Adamts20 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

197 records found for search term Adamts20

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8654002	CV130577	single nucleotide variant	NM_025003.3(ADAMTS20):c.453+4722G>A	Lung cancer [RCV000111064]	uncertain significance	12	43546187	43546187	Human		name
8634669	CV89889	single nucleotide variant	NM_025003.3(ADAMTS20):c.4284+1604G>A	Malignant melanoma [RCV000069986]	not provided	12	43423910	43423910	Human		name
401736296	CV2682662	single nucleotide variant	NM_025003.5(ADAMTS20):c.86G>A (p.Arg29Lys)	not specified [RCV004281644]	uncertain significance	12	43551836	43551836	Human		name
401932052	CV2806914	single nucleotide variant	NM_025003.5(ADAMTS20):c.354G>A (p.Glu118=)	not provided [RCV003391753]	likely benign	12	43551008	43551008	Human		name
156138796	CV2236774	single nucleotide variant	NM_025003.5(ADAMTS20):c.230G>T (p.Arg77Leu)	not specified [RCV004112544]	uncertain significance	12	43551132	43551132	Human		name
156329379	CV2342395	single nucleotide variant	NM_025003.5(ADAMTS20):c.220A>T (p.Met74Leu)	not specified [RCV004194008]	uncertain significance	12	43551142	43551142	Human		name
401733087	CV2712967	single nucleotide variant	NM_025003.5(ADAMTS20):c.276C>G (p.Asn92Lys)	not specified [RCV004314676]	uncertain significance	12	43551086	43551086	Human		name
401932051	CV2806913	single nucleotide variant	NM_025003.5(ADAMTS20):c.1300T>C (p.Leu434=)	not provided [RCV003391752]	likely benign	12	43466719	43466719	Human		name
405697879	CV3245764	single nucleotide variant	NM_025003.5(ADAMTS20):c.292T>C (p.Ser98Pro)	not specified [RCV004374688]	uncertain significance	12	43551070	43551070	Human		name
407456321	CV3419122	single nucleotide variant	NM_025003.5(ADAMTS20):c.284C>T (p.Ala95Val)	not specified [RCV004610682]	uncertain significance	12	43551078	43551078	Human		name
407456426	CV3419161	single nucleotide variant	NM_025003.5(ADAMTS20):c.104G>A (p.Arg35Lys)	not specified [RCV004610721]	uncertain significance	12	43551258	43551258	Human		name
407456454	CV3419171	single nucleotide variant	NM_025003.5(ADAMTS20):c.182T>A (p.Phe61Tyr)	not specified [RCV004610731]	uncertain significance	12	43551180	43551180	Human		name
597780570	CV3652820	single nucleotide variant	NM_025003.5(ADAMTS20):c.179A>G (p.His60Arg)	not specified [RCV004899544]	uncertain significance	12	43551183	43551183	Human		name
597789187	CV3652938	single nucleotide variant	NM_025003.5(ADAMTS20):c.267C>G (p.Phe89Leu)	not specified [RCV004901701]	uncertain significance	12	43551095	43551095	Human		name
598192988	CV3940259	single nucleotide variant	NM_025003.5(ADAMTS20):c.209C>T (p.Ala70Val)	not specified [RCV005312888]	uncertain significance	12	43551153	43551153	Human		name
15103581	CV725088	single nucleotide variant	NM_025003.5(ADAMTS20):c.2955G>A (p.Gly985=)	not provided [RCV000892706]	benign	12	43432445	43432445	Human		name
156140155	CV2202957	single nucleotide variant	NM_025003.5(ADAMTS20):c.776G>T (p.Arg259Ile)	not specified [RCV004069221]	uncertain significance	12	43502243	43502243	Human		name
156254652	CV2203263	single nucleotide variant	NM_025003.5(ADAMTS20):c.860T>C (p.Met287Thr)	not specified [RCV004071298]	uncertain significance	12	43502159	43502159	Human		name
