		name
156049739	CV2315876	single nucleotide variant	NM_001004416.3(UMODL1):c.451G>A (p.Gly151Arg)	not specified [RCV004171652]	uncertain significance	21	42084215	42084215	Human		name
156062478	CV2316525	single nucleotide variant	NM_001004416.3(UMODL1):c.515A>G (p.Asn172Ser)	not specified [RCV004169992]	uncertain significance	21	42085324	42085324	Human		name
155908245	CV2354598	single nucleotide variant	NM_001004416.3(UMODL1):c.778G>A (p.Val260Ile)	not specified [RCV004202569]	likely benign	21	42088468	42088468	Human		name
156144778	CV2383954	single nucleotide variant	NM_001004416.3(UMODL1):c.580C>A (p.His194Asn)	not specified [RCV004224936]	uncertain significance	21	42085389	42085389	Human		name
329392309	CV2470589	single nucleotide variant	NM_001004416.3(UMODL1):c.427G>A (p.Glu143Lys)	not specified [RCV004273589]	uncertain significance	21	42084191	42084191	Human		name
401748821	CV2706035	single nucleotide variant	NM_001004416.3(UMODL1):c.376C>A (p.Pro126Thr)	not specified [RCV004314736]	uncertain significance	21	42084140	42084140	Human		name
401766377	CV2725463	single nucleotide variant	NM_001004416.3(UMODL1):c.506C>T (p.Ser169Phe)	not specified [RCV004320095]	likely benign	21	42085315	42085315	Human		name
401774389	CV2727826	single nucleotide variant	NM_001004416.3(UMODL1):c.560T>G (p.Val187Gly)	not specified [RCV004323848]	uncertain significance	21	42085369	42085369	Human		name
401757747	CV2731424	single nucleotide variant	NM_001004416.3(UMODL1):c.302G>A (p.Gly101Asp)	not specified [RCV004330785]	uncertain significance	21	42076230	42076230	Human		name
401779107	CV2733125	single nucleotide variant	NM_001004416.3(UMODL1):c.634A>G (p.Thr212Ala)	not specified [RCV004332056]	likely benign	21	42088324	42088324	Human		name
401855839	CV2757530	single nucleotide variant	NM_001004416.3(UMODL1):c.650A>G (p.His217Arg)	not specified [RCV004340907]	uncertain significance	21	42088340	42088340	Human		name
401861054	CV2772691	single nucleotide variant	NM_001004416.3(UMODL1):c.651C>G (p.His217Gln)	not specified [RCV004355424]	uncertain significance	21	42088341	42088341	Human		name
401930587	CV2824788	single nucleotide variant	NM_001004416.3(UMODL1):c.3537T>G (p.Pro1179=)	not provided [RCV003440585]	likely benign	21	42127678	42127678	Human		name
405265489	CV3185704	single nucleotide variant	NM_001004416.3(UMODL1):c.424C>T (p.Leu142Phe)	not provided [RCV003886268]	likely benign	21	42084188	42084188	Human		name
405805653	CV3348301	single nucleotide variant	NM_001004416.3(UMODL1):c.334G>A (p.Gly112Arg)	not specified [RCV004479822]	likely benign	21	42084098	42084098	Human		name
405805681	CV3348314	single nucleotide variant	NM_001004416.3(UMODL1):c.449G>C (p.Gly150Ala)	not specified [RCV004479835]	uncertain significance	21	42084213	42084213	Human		name
405805683	CV3348315	single nucleotide variant	NM_001004416.3(UMODL1):c.497C>G (p.Pro166Arg)	not specified [RCV004479836]	uncertain significance	21	42085306	42085306	Human		name
405805686	CV3348316	single nucleotide variant	NM_001004416.3(UMODL1):c.863C>T (p.Ser288Leu)	not specified [RCV004479837]	uncertain significance	21	42090370	42090370	Human		name
407454469	CV3489231	single nucleotide variant	NM_001004416.3(UMODL1):c.686G>A (p.Arg229Gln)	not specified [RCV004685096]	uncertain significance	21	42088376	42088376	Human		name
407462467	CV3489232	single nucleotide variant	NM_001004416.3(UMODL1):c.808T>C (p.Tyr270His)	not specified [RCV004687971]	uncertain significance	21	42090315	42090315	Human		name
407454475	CV3489235	single nucleotide variant	NM_001004416.3(UMODL1):c.649C>T (p.His217Tyr)	not specified [RCV004685099]	uncertain significance	21	42088339	42088339	Human		name
