Usp31 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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142 records found for search term Usp31

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598204004	CV3936620	single nucleotide variant	NM_020718.4(USP31):c.8A>G (p.Lys3Arg)	not specified [RCV005290623]	uncertain significance	16	23149263	23149263	Human		name
329398896	CV2471776	single nucleotide variant	NM_020718.4(USP31):c.16G>T (p.Ala6Ser)	not specified [RCV004280819]	uncertain significance	16	23149255	23149255	Human		name
156257000	CV2307846	single nucleotide variant	NM_020718.4(USP31):c.47G>A (p.Ser16Asn)	not specified [RCV004170308]	uncertain significance	16	23149224	23149224	Human		name
156292704	CV2321238	single nucleotide variant	NM_020718.4(USP31):c.62G>C (p.Arg21Pro)	not specified [RCV004175355]	uncertain significance	16	23149209	23149209	Human		name
407462660	CV3487533	single nucleotide variant	NM_020718.4(USP31):c.65C>T (p.Ser22Phe)	not specified [RCV004688036]	uncertain significance	16	23149206	23149206	Human		name
598275235	CV3936616	single nucleotide variant	NM_020718.4(USP31):c.35C>A (p.Pro12Gln)	not specified [RCV005304369]	uncertain significance	16	23149236	23149236	Human		name
156134964	CV2256800	single nucleotide variant	NM_020718.4(USP31):c.287C>G (p.Pro96Arg)	not specified [RCV004121023]	uncertain significance	16	23148984	23148984	Human		name
156229766	CV2267760	single nucleotide variant	NM_020718.4(USP31):c.163C>T (p.Pro55Ser)	not specified [RCV004134288]	uncertain significance	16	23149108	23149108	Human		name
156069829	CV2295764	single nucleotide variant	NM_020718.4(USP31):c.125G>A (p.Gly42Glu)	not specified [RCV004151692]	uncertain significance	16	23149146	23149146	Human		name
156252767	CV2311401	single nucleotide variant	NM_020718.4(USP31):c.284C>G (p.Pro95Arg)	not specified [RCV004168251]	uncertain significance	16	23148987	23148987	Human		name
401732676	CV2708934	single nucleotide variant	NM_020718.4(USP31):c.290G>T (p.Gly97Val)	not specified [RCV004309902]	uncertain significance	16	23148981	23148981	Human		name
401938581	CV2807731	single nucleotide variant	NM_020718.4(USP31):c.2991C>T (p.Ser997=)	not provided [RCV003417679]	likely benign	16	23069114	23069114	Human		name
401934401	CV2807732	single nucleotide variant	NM_020718.4(USP31):c.2442G>A (p.Ser814=)	not provided [RCV003411292]	likely benign	16	23072091	23072091	Human		name
598275231	CV3936610	single nucleotide variant	NM_020718.4(USP31):c.143C>G (p.Ala48Gly)	not specified [RCV005304365]	uncertain significance	16	23149128	23149128	Human		name
8635718	CV90941	single nucleotide variant	NM_020718.3(USP31):c.2523C>T (p.Val841=)	Malignant melanoma [RCV000071039]	not provided	16	23069582	23069582	Human		name
8635719	CV90942	single nucleotide variant	NM_020718.3(USP31):c.1302T>C (p.Pro434=)	Malignant melanoma [RCV000071040]	not provided	16	23090737	23090737	Human		name
156183478	CV2222392	single nucleotide variant	NM_020718.4(USP31):c.677A>G (p.Gln226Arg)	not specified [RCV004099255]	uncertain significance	16	23108140	23108140	Human		name
155984592	CV2247775	single nucleotide variant	NM_020718.4(USP31):c.854A>G (p.Gln285Arg)	not specified [RCV004121243]	uncertain significance	16	23106405	23106405	Human		name
156216975	CV2253822	single nucleotide variant	NM_020718.4(USP31):c.643T>G (p.Ser215Ala)	not specified [RCV004127518]	uncertain significance	16	23108174	23108174	Human		name
155957490	CV2304162	single nucleotide variant	NM_020718.4(USP31):c.316C>G (p.Pro106Ala)	not specified [RCV004170193]	uncertain significance	16	23148955	23148955	Human		name