155972686	CV2214352	single nucleotide variant	NM_025003.5(ADAMTS20):c.455C>T (p.Thr152Met)	not specified [RCV004086336]	likely benign	12	43532194	43532194	Human		name
156104981	CV2217471	single nucleotide variant	NM_025003.5(ADAMTS20):c.394C>G (p.Arg132Gly)	not specified [RCV004090018]	uncertain significance	12	43550968	43550968	Human		name
156232748	CV2245193	single nucleotide variant	NM_025003.5(ADAMTS20):c.332C>A (p.Thr111Asn)	not specified [RCV004106973]	uncertain significance	12	43551030	43551030	Human		name
156087205	CV2258969	single nucleotide variant	NM_025003.5(ADAMTS20):c.910C>A (p.His304Asn)	not specified [RCV004120244]	likely benign	12	43493211	43493211	Human		name
156210931	CV2259845	single nucleotide variant	NM_025003.5(ADAMTS20):c.548A>T (p.His183Leu)	not specified [RCV004117103]	uncertain significance	12	43532101	43532101	Human		name
156167959	CV2270525	single nucleotide variant	NM_025003.5(ADAMTS20):c.304G>A (p.Ala102Thr)	not specified [RCV004137482]	uncertain significance	12	43551058	43551058	Human		name
156257038	CV2277625	single nucleotide variant	NM_025003.5(ADAMTS20):c.632C>T (p.Thr211Ile)	not specified [RCV004147090]	uncertain significance	12	43502387	43502387	Human		name
156228327	CV2352899	single nucleotide variant	NM_025003.5(ADAMTS20):c.587A>C (p.Gln196Pro)	not specified [RCV004200946]	uncertain significance	12	43532062	43532062	Human		name
156223245	CV2355565	single nucleotide variant	NM_025003.5(ADAMTS20):c.598T>C (p.Tyr200His)	not specified [RCV004205410]	uncertain significance	12	43532051	43532051	Human		name
155918566	CV2362639	single nucleotide variant	NM_025003.5(ADAMTS20):c.757C>T (p.Arg253Cys)	not specified [RCV004215290]	uncertain significance	12	43502262	43502262	Human		name
329402896	CV2451521	single nucleotide variant	NM_025003.5(ADAMTS20):c.500T>A (p.Ile167Lys)	not specified [RCV004272178]	uncertain significance	12	43532149	43532149	Human		name
401884515	CV2761813	single nucleotide variant	NM_025003.5(ADAMTS20):c.868G>C (p.Val290Leu)	not specified [RCV004339458]	uncertain significance	12	43493253	43493253	Human		name
401932048	CV2806911	single nucleotide variant	NM_025003.5(ADAMTS20):c.4848C>T (p.Thr1616=)	not provided [RCV003391750]	likely benign	12	43377512	43377512	Human		name
401932050	CV2806912	single nucleotide variant	NM_025003.5(ADAMTS20):c.3093C>T (p.Ser1031=)	not provided [RCV003391751]	likely benign	12	43432307	43432307	Human		name
405698028	CV3245787	single nucleotide variant	NM_025003.5(ADAMTS20):c.335C>G (p.Pro112Arg)	not specified [RCV004374711]	uncertain significance	12	43551027	43551027	Human		name
405699567	CV3245861	single nucleotide variant	NM_025003.5(ADAMTS20):c.481G>A (p.Glu161Lys)	not specified [RCV004374785]	uncertain significance	12	43532168	43532168	Human		name
405698637	CV3245920	single nucleotide variant	NM_025003.5(ADAMTS20):c.657C>A (p.Ser219Arg)	not specified [RCV004374844]	likely benign	12	43502362	43502362	Human		name
405698650	CV3245922	single nucleotide variant	NM_025003.5(ADAMTS20):c.758G>T (p.Arg253Leu)	not specified [RCV004374846]	uncertain significance	12	43502261	43502261	Human		name