407454479	CV3489237	single nucleotide variant	NM_001004416.3(UMODL1):c.581A>G (p.His194Arg)	not specified [RCV004685101]	uncertain significance	21	42085390	42085390	Human		name
407454483	CV3489239	single nucleotide variant	NM_001004416.3(UMODL1):c.653C>T (p.Ser218Leu)	not specified [RCV004685103]	uncertain significance	21	42088343	42088343	Human		name
597720618	CV3632687	single nucleotide variant	NM_001004416.3(UMODL1):c.707G>A (p.Arg236Gln)	not specified [RCV004887843]	likely benign	21	42088397	42088397	Human		name
597790245	CV3632699	single nucleotide variant	NM_001004416.3(UMODL1):c.750T>G (p.Ile250Met)	not specified [RCV004876299]	uncertain significance	21	42088440	42088440	Human		name
598190922	CV3925511	single nucleotide variant	NM_001004416.3(UMODL1):c.852C>G (p.Asn284Lys)	not specified [RCV005288277]	uncertain significance	21	42090359	42090359	Human		name
598190938	CV3925514	single nucleotide variant	NM_001004416.3(UMODL1):c.899C>T (p.Thr300Met)	not specified [RCV005288279]	uncertain significance	21	42090406	42090406	Human		name
598190945	CV3925516	single nucleotide variant	NM_001004416.3(UMODL1):c.725A>G (p.Asp242Gly)	not specified [RCV005288280]	uncertain significance	21	42088415	42088415	Human		name
8628616	CV83760	single nucleotide variant	NM_001004416.2(UMODL1):c.484C>T (p.Pro162Ser)	Malignant melanoma [RCV000063841]	not provided	21	42085293	42085293	Human		name
156313030	CV2196449	single nucleotide variant	NM_001004416.3(UMODL1):c.2615T>C (p.Val872Ala)	not specified [RCV004073750]	uncertain significance	21	42119250	42119250	Human		name
156274795	CV2202668	single nucleotide variant	NM_001004416.3(UMODL1):c.1796C>T (p.Pro599Leu)	not specified [RCV004082918]	likely benign	21	42111018	42111018	Human		name
156231991	CV2227646	single nucleotide variant	NM_001004416.3(UMODL1):c.1296C>A (p.His432Gln)	not specified [RCV004094050]	uncertain significance	21	42102275	42102275	Human		name
156029142	CV2238288	single nucleotide variant	NM_001004416.3(UMODL1):c.2919C>A (p.Ser973Arg)	not specified [RCV004113366]	uncertain significance	21	42122922	42122922	Human		name
155923193	CV2251880	single nucleotide variant	NM_001004416.3(UMODL1):c.2971G>A (p.Val991Met)	not specified [RCV004119859]	uncertain significance	21	42122974	42122974	Human		name
156314183	CV2257120	single nucleotide variant	NM_001004416.3(UMODL1):c.1364T>C (p.Ile455Thr)	not specified [RCV004123081]	uncertain significance	21	42103932	42103932	Human		name
156040837	CV2261333	single nucleotide variant	NM_001004416.3(UMODL1):c.1261G>T (p.Val421Leu)	not specified [RCV004129981]	uncertain significance	21	42102240	42102240	Human		name
156259443	CV2277828	single nucleotide variant	NM_001004416.3(UMODL1):c.1993C>T (p.Arg665Trp)	not specified [RCV004147249]	likely benign	21	42111599	42111599	Human		name
155994440	CV2277974	single nucleotide variant	NM_001004416.3(UMODL1):c.1423G>A (p.Gly475Arg)	not specified [RCV004141218]	uncertain significance	21	42103991	42103991	Human		name
156067591	CV2284828	single nucleotide variant	NM_001004416.3(UMODL1):c.2915C>G (p.Thr972Ser)	not specified [RCV004143002]	uncertain significance	21	42122918	42122918	Human		name
156073155	CV2299161	single nucleotide variant	NM_001004416.3(UMODL1):c.1604A>G (p.Gln535Arg)	not specified [RCV004152504]	likely benign	21	42109646	42109646	Human		name
156091931	CV2302698	single nucleotide variant	NM_001004416.3(UMODL1):c.1699A>G (p.Thr567Ala)	not specified [RCV004162635]	uncertain significance	21	42110921	42110921	Human		name
156258480	CV2304868	single nucleotide variant	NM_001004416.3(UMODL1):c.2117T>C (p.Ile706Thr)	not specified [RCV004168788]	uncertain significance	21	42113585	42113585	Human		name
156298952	CV2325915	single nucleotide variant	NM_001004416.3(UMODL1):c.1097C>A (p.Ala366Asp)	not specified [RCV004174090]	uncertain significance	21	42099091	42099091	Human		name