156002046	CV2378882	single nucleotide variant	NM_020718.4(USP31):c.632A>C (p.Lys211Thr)	not specified [RCV004231316]	uncertain significance	16	23148639	23148639	Human		name
401766067	CV2683516	single nucleotide variant	NM_020718.4(USP31):c.610C>T (p.Pro204Ser)	not specified [RCV004288264]	uncertain significance	16	23148661	23148661	Human		name
401748689	CV2692710	single nucleotide variant	NM_020718.4(USP31):c.355T>A (p.Cys119Ser)	not specified [RCV004306262]	uncertain significance	16	23148916	23148916	Human		name
401756953	CV2692711	single nucleotide variant	NM_020718.4(USP31):c.538G>T (p.Ala180Ser)	not specified [RCV004306263]	uncertain significance	16	23148733	23148733	Human		name
401770515	CV2707259	single nucleotide variant	NM_020718.4(USP31):c.332C>G (p.Pro111Arg)	not specified [RCV004310879]	uncertain significance	16	23148939	23148939	Human		name
401734556	CV2709535	single nucleotide variant	NM_020718.4(USP31):c.484C>G (p.Arg162Gly)	not specified [RCV004318772]	uncertain significance	16	23148787	23148787	Human		name
401772663	CV2719717	single nucleotide variant	NM_020718.4(USP31):c.532C>T (p.Arg178Cys)	not specified [RCV004329157]	uncertain significance	16	23148739	23148739	Human		name
401893301	CV2755425	single nucleotide variant	NM_020718.4(USP31):c.513C>G (p.Asp171Glu)	not specified [RCV004337583]	uncertain significance	16	23148758	23148758	Human		name
405815098	CV3341875	single nucleotide variant	NM_020718.4(USP31):c.319T>C (p.Cys107Arg)	not specified [RCV004484761]	uncertain significance	16	23148952	23148952	Human		name
405663885	CV3341884	single nucleotide variant	NM_020718.4(USP31):c.383C>T (p.Ala128Val)	not specified [RCV004484770]	uncertain significance	16	23148888	23148888	Human		name
405815116	CV3341885	single nucleotide variant	NM_020718.4(USP31):c.539C>G (p.Ala180Gly)	not specified [RCV004484771]	uncertain significance	16	23148732	23148732	Human		name
405815118	CV3341886	single nucleotide variant	NM_020718.4(USP31):c.608C>T (p.Thr203Ile)	not specified [RCV004484772]	uncertain significance	16	23148663	23148663	Human		name
405815120	CV3341887	single nucleotide variant	NM_020718.4(USP31):c.665G>A (p.Arg222Gln)	not specified [RCV004484773]	uncertain significance	16	23108152	23108152	Human		name
405815121	CV3341888	single nucleotide variant	NM_020718.4(USP31):c.803G>A (p.Gly268Glu)	not specified [RCV004484774]	uncertain significance	16	23106456	23106456	Human		name
407455346	CV3487532	single nucleotide variant	NM_020718.4(USP31):c.362C>T (p.Ala121Val)	not specified [RCV004685526]	uncertain significance	16	23148909	23148909	Human		name
407455353	CV3487535	single nucleotide variant	NM_020718.4(USP31):c.795G>A (p.Met265Ile)	not specified [RCV004685528]	uncertain significance	16	23106464	23106464	Human		name
597723350	CV3626311	single nucleotide variant	NM_020718.4(USP31):c.599T>G (p.Leu200Arg)	not specified [RCV004888074]	uncertain significance	16	23148672	23148672	Human		name
597723366	CV3626312	single nucleotide variant	NM_020718.4(USP31):c.892C>G (p.Gln298Glu)	not specified [RCV004888075]	uncertain significance	16	23106274	23106274	Human		name
597798642	CV3626316	single nucleotide variant	NM_020718.4(USP31):c.811T>A (p.Phe271Ile)	not specified [RCV004879293]	uncertain significance	16	23106448	23106448	Human		name
597798644	CV3626319	single nucleotide variant	NM_020718.4(USP31):c.943C>T (p.Pro315Ser)	not specified [RCV004879294]	uncertain significance	16	23106223	23106223	Human		name