407456277	CV3419101	single nucleotide variant	NM_025003.5(ADAMTS20):c.787A>G (p.Ile263Val)	not specified [RCV004610661]	likely benign	12	43502232	43502232	Human		name
407456297	CV3419112	single nucleotide variant	NM_025003.5(ADAMTS20):c.865A>G (p.Ile289Val)	not specified [RCV004610672]	uncertain significance	12	43502154	43502154	Human		name
407456368	CV3419139	single nucleotide variant	NM_025003.5(ADAMTS20):c.781A>G (p.Ile261Val)	not specified [RCV004610699]	likely benign	12	43502238	43502238	Human		name
408367672	CV3511637	single nucleotide variant	NM_025003.5(ADAMTS20):c.5487A>G (p.Ala1829=)	ADAMTS20-related condition [RCV004759082]	likely benign	12	43369341	43369341	Human		name , trait
597780730	CV3652868	single nucleotide variant	NM_025003.5(ADAMTS20):c.563A>G (p.Gln188Arg)	not specified [RCV004899583]	uncertain significance	12	43532086	43532086	Human		name
597789198	CV3652946	single nucleotide variant	NM_025003.5(ADAMTS20):c.974A>G (p.Asp325Gly)	not specified [RCV004901704]	uncertain significance	12	43492607	43492607	Human		name
597789213	CV3652964	single nucleotide variant	NM_025003.5(ADAMTS20):c.717T>G (p.Asn239Lys)	not specified [RCV004901708]	uncertain significance	12	43502302	43502302	Human		name
8634668	CV89888	single nucleotide variant	NM_025003.3(ADAMTS20):c.4866G>A (p.Lys1622=)	Malignant melanoma [RCV000069985]	not provided	12	43377494	43377494	Human		name
8634674	CV89894	single nucleotide variant	NM_025003.3(ADAMTS20):c.684G>A (p.Met228Ile)	Malignant melanoma [RCV000069991]	not provided	12	43502335	43502335	Human		name
155918130	CV2195742	single nucleotide variant	NM_025003.5(ADAMTS20):c.2822C>A (p.Thr941Asn)	not specified [RCV004076098]	uncertain significance	12	43432710	43432710	Human		name
156192000	CV2206223	single nucleotide variant	NM_025003.5(ADAMTS20):c.1690C>G (p.Pro564Ala)	not specified [RCV004080656]	uncertain significance	12	43453977	43453977	Human		name
156333784	CV2220884	single nucleotide variant	NM_025003.5(ADAMTS20):c.1439G>C (p.Gly480Ala)	not specified [RCV004092310]	uncertain significance	12	43464661	43464661	Human		name
156213587	CV2257388	single nucleotide variant	NM_025003.5(ADAMTS20):c.2141G>C (p.Gly714Ala)	not specified [RCV004125475]	uncertain significance	12	43446651	43446651	Human		name
156241826	CV2283130	single nucleotide variant	NM_025003.5(ADAMTS20):c.2491C>G (p.Pro831Ala)	not specified [RCV004145818]	uncertain significance	12	43439724	43439724	Human		name
156083650	CV2289613	single nucleotide variant	NM_025003.5(ADAMTS20):c.2954G>A (p.Gly985Glu)	not specified [RCV004148537]	uncertain significance	12	43432446	43432446	Human		name
156279546	CV2297694	single nucleotide variant	NM_025003.5(ADAMTS20):c.1399C>A (p.Pro467Thr)	not specified [RCV004155375]	uncertain significance	12	43464701	43464701	Human		name
156275418	CV2316456	single nucleotide variant	NM_025003.5(ADAMTS20):c.1667A>G (p.Asn556Ser)	not specified [RCV004169940]	uncertain significance	12	43454000	43454000	Human		name
155973107	CV2320939	single nucleotide variant	NM_025003.5(ADAMTS20):c.1703G>A (p.Cys568Tyr)	not specified [RCV004172743]	uncertain significance	12	43453964	43453964	Human		name