156395432	CV2329187	single nucleotide variant	NM_001004416.3(UMODL1):c.1018C>A (p.His340Asn)	not specified [RCV004173941]	uncertain significance	21	42099012	42099012	Human		name
156395434	CV2329188	single nucleotide variant	NM_001004416.3(UMODL1):c.2750C>A (p.Thr917Asn)	not specified [RCV004173942]	uncertain significance	21	42121147	42121147	Human		name
155919232	CV2333158	single nucleotide variant	NM_001004416.3(UMODL1):c.1723G>T (p.Gly575Cys)	not specified [RCV004194448]	uncertain significance	21	42110945	42110945	Human		name
155916667	CV2336184	single nucleotide variant	NM_001004416.3(UMODL1):c.2945G>A (p.Arg982Gln)	not specified [RCV004189777]	uncertain significance	21	42122948	42122948	Human		name
156345435	CV2356223	single nucleotide variant	NM_001004416.3(UMODL1):c.1034G>A (p.Arg345Gln)	not specified [RCV004206038]	likely benign	21	42099028	42099028	Human		name
156010939	CV2362187	single nucleotide variant	NM_001004416.3(UMODL1):c.2366C>T (p.Ala789Val)	not specified [RCV004209985]	uncertain significance	21	42115876	42115876	Human		name
156402232	CV2363606	single nucleotide variant	NM_001004416.3(UMODL1):c.2461C>G (p.Leu821Val)	not specified [RCV004216561]	uncertain significance	21	42115971	42115971	Human		name
156085321	CV2366154	single nucleotide variant	NM_001004416.3(UMODL1):c.1835G>T (p.Arg612Ile)	not specified [RCV004210185]	uncertain significance	21	42111057	42111057	Human		name
156085868	CV2366236	single nucleotide variant	NM_001004416.3(UMODL1):c.2423G>A (p.Arg808His)	not specified [RCV004210252]	uncertain significance	21	42115933	42115933	Human		name
155929409	CV2369733	single nucleotide variant	NM_001004416.3(UMODL1):c.2219T>C (p.Met740Thr)	not specified [RCV004215128]	likely benign	21	42113687	42113687	Human		name
156098397	CV2370773	single nucleotide variant	NM_001004416.3(UMODL1):c.2857A>G (p.Thr953Ala)	not specified [RCV004209170]	uncertain significance	21	42122860	42122860	Human		name
155989920	CV2371988	single nucleotide variant	NM_001004416.3(UMODL1):c.2723G>A (p.Cys908Tyr)	not specified [RCV004221664]	uncertain significance	21	42121120	42121120	Human		name
156044764	CV2381654	single nucleotide variant	NM_001004416.3(UMODL1):c.1042C>T (p.Arg348Trp)	not specified [RCV004232125]	uncertain significance	21	42099036	42099036	Human		name
156348629	CV2383155	single nucleotide variant	NM_001004416.3(UMODL1):c.2744G>A (p.Arg915Gln)	not specified [RCV004219768]	uncertain significance	21	42121141	42121141	Human		name
156005246	CV2401070	single nucleotide variant	NM_001004416.3(UMODL1):c.2944C>T (p.Arg982Trp)	not specified [RCV004245642]	uncertain significance	21	42122947	42122947	Human		name
329369800	CV2424943	single nucleotide variant	NM_001004416.3(UMODL1):c.2566G>C (p.Val856Leu)	not specified [RCV004248817]	uncertain significance	21	42119201	42119201	Human		name
329361433	CV2437019	single nucleotide variant	NM_001004416.3(UMODL1):c.1610G>A (p.Arg537His)	not specified [RCV004260384]	uncertain significance	21	42109652	42109652	Human		name
329360352	CV2446690	single nucleotide variant	NM_001004416.3(UMODL1):c.2480G>A (p.Arg827Gln)	not specified [RCV004251574]	uncertain significance	21	42119115	42119115	Human		name
329385093	CV2454691	single nucleotide variant	NM_001004416.3(UMODL1):c.1783C>T (p.Pro595Ser)	not specified [RCV004269931]	uncertain significance	21	42111005	42111005	Human		name
401739445	CV2673288	single nucleotide variant	NM_001004416.3(UMODL1):c.1919T>C (p.Met640Thr)	not specified [RCV004286088]	likely benign	21	42111525	42111525	Human		name
401735958	CV2692240	single nucleotide variant	NM_001004416.3(UMODL1):c.1275C>G (p.Asp425Glu)	not specified [RCV004303718]	uncertain significance	21	42102254	42102254	Human		name