598275232	CV3936612	single nucleotide variant	NM_020718.4(USP31):c.353C>G (p.Ala118Gly)	not specified [RCV005304366]	uncertain significance	16	23148918	23148918	Human		name
598203983	CV3936617	single nucleotide variant	NM_020718.4(USP31):c.736C>T (p.His246Tyr)	not specified [RCV005290620]	uncertain significance	16	23108081	23108081	Human		name
8635720	CV90943	single nucleotide variant	NM_020718.3(USP31):c.937C>T (p.Pro313Ser)	Malignant melanoma [RCV000071041]	not provided	16	23106229	23106229	Human		name
156075877	CV2198129	single nucleotide variant	NM_020718.4(USP31):c.1198G>C (p.Glu400Gln)	not specified [RCV004079722]	uncertain significance	16	23102355	23102355	Human		name
156370903	CV2204372	single nucleotide variant	NM_020718.4(USP31):c.2072C>G (p.Pro691Arg)	not specified [RCV004079191]	uncertain significance	16	23080050	23080050	Human		name
156327211	CV2217226	single nucleotide variant	NM_020718.4(USP31):c.2856A>C (p.Glu952Asp)	not specified [RCV004087678]	uncertain significance	16	23069249	23069249	Human		name
156313803	CV2257064	single nucleotide variant	NM_020718.4(USP31):c.2200G>A (p.Gly734Ser)	not specified [RCV004123031]	uncertain significance	16	23073857	23073857	Human		name
156039732	CV2261235	single nucleotide variant	NM_020718.4(USP31):c.1261C>T (p.His421Tyr)	not specified [RCV004128110]	uncertain significance	16	23090778	23090778	Human		name
155906795	CV2279430	single nucleotide variant	NM_020718.4(USP31):c.2816G>A (p.Arg939Gln)	not specified [RCV004141971]	uncertain significance	16	23069289	23069289	Human		name
156280242	CV2338373	single nucleotide variant	NM_020718.4(USP31):c.1977G>T (p.Gln659His)	not specified [RCV004186422]	uncertain significance	16	23080145	23080145	Human		name
155976229	CV2338573	single nucleotide variant	NM_020718.4(USP31):c.2888T>C (p.Val963Ala)	not specified [RCV004182167]	uncertain significance	16	23069217	23069217	Human		name
156153235	CV2394947	single nucleotide variant	NM_020718.4(USP31):c.2585G>T (p.Cys862Phe)	not specified [RCV004234595]	uncertain significance	16	23069520	23069520	Human		name
329392976	CV2449417	single nucleotide variant	NM_020718.4(USP31):c.1547G>A (p.Arg516His)	not specified [RCV004266577]	uncertain significance	16	23087167	23087167	Human		name
329393021	CV2449447	single nucleotide variant	NM_020718.4(USP31):c.2425C>T (p.Arg809Cys)	not specified [RCV004268393]	uncertain significance	16	23072108	23072108	Human		name
329352167	CV2452155	single nucleotide variant	NM_020718.4(USP31):c.1262A>T (p.His421Leu)	not specified [RCV004278868]	uncertain significance	16	23090777	23090777	Human		name
329402441	CV2454262	single nucleotide variant	NM_020718.4(USP31):c.2815C>T (p.Arg939Trp)	not specified [RCV004265735]	uncertain significance	16	23069290	23069290	Human		name
401718985	CV2679374	single nucleotide variant	NM_020718.4(USP31):c.2312G>C (p.Trp771Ser)	not specified [RCV004285905]	uncertain significance	16	23073745	23073745	Human		name
401740624	CV2681478	single nucleotide variant	NM_020718.4(USP31):c.1546C>A (p.Arg516Ser)	not specified [RCV004292014]	uncertain significance	16	23087168	23087168	Human		name
401748841	CV2706085	single nucleotide variant	NM_020718.4(USP31):c.1465C>T (p.Leu489Phe)	not specified [RCV004314776]	uncertain significance	16	23087786	23087786	Human		name
401776205	CV2706925	single nucleotide variant	NM_020718.4(USP31):c.1036G>A (p.Val346Ile)	not specified [RCV004321536]	uncertain significance	16	23105494	23105494	Human		name
401783081	CV2716120	single nucleotide variant	NM_020718.4(USP31):c.1945C>T (p.Arg649Trp)	not specified [RCV004323362]	uncertain significance	16	23082443	23082443	Human		name