401730203	CV2700496	single nucleotide variant	NM_001004416.3(UMODL1):c.2519C>T (p.Ala840Val)	not specified [RCV004311126]	uncertain significance	21	42119154	42119154	Human		name
401876814	CV2767725	single nucleotide variant	NM_001004416.3(UMODL1):c.1252C>T (p.Arg418Cys)	not specified [RCV004345855]	uncertain significance	21	42102231	42102231	Human		name
401864465	CV2777852	single nucleotide variant	NM_001004416.3(UMODL1):c.1270C>G (p.Gln424Glu)	not specified [RCV004346037]	uncertain significance	21	42102249	42102249	Human		name
401864920	CV2791417	single nucleotide variant	NM_001004416.3(UMODL1):c.1684G>A (p.Gly562Arg)	not specified [RCV004358813]	uncertain significance	21	42110906	42110906	Human		name
401930584	CV2824784	single nucleotide variant	NM_001004416.3(UMODL1):c.1653T>G (p.Cys551Trp)	not provided [RCV003440582]	uncertain significance	21	42109695	42109695	Human		name
401920136	CV2824786	single nucleotide variant	NM_001004416.3(UMODL1):c.2368C>T (p.Arg790Trp)	not provided [RCV003431516]	likely benign	21	42115878	42115878	Human		name
405805618	CV3348284	single nucleotide variant	NM_001004416.3(UMODL1):c.1033C>T (p.Arg345Trp)	not specified [RCV004479805]	likely benign	21	42099027	42099027	Human		name
405805620	CV3348285	single nucleotide variant	NM_001004416.3(UMODL1):c.1091C>T (p.Ala364Val)	not specified [RCV004479806]	uncertain significance	21	42099085	42099085	Human		name
405805622	CV3348286	single nucleotide variant	NM_001004416.3(UMODL1):c.1499G>T (p.Arg500Leu)	not specified [RCV004479807]	uncertain significance	21	42104067	42104067	Human		name
405805624	CV3348287	single nucleotide variant	NM_001004416.3(UMODL1):c.1522T>C (p.Trp508Arg)	not specified [RCV004479808]	uncertain significance	21	42109564	42109564	Human		name
405805626	CV3348288	single nucleotide variant	NM_001004416.3(UMODL1):c.1630C>A (p.Pro544Thr)	not specified [RCV004479809]	uncertain significance	21	42109672	42109672	Human		name
405805628	CV3348289	single nucleotide variant	NM_001004416.3(UMODL1):c.1810G>A (p.Ala604Thr)	not specified [RCV004479810]	uncertain significance	21	42111032	42111032	Human		name
405805630	CV3348290	single nucleotide variant	NM_001004416.3(UMODL1):c.1888G>A (p.Val630Met)	not specified [RCV004479811]	uncertain significance	21	42111110	42111110	Human		name
405805638	CV3348294	single nucleotide variant	NM_001004416.3(UMODL1):c.2147G>C (p.Ser716Thr)	not specified [RCV004479815]	uncertain significance	21	42113615	42113615	Human		name
405805643	CV3348296	single nucleotide variant	NM_001004416.3(UMODL1):c.2314A>C (p.Lys772Gln)	not specified [RCV004479817]	uncertain significance	21	42113782	42113782	Human		name
405805645	CV3348297	single nucleotide variant	NM_001004416.3(UMODL1):c.2438A>C (p.Gln813Pro)	not specified [RCV004479818]	uncertain significance	21	42115948	42115948	Human		name
405805647	CV3348298	single nucleotide variant	NM_001004416.3(UMODL1):c.2734A>G (p.Thr912Ala)	not specified [RCV004479819]	uncertain significance	21	42121131	42121131	Human		name
405805649	CV3348299	single nucleotide variant	NM_001004416.3(UMODL1):c.2816G>A (p.Arg939Lys)	not specified [RCV004479820]	uncertain significance	21	42121213	42121213	Human		name
407454477	CV3489236	single nucleotide variant	NM_001004416.3(UMODL1):c.2539G>A (p.Val847Ile)	not specified [RCV004685100]	uncertain significance	21	42119174	42119174	Human		name
407454481	CV3489238	single nucleotide variant	NM_001004416.3(UMODL1):c.1205T>C (p.Val402Ala)	not specified [RCV004685102]	uncertain significance	21	42102184	42102184	Human		name
407454485	CV3489240	single nucleotide variant	NM_001004416.3(UMODL1):c.2990A>G (p.Lys997Arg)	not specified [RCV004685104]	uncertain significance	21	42122993	42122993	Human		name
407454487	CV3489241	single nucleotide variant	NM_001004416.3(UMODL1):c.1045G>C (p.Gly349Arg)	not specified [RCV004685105]	uncertain significance	21	42099039	42099039	Human		name
407462469	CV3489242	single nucleotide variant	NM_001004416.3(UMODL1):c.1640C>T (p.Ala547Val)	not specified [RCV004687972]	uncertain significance	21	42109682	42109682	Human		name
407462473	CV3489243	single nucleotide variant	NM_001004416.3(UMODL1):c.2228C>T (p.Pro743Leu)	not specified [RCV004687973]	uncertain significance	21	42113696	42113696	Human		name
407454489	CV3489244	single nucleotide variant	NM_001004416.3(UMODL1):c.2511C>A (p.His837Gln)	not specified [RCV004685106]	uncertain significance	21	42119146	42119146	Human		name
407454492	CV3489245	single nucleotide variant	NM_001004416.3(UMODL1):c.2170G>A (p.Glu724Lys)	not specified [RCV004685107]	uncertain significance	21	42113638	42113638	Human		name
407454493	CV3489246	single nucleotide variant	NM_001004416.3(UMODL1):c.1528G>A (p.Glu510Lys)	not specified [RCV004685108]	uncertain significance	21	42109570	42109570	Human		name
597790210	CV3632683	single nucleotide variant	NM_001004416.3(UMODL1):c.1559C>T (p.Ser520Leu)	not specified [RCV004876290]	uncertain significance	21	42109601	42109601	Human		name
597790218	CV3632686	single nucleotide variant	NM_001004416.3(UMODL1):c.2843A>C (p.Asn948Thr)	not specified [RCV004876292]	uncertain significance	21	42122846	42122846	Human		name
597790224	CV3632689	single nucleotide variant	NM_001004416.3(UMODL1):c.2791G>T (p.Asp931Tyr)	not specified [RCV004876294]	uncertain significance	21	42121188	42121188	Human		name
597720638	CV3632691	single nucleotide variant	NM_001004416.3(UMODL1):c.1232T>A (p.Leu411Gln)	not specified [RCV004887845]	uncertain significance	21	42102211	42102211	Human		name
597720648	CV3632693	single nucleotide variant	NM_001004416.3(UMODL1):c.1499G>A (p.Arg500Gln)	not specified [RCV004887846]	likely benign	21	42104067	42104067	Human		name
597720659	CV3632694	single nucleotide variant	NM_001004416.3(UMODL1):c.1960G>A (p.Gly654Ser)	not specified [RCV004887847]	uncertain significance	21	42111566	42111566	Human		name
597790241	CV3632697	single nucleotide variant	NM_001004416.3(UMODL1):c.2755G>A (p.Gly919Arg)	not specified [RCV004876298]	uncertain significance	21	42121152	42121152	Human		name
597720672	CV3632698	single nucleotide variant	NM_001004416.3(UMODL1):c.2555A>G (p.Asn852Ser)	not specified [RCV004887848]	uncertain significance	21	42119190	42119190	Human		name
597790248	CV3632700	single nucleotide variant	NM_001004416.3(UMODL1):c.1697C>T (p.Ala566Val)	not specified [RCV004876300]	uncertain significance	21	42110919	42110919	Human		name
597790252	CV3632701	single nucleotide variant	NM_001004416.3(UMODL1):c.1562C>T (p.Pro521Leu)	not specified [RCV004876301]	uncertain significance	21	42109604	42109604	Human		name
597720683	CV3632702	single nucleotide variant	NM_001004416.3(UMODL1):c.2486C>T (p.Ser829Phe)	not specified [RCV004887849]	uncertain significance	21	42119121	42119121	Human		name
597790262	CV3632705	single nucleotide variant	NM_001004416.3(UMODL1):c.2515G>C (p.Asp839His)	not specified [RCV004876304]	uncertain significance	21	42119150	42119150	Human		name
597790266	CV3632706	single nucleotide variant	NM_001004416.3(UMODL1):c.1532G>A (p.Cys511Tyr)	not specified [RCV004876305]	uncertain significance	21	42109574	42109574	Human		name
597790274	CV3632709	single nucleotide variant	NM_001004416.3(UMODL1):c.2153G>T (p.Gly718Val)	not specified [RCV004876307]	uncertain significance	21	42113621	42113621	Human		name
597790277	CV3632710	single nucleotide variant	NM_001004416.3(UMODL1):c.1850A>G (p.Asn617Ser)	not specified [RCV004876308]	likely benign	21	42111072	42111072	Human		name