401784127	CV2721069	single nucleotide variant	NM_020718.4(USP31):c.2218G>A (p.Asp740Asn)	not specified [RCV004328329]	uncertain significance	16	23073839	23073839	Human		name
401778668	CV2735446	single nucleotide variant	NM_020718.4(USP31):c.1514C>T (p.Thr505Met)	not specified [RCV004331006]	uncertain significance	16	23087737	23087737	Human		name
401861522	CV2756327	single nucleotide variant	NM_020718.4(USP31):c.2576A>G (p.Asn859Ser)	not specified [RCV004342873]	uncertain significance	16	23069529	23069529	Human		name
401893566	CV2763667	single nucleotide variant	NM_020718.4(USP31):c.2491G>T (p.Gly831Cys)	not specified [RCV004343170]	uncertain significance	16	23069614	23069614	Human		name
401896233	CV2773859	single nucleotide variant	NM_020718.4(USP31):c.1090A>G (p.Ile364Val)	not specified [RCV004358300]	uncertain significance	16	23102463	23102463	Human		name
401892084	CV2777216	single nucleotide variant	NM_020718.4(USP31):c.2751C>G (p.Asn917Lys)	not specified [RCV004354249]	uncertain significance	16	23069354	23069354	Human		name
401896043	CV2777309	single nucleotide variant	NM_020718.4(USP31):c.2525A>G (p.Gln842Arg)	not specified [RCV004354324]	uncertain significance	16	23069580	23069580	Human		name
401869775	CV2782476	single nucleotide variant	NM_020718.4(USP31):c.2986G>C (p.Asp996His)	not specified [RCV004359527]	uncertain significance	16	23069119	23069119	Human		name
405815074	CV3341862	single nucleotide variant	NM_020718.4(USP31):c.1006A>C (p.Ile336Leu)	not specified [RCV004484748]	uncertain significance	16	23105524	23105524	Human		name
405815076	CV3341863	single nucleotide variant	NM_020718.4(USP31):c.1574A>G (p.Tyr525Cys)	not specified [RCV004484749]	uncertain significance	16	23087140	23087140	Human		name
405815078	CV3341864	single nucleotide variant	NM_020718.4(USP31):c.1829G>A (p.Arg610Gln)	not specified [RCV004484750]	uncertain significance	16	23084861	23084861	Human		name
405815080	CV3341865	single nucleotide variant	NM_020718.4(USP31):c.1840G>A (p.Asp614Asn)	not specified [RCV004484751]	uncertain significance	16	23082548	23082548	Human		name
405815083	CV3341867	single nucleotide variant	NM_020718.4(USP31):c.2528G>A (p.Arg843His)	not specified [RCV004484753]	uncertain significance	16	23069577	23069577	Human		name
405815085	CV3341868	single nucleotide variant	NM_020718.4(USP31):c.2688G>C (p.Leu896Phe)	not specified [RCV004484754]	uncertain significance	16	23069417	23069417	Human		name
405815087	CV3341869	single nucleotide variant	NM_020718.4(USP31):c.2740A>C (p.Ser914Arg)	not specified [RCV004484755]	uncertain significance	16	23069365	23069365	Human		name
405815089	CV3341870	single nucleotide variant	NM_020718.4(USP31):c.2752C>G (p.Leu918Val)	not specified [RCV004484756]	uncertain significance	16	23069353	23069353	Human		name
405815091	CV3341871	single nucleotide variant	NM_020718.4(USP31):c.2891A>G (p.Asp964Gly)	not specified [RCV004484757]	uncertain significance	16	23069214	23069214	Human		name
405815092	CV3341872	single nucleotide variant	NM_020718.4(USP31):c.2896C>G (p.Gln966Glu)	not specified [RCV004484758]	uncertain significance	16	23069209	23069209	Human		name
405815094	CV3341873	single nucleotide variant	NM_020718.4(USP31):c.2923C>T (p.Arg975Cys)	not specified [RCV004484759]	uncertain significance	16	23069182	23069182	Human		name
405815096	CV3341874	single nucleotide variant	NM_020718.4(USP31):c.2924G>A (p.Arg975His)	not specified [RCV004484760]	likely benign	16	23069181	23069181	Human		name