597720701	CV3632711	single nucleotide variant	NM_001004416.3(UMODL1):c.2720A>C (p.Asp907Ala)	not specified [RCV004887851]	uncertain significance	21	42121117	42121117	Human		name
597790279	CV3632712	single nucleotide variant	NM_001004416.3(UMODL1):c.1093G>A (p.Val365Met)	not specified [RCV004876309]	uncertain significance	21	42099087	42099087	Human		name
597720709	CV3632713	single nucleotide variant	NM_001004416.3(UMODL1):c.1447C>G (p.Leu483Val)	not specified [RCV004887852]	uncertain significance	21	42104015	42104015	Human		name
597790283	CV3632714	single nucleotide variant	NM_001004416.3(UMODL1):c.1627A>G (p.Thr543Ala)	not specified [RCV004876310]	uncertain significance	21	42109669	42109669	Human		name
598266567	CV3925512	single nucleotide variant	NM_001004416.3(UMODL1):c.2369G>A (p.Arg790Gln)	not specified [RCV005301971]	likely benign	21	42115879	42115879	Human		name
598266576	CV3925517	single nucleotide variant	NM_001004416.3(UMODL1):c.1994G>A (p.Arg665Gln)	not specified [RCV005301973]	uncertain significance	21	42111600	42111600	Human		name
598266580	CV3925518	single nucleotide variant	NM_001004416.3(UMODL1):c.2192C>G (p.Ser731Cys)	not specified [RCV005301974]	uncertain significance	21	42113660	42113660	Human		name
598266585	CV3925519	single nucleotide variant	NM_001004416.3(UMODL1):c.1678G>T (p.Gly560Cys)	not specified [RCV005301975]	uncertain significance	21	42110900	42110900	Human		name
153001830	CV1682708	single nucleotide variant	NM_001004416.3(UMODL1):c.3905A>G (p.Tyr1302Cys)	not provided [RCV002251787]	uncertain significance	21	42137568	42137568	Human		name
10767902	CV221031	single nucleotide variant	NM_001004416.3(UMODL1):c.3655G>A (p.Val1219Ile)	Prostate cancer [RCV000205501]	uncertain significance	21	42127796	42127796	Human	2	name
155920928	CV2210930	single nucleotide variant	NM_001004416.3(UMODL1):c.3295G>A (p.Val1099Ile)	not specified [RCV004086008]	uncertain significance	21	42127007	42127007	Human		name
155925493	CV2211844	single nucleotide variant	NM_001004416.3(UMODL1):c.3176C>A (p.Thr1059Lys)	not specified [RCV004086668]	uncertain significance	21	42126373	42126373	Human		name
156273461	CV2247669	single nucleotide variant	NM_001004416.3(UMODL1):c.3946T>G (p.Phe1316Val)	not specified [RCV004115085]	uncertain significance	21	42137609	42137609	Human		name
156253198	CV2264558	single nucleotide variant	NM_001004416.3(UMODL1):c.3187G>C (p.Asp1063His)	not specified [RCV004132572]	uncertain significance	21	42126384	42126384	Human		name
156362922	CV2265633	single nucleotide variant	NM_001004416.3(UMODL1):c.3349C>A (p.Gln1117Lys)	not specified [RCV004124361]	uncertain significance	21	42127061	42127061	Human		name
156114950	CV2273256	single nucleotide variant	NM_001004416.3(UMODL1):c.3497G>A (p.Arg1166Gln)	not specified [RCV004132049]	uncertain significance	21	42127209	42127209	Human		name
156287239	CV2292157	single nucleotide variant	NM_001004416.3(UMODL1):c.3736A>T (p.Thr1246Ser)	not specified [RCV004160408]	uncertain significance	21	42129758	42129758	Human		name
156169562	CV2317090	single nucleotide variant	NM_001004416.3(UMODL1):c.3158A>G (p.Asn1053Ser)	not specified [RCV004174574]	uncertain significance	21	42126355	42126355	Human		name
156335248	CV2333501	single nucleotide variant	NM_001004416.3(UMODL1):c.3464C>T (p.Thr1155Met)	not specified [RCV004190195]	uncertain significance	21	42127176	42127176	Human		name
155923053	CV2340728	single nucleotide variant	NM_001004416.3(UMODL1):c.3317T>C (p.Leu1106Pro)	not specified [RCV004190397]	uncertain significance	21	42127029	42127029	Human		name
156304058	CV2341375	single nucleotide variant	NM_001004416.3(UMODL1):c.3898G>T (p.Gly1300Trp)	not specified [RCV004188777]	uncertain significance	21	42137561	42137561	Human		name