407462658	CV3487528	single nucleotide variant	NM_020718.4(USP31):c.2020C>T (p.His674Tyr)	not specified [RCV004688035]	uncertain significance	16	23080102	23080102	Human		name
407455338	CV3487529	single nucleotide variant	NM_020718.4(USP31):c.2861A>T (p.Asp954Val)	not specified [RCV004685523]	uncertain significance	16	23069244	23069244	Human		name
407455340	CV3487530	single nucleotide variant	NM_020718.4(USP31):c.1082C>G (p.Thr361Ser)	not specified [RCV004685524]	uncertain significance	16	23105448	23105448	Human		name
407455343	CV3487531	single nucleotide variant	NM_020718.4(USP31):c.2588T>C (p.Met863Thr)	not specified [RCV004685525]	uncertain significance	16	23069517	23069517	Human		name
407455349	CV3487534	single nucleotide variant	NM_020718.4(USP31):c.2882G>T (p.Ser961Ile)	not specified [RCV004685527]	uncertain significance	16	23069223	23069223	Human		name
597798627	CV3626306	single nucleotide variant	NM_020718.4(USP31):c.1963C>T (p.Arg655Cys)	not specified [RCV004879286]	uncertain significance	16	23080159	23080159	Human		name
597798629	CV3626307	single nucleotide variant	NM_020718.4(USP31):c.1561G>A (p.Val521Ile)	not specified [RCV004879287]	uncertain significance	16	23087153	23087153	Human		name
597798637	CV3626314	single nucleotide variant	NM_020718.4(USP31):c.2626C>T (p.Arg876Cys)	not specified [RCV004879291]	uncertain significance	16	23069479	23069479	Human		name
597798639	CV3626315	single nucleotide variant	NM_020718.4(USP31):c.2920G>A (p.Asp974Asn)	not specified [RCV004879292]	uncertain significance	16	23069185	23069185	Human		name
597723407	CV3626318	single nucleotide variant	NM_020718.4(USP31):c.1222C>A (p.Leu408Ile)	not specified [RCV004888078]	uncertain significance	16	23102331	23102331	Human		name
597723432	CV3626322	single nucleotide variant	NM_020718.4(USP31):c.2863A>G (p.Thr955Ala)	not specified [RCV004888080]	uncertain significance	16	23069242	23069242	Human		name
597723445	CV3626324	single nucleotide variant	NM_020718.4(USP31):c.1265T>G (p.Leu422Trp)	not specified [RCV004888081]	uncertain significance	16	23090774	23090774	Human		name
597723457	CV3626326	single nucleotide variant	NM_020718.4(USP31):c.1156A>G (p.Thr386Ala)	not specified [RCV004888082]	uncertain significance	16	23102397	23102397	Human		name
598275230	CV3936609	single nucleotide variant	NM_020718.4(USP31):c.1783A>G (p.Thr595Ala)	not specified [RCV005304364]	uncertain significance	16	23084907	23084907	Human		name
598203972	CV3936611	single nucleotide variant	NM_020718.4(USP31):c.1039G>T (p.Ala347Ser)	not specified [RCV005290618]	uncertain significance	16	23105491	23105491	Human		name
598275234	CV3936615	single nucleotide variant	NM_020718.4(USP31):c.1147G>A (p.Asp383Asn)	not specified [RCV005304368]	uncertain significance	16	23102406	23102406	Human		name
598203990	CV3936618	single nucleotide variant	NM_020718.4(USP31):c.2758A>G (p.Ser920Gly)	not specified [RCV005290621]	uncertain significance	16	23069347	23069347	Human		name
598275236	CV3936621	single nucleotide variant	NM_020718.4(USP31):c.1602G>T (p.Leu534Phe)	not specified [RCV005304370]	uncertain significance	16	23087112	23087112	Human		name
598275237	CV3936622	single nucleotide variant	NM_020718.4(USP31):c.1900C>T (p.Leu634Phe)	not specified [RCV005304371]	uncertain significance	16	23082488	23082488	Human		name
598275238	CV3936623	single nucleotide variant	NM_020718.4(USP31):c.2942G>A (p.Gly981Asp)	not specified [RCV005304372]	likely benign	16	23069163	23069163	Human		name
126909484	CV972471	single nucleotide variant	NM_020718.4(USP31):c.2533A>G (p.Ser845Gly)	Sensorineural hearing loss disorder [RCV001353212]	uncertain significance	16	23069572	23069572	Human	2	name
156246696	CV2228324	single nucleotide variant	NM_020718.4(USP31):c.3401C>T (p.Ser1134Leu)	not specified [RCV004098319]	uncertain significance	16	23068704	23068704	Human		name
155911933	CV2235461	single nucleotide variant	NM_020718.4(USP31):c.2999G>C (p.Ser1000Thr)	not specified [RCV004109509]	uncertain significance	16	23069106	23069106	Human		name
156276095	CV2255749	single nucleotide variant	NM_020718.4(USP31):c.3526C>T (p.Pro1176Ser)	not specified [RCV004120135]	uncertain significance	16	23068579	23068579	Human		name
156080460	CV2258259	single nucleotide variant	NM_020718.4(USP31):c.3176C>T (p.Ser1059Phe)	not specified [RCV004121629]	uncertain significance	16	23068929	23068929	Human		name
155904764	CV2276134	single nucleotide variant	NM_020718.4(USP31):c.3035C>T (p.Pro1012Leu)	not specified [RCV004141797]	uncertain significance	16	23069070	23069070	Human		name
156292259	CV2296784	single nucleotide variant	NM_020718.4(USP31):c.3718C>T (p.Arg1240Cys)	not specified [RCV004148680]	uncertain significance	16	23068387	23068387	Human		name
156046882	CV2304305	single nucleotide variant	NM_020718.4(USP31):c.3451G>A (p.Asp1151Asn)	not specified [RCV004164426]	uncertain significance	16	23068654	23068654	Human		name
155923116	CV2336784	single nucleotide variant	NM_020718.4(USP31):c.3952T>A (p.Ser1318Thr)	not specified [RCV004190407]	uncertain significance	16	23068153	23068153	Human		name
155969911	CV2338010	single nucleotide variant	NM_020718.4(USP31):c.3938C>T (p.Ser1313Phe)	not specified [RCV004186052]	uncertain significance	16	23068167	23068167	Human		name
155996622	CV2373091	single nucleotide variant	NM_020718.4(USP31):c.3514T>A (p.Ser1172Thr)	not specified [RCV004217786]	uncertain significance	16	23068591	23068591	Human		name
156059208	CV2396556	single nucleotide variant	NM_020718.4(USP31):c.3539G>A (p.Arg1180Gln)	not specified [RCV004242259]	uncertain significance	16	23068566	23068566	Human		name
329374013	CV2434668	single nucleotide variant	NM_020718.4(USP31):c.3535C>G (p.Pro1179Ala)	not specified [RCV004248387]	uncertain significance	16	23068570	23068570	Human		name
329379325	CV2443367	single nucleotide variant	NM_020718.4(USP31):c.3971C>T (p.Pro1324Leu)	not specified [RCV004260166]	uncertain significance	16	23068134	23068134	Human		name
401767687	CV2681744	single nucleotide variant	NM_020718.4(USP31):c.3614G>A (p.Arg1205His)	not specified [RCV004294285]	uncertain significance	16	23068491	23068491	Human		name
401734115	CV2713334	single nucleotide variant	NM_020718.4(USP31):c.3302C>G (p.Pro1101Arg)	not specified [RCV004318635]	uncertain significance	16	23068803	23068803	Human		name
401899088	CV2786043	single nucleotide variant	NM_020718.4(USP31):c.3164G>A (p.Ser1055Asn)	not specified [RCV004359867]	uncertain significance	16	23068941	23068941	Human		name
401934400	CV2807730	single nucleotide variant	NM_020718.4(USP31):c.4018A>G (p.Ser1340Gly)	not provided [RCV003411291]	likely benign	16	23068087	23068087	Human		name
405815100	CV3341876	single nucleotide variant	NM_020718.4(USP31):c.3202C>G (p.Leu1068Val)	not specified [RCV004484762]	likely benign	16	23068903	23068903	Human		name
405815101	CV3341877	single nucleotide variant	NM_020718.4(USP31):c.3286A>G (p.Lys1096Glu)	not specified [RCV004484763]	uncertain significance	16	23068819	23068819	Human		name
405815103	CV3341878	single nucleotide variant	NM_020718.4(USP31):c.3511A>G (p.Thr1171Ala)	not specified [RCV004484764]	uncertain significance	16	23068594	23068594	Human		name