156115232	CV2349275	single nucleotide variant	NM_001004416.3(UMODL1):c.3496C>T (p.Arg1166Trp)	not specified [RCV004199222]	uncertain significance	21	42127208	42127208	Human		name
156127762	CV2351265	single nucleotide variant	NM_001004416.3(UMODL1):c.3881G>A (p.Arg1294His)	not specified [RCV004214111]	likely benign	21	42137544	42137544	Human		name
156389434	CV2373876	single nucleotide variant	NM_001004416.3(UMODL1):c.3952G>A (p.Glu1318Lys)	not specified [RCV004224809]	uncertain significance	21	42137615	42137615	Human		name
156036493	CV2373990	single nucleotide variant	NM_001004416.3(UMODL1):c.3652C>T (p.Arg1218Cys)	not specified [RCV004227120]	uncertain significance	21	42127793	42127793	Human		name
156215621	CV2386001	single nucleotide variant	NM_001004416.3(UMODL1):c.3013C>T (p.Arg1005Cys)	not specified [RCV004229067]	uncertain significance	21	42123016	42123016	Human		name
156172060	CV2400750	single nucleotide variant	NM_001004416.3(UMODL1):c.3854C>T (p.Ala1285Val)	not specified [RCV004242415]	uncertain significance	21	42137517	42137517	Human		name
329357540	CV2427758	single nucleotide variant	NM_001004416.3(UMODL1):c.3643T>A (p.Cys1215Ser)	not specified [RCV004252540]	uncertain significance	21	42127784	42127784	Human		name
329396907	CV2463625	single nucleotide variant	NM_001004416.3(UMODL1):c.3122G>A (p.Ser1041Asn)	not specified [RCV004277421]	uncertain significance	21	42123125	42123125	Human		name
329388772	CV2469562	single nucleotide variant	NM_001004416.3(UMODL1):c.3844G>A (p.Val1282Met)	not specified [RCV004282999]	uncertain significance	21	42137507	42137507	Human		name
401742344	CV2677564	single nucleotide variant	NM_001004416.3(UMODL1):c.3487A>G (p.Ser1163Gly)	not specified [RCV004291667]	uncertain significance	21	42127199	42127199	Human		name
401780987	CV2681850	single nucleotide variant	NM_001004416.3(UMODL1):c.3274G>A (p.Gly1092Ser)	not specified [RCV004296845]	uncertain significance	21	42126471	42126471	Human		name
401757902	CV2685624	single nucleotide variant	NM_001004416.3(UMODL1):c.3251A>G (p.Gln1084Arg)	not specified [RCV004294633]	likely benign	21	42126448	42126448	Human		name
401734336	CV2709459	single nucleotide variant	NM_001004416.3(UMODL1):c.3173C>A (p.Thr1058Asn)	not specified [RCV004318706]	uncertain significance	21	42126370	42126370	Human		name
401782873	CV2716021	single nucleotide variant	NM_001004416.3(UMODL1):c.3418G>C (p.Glu1140Gln)	not specified [RCV004323277]	uncertain significance	21	42127130	42127130	Human		name
401895060	CV2792752	single nucleotide variant	NM_001004416.3(UMODL1):c.3390C>G (p.Ser1130Arg)	not specified [RCV004365513]	uncertain significance	21	42127102	42127102	Human		name
401920138	CV2824789	single nucleotide variant	NM_001004416.3(UMODL1):c.3934A>G (p.Ser1312Gly)	not provided [RCV003431517]	uncertain significance	21	42137597	42137597	Human		name
405805655	CV3348302	single nucleotide variant	NM_001004416.3(UMODL1):c.3067T>G (p.Ser1023Ala)	not specified [RCV004479823]	uncertain significance	21	42123070	42123070	Human		name
405805657	CV3348303	single nucleotide variant	NM_001004416.3(UMODL1):c.3181A>G (p.Arg1061Gly)	not specified [RCV004479824]	uncertain significance	21	42126378	42126378	Human		name
405805659	CV3348304	single nucleotide variant	NM_001004416.3(UMODL1):c.3206T>A (p.Ile1069Asn)	not specified [RCV004479825]	uncertain significance	21	42126403	42126403	Human		name
405805661	CV3348305	single nucleotide variant	NM_001004416.3(UMODL1):c.3391G>A (p.Val1131Met)	not specified [RCV004479826]	uncertain significance	21	42127103	42127103	Human		name
405805664	CV3348306	single nucleotide variant	NM_001004416.3(UMODL1):c.3401G>T (p.Ser1134Ile)	not specified [RCV004479827]	uncertain significance	21	42127113	42127113	Human		name