405815105	CV3341879	single nucleotide variant	NM_020718.4(USP31):c.3586G>A (p.Val1196Met)	not specified [RCV004484765]	uncertain significance	16	23068519	23068519	Human		name
405815107	CV3341880	single nucleotide variant	NM_020718.4(USP31):c.3613C>T (p.Arg1205Cys)	not specified [RCV004484766]	uncertain significance	16	23068492	23068492	Human		name
405815108	CV3341881	single nucleotide variant	NM_020718.4(USP31):c.3715C>T (p.Arg1239Trp)	not specified [RCV004484767]	uncertain significance	16	23068390	23068390	Human		name
405815110	CV3341882	single nucleotide variant	NM_020718.4(USP31):c.3719G>A (p.Arg1240His)	not specified [RCV004484768]	uncertain significance	16	23068386	23068386	Human		name
405815112	CV3341883	single nucleotide variant	NM_020718.4(USP31):c.3722C>T (p.Ser1241Leu)	not specified [RCV004484769]	uncertain significance	16	23068383	23068383	Human		name
407462652	CV3487524	single nucleotide variant	NM_020718.4(USP31):c.3046G>C (p.Ala1016Pro)	not specified [RCV004688033]	uncertain significance	16	23069059	23069059	Human		name
407462655	CV3487526	single nucleotide variant	NM_020718.4(USP31):c.3577G>A (p.Gly1193Arg)	not specified [RCV004688034]	uncertain significance	16	23068528	23068528	Human		name
407455336	CV3487527	single nucleotide variant	NM_020718.4(USP31):c.3235T>A (p.Ser1079Thr)	not specified [RCV004685522]	uncertain significance	16	23068870	23068870	Human		name
597798631	CV3626308	single nucleotide variant	NM_020718.4(USP31):c.3214C>T (p.Arg1072Cys)	not specified [RCV004879288]	uncertain significance	16	23068891	23068891	Human		name
597798633	CV3626309	single nucleotide variant	NM_020718.4(USP31):c.4003A>G (p.Lys1335Glu)	not specified [RCV004879289]	uncertain significance	16	23068102	23068102	Human		name
597723381	CV3626313	single nucleotide variant	NM_020718.4(USP31):c.3926G>T (p.Arg1309Leu)	not specified [RCV004888076]	uncertain significance	16	23068179	23068179	Human		name
597723395	CV3626317	single nucleotide variant	NM_020718.4(USP31):c.3548A>G (p.Gln1183Arg)	not specified [RCV004888077]	uncertain significance	16	23068557	23068557	Human		name
597723421	CV3626320	single nucleotide variant	NM_020718.4(USP31):c.3833C>T (p.Pro1278Leu)	not specified [RCV004888079]	uncertain significance	16	23068272	23068272	Human		name
597798648	CV3626323	single nucleotide variant	NM_020718.4(USP31):c.3745T>A (p.Leu1249Met)	not specified [RCV004879296]	uncertain significance	16	23068360	23068360	Human		name
597798650	CV3626325	single nucleotide variant	NM_020718.4(USP31):c.3625A>G (p.Thr1209Ala)	not specified [RCV004879297]	likely benign	16	23068480	23068480	Human		name
598203966	CV3936607	single nucleotide variant	NM_020718.4(USP31):c.3799G>A (p.Gly1267Arg)	not specified [RCV005290617]	uncertain significance	16	23068306	23068306	Human		name
598275229	CV3936608	single nucleotide variant	NM_020718.4(USP31):c.3147G>T (p.Gln1049His)	not specified [RCV005304363]	uncertain significance	16	23068958	23068958	Human		name
598275233	CV3936613	single nucleotide variant	NM_020718.4(USP31):c.3932C>T (p.Ser1311Phe)	not specified [RCV005304367]	uncertain significance	16	23068173	23068173	Human		name
598203997	CV3936619	single nucleotide variant	NM_020718.4(USP31):c.3247G>A (p.Gly1083Ser)	not specified [RCV005290622]	uncertain significance	16	23068858	23068858	Human		name
8627778	CV82922	single nucleotide variant	NM_020718.3(USP31):c.3536C>T (p.Pro1179Leu)	Malignant melanoma [RCV000063002]	not provided	16	23068569	23068569	Human		name

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