405805666	CV3348307	single nucleotide variant	NM_001004416.3(UMODL1):c.3559G>T (p.Val1187Leu)	not specified [RCV004479828]	uncertain significance	21	42127700	42127700	Human		name
405805668	CV3348308	single nucleotide variant	NM_001004416.3(UMODL1):c.3655G>C (p.Val1219Leu)	not specified [RCV004479829]	uncertain significance	21	42127796	42127796	Human		name
405805670	CV3348309	single nucleotide variant	NM_001004416.3(UMODL1):c.3707G>A (p.Arg1236Gln)	not specified [RCV004479830]	uncertain significance	21	42129729	42129729	Human		name
405805672	CV3348310	single nucleotide variant	NM_001004416.3(UMODL1):c.3767G>A (p.Arg1256Gln)	not specified [RCV004479831]	uncertain significance	21	42129789	42129789	Human		name
405805675	CV3348311	single nucleotide variant	NM_001004416.3(UMODL1):c.3839T>C (p.Ile1280Thr)	not specified [RCV004479832]	uncertain significance	21	42137502	42137502	Human		name
405805677	CV3348312	single nucleotide variant	NM_001004416.3(UMODL1):c.3878T>C (p.Val1293Ala)	not specified [RCV004479833]	uncertain significance	21	42137541	42137541	Human		name
407454471	CV3489233	single nucleotide variant	NM_001004416.3(UMODL1):c.3880C>T (p.Arg1294Cys)	not specified [RCV004685097]	uncertain significance	21	42137543	42137543	Human		name
407454473	CV3489234	single nucleotide variant	NM_001004416.3(UMODL1):c.3325G>A (p.Ala1109Thr)	not specified [RCV004685098]	uncertain significance	21	42127037	42127037	Human		name
597720597	CV3632680	single nucleotide variant	NM_001004416.3(UMODL1):c.3538G>A (p.Val1180Met)	not specified [RCV004887841]	uncertain significance	21	42127679	42127679	Human		name
597790206	CV3632682	single nucleotide variant	NM_001004416.3(UMODL1):c.3706C>T (p.Arg1236Trp)	not specified [RCV004876289]	uncertain significance	21	42129728	42129728	Human		name
597790214	CV3632684	single nucleotide variant	NM_001004416.3(UMODL1):c.3001G>A (p.Ala1001Thr)	not specified [RCV004876291]	uncertain significance	21	42123004	42123004	Human		name
597720608	CV3632685	single nucleotide variant	NM_001004416.3(UMODL1):c.3558C>A (p.Asn1186Lys)	not specified [RCV004887842]	uncertain significance	21	42127699	42127699	Human		name
597720629	CV3632690	single nucleotide variant	NM_001004416.3(UMODL1):c.3322G>A (p.Gly1108Ser)	not specified [RCV004887844]	uncertain significance	21	42127034	42127034	Human		name
597790237	CV3632696	single nucleotide variant	NM_001004416.3(UMODL1):c.3090T>G (p.Asn1030Lys)	not specified [RCV004876297]	uncertain significance	21	42123093	42123093	Human		name
597790254	CV3632703	single nucleotide variant	NM_001004416.3(UMODL1):c.3047C>T (p.Ser1016Leu)	not specified [RCV004876302]	uncertain significance	21	42123050	42123050	Human		name
597790258	CV3632704	single nucleotide variant	NM_001004416.3(UMODL1):c.3358A>G (p.Ile1120Val)	not specified [RCV004876303]	uncertain significance	21	42127070	42127070	Human		name
597720693	CV3632708	single nucleotide variant	NM_001004416.3(UMODL1):c.3361G>A (p.Gly1121Arg)	not specified [RCV004887850]	uncertain significance	21	42127073	42127073	Human		name
597790291	CV3632716	single nucleotide variant	NM_001004416.3(UMODL1):c.3251A>T (p.Gln1084Leu)	not specified [RCV004876312]	uncertain significance	21	42126448	42126448	Human		name
598190930	CV3925513	single nucleotide variant	NM_001004416.3(UMODL1):c.3397G>T (p.Ala1133Ser)	not specified [RCV005288278]	uncertain significance	21	42127109	42127109	Human		name
8637524	CV92750	single nucleotide variant	NM_001004416.2(UMODL1):c.3032C>T (p.Ser1011Phe)	Malignant melanoma [RCV000072848]	not provided	21	42123035	42123035	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

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Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

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