156059873	CV2323049	single nucleotide variant	NM_025003.5(ADAMTS20):c.1291G>A (p.Ala431Thr)	not specified [RCV004185471]	uncertain significance	12	43466728	43466728	Human		name
155926474	CV2345198	single nucleotide variant	NM_025003.5(ADAMTS20):c.2665C>A (p.His889Asn)	not specified [RCV004195937]	uncertain significance	12	43434300	43434300	Human		name
156340803	CV2368321	single nucleotide variant	NM_025003.5(ADAMTS20):c.1040A>G (p.His347Arg)	not specified [RCV004219100]	uncertain significance	12	43492541	43492541	Human		name
156347580	CV2382930	single nucleotide variant	NM_025003.5(ADAMTS20):c.1508T>G (p.Ile503Arg)	not specified [RCV004217522]	uncertain significance	12	43464592	43464592	Human		name
156038886	CV2390259	single nucleotide variant	NM_025003.5(ADAMTS20):c.1849T>C (p.Phe617Leu)	not specified [RCV004240632]	uncertain significance	12	43452607	43452607	Human		name
155997059	CV2393266	single nucleotide variant	NM_025003.5(ADAMTS20):c.2500C>A (p.His834Asn)	not specified [RCV004228781]	uncertain significance	12	43439715	43439715	Human		name
155999116	CV2396366	single nucleotide variant	NM_025003.5(ADAMTS20):c.1522C>T (p.His508Tyr)	not specified [RCV004242089]	uncertain significance	12	43462987	43462987	Human		name
329384409	CV2435057	single nucleotide variant	NM_025003.5(ADAMTS20):c.1996T>A (p.Phe666Ile)	not specified [RCV004252707]	uncertain significance	12	43452357	43452357	Human		name
329366458	CV2445749	single nucleotide variant	NM_025003.5(ADAMTS20):c.1313T>C (p.Met438Thr)	not specified [RCV004259813]	likely benign	12	43466706	43466706	Human		name
329360462	CV2458763	single nucleotide variant	NM_025003.5(ADAMTS20):c.1916T>A (p.Val639Glu)	not specified [RCV004270197]	uncertain significance	12	43452540	43452540	Human		name
401742792	CV2677681	single nucleotide variant	NM_025003.5(ADAMTS20):c.2586G>A (p.Met862Ile)	not specified [RCV004291767]	uncertain significance	12	43439629	43439629	Human		name
401733572	CV2691342	single nucleotide variant	NM_025003.5(ADAMTS20):c.2242G>A (p.Asp748Asn)	not specified [RCV004303092]	uncertain significance	12	43443839	43443839	Human		name
401725671	CV2697514	single nucleotide variant	NM_025003.5(ADAMTS20):c.2248C>T (p.Arg750Cys)	not specified [RCV004297902]	uncertain significance	12	43443833	43443833	Human		name
401760509	CV2705957	single nucleotide variant	NM_025003.5(ADAMTS20):c.1831C>T (p.Pro611Ser)	not specified [RCV004320879]	uncertain significance	12	43452625	43452625	Human		name
401783680	CV2723836	single nucleotide variant	NM_025003.5(ADAMTS20):c.1714T>G (p.Cys572Gly)	not specified [RCV004325981]	uncertain significance	12	43453953	43453953	Human		name
401860207	CV2768515	single nucleotide variant	NM_025003.5(ADAMTS20):c.1880G>A (p.Gly627Asp)	not specified [RCV004344396]	uncertain significance	12	43452576	43452576	Human		name
401891413	CV2769163	single nucleotide variant	NM_025003.5(ADAMTS20):c.1460A>G (p.Lys487Arg)	not specified [RCV004349007]	uncertain significance	12	43464640	43464640	Human		name
401867184	CV2792627	single nucleotide variant	NM_025003.5(ADAMTS20):c.2690C>T (p.Thr897Ile)	not specified [RCV004363649]	uncertain significance	12	43434275	43434275	Human		name
405697450	CV3245688	single nucleotide variant	NM_025003.5(ADAMTS20):c.1649C>T (p.Thr550Met)	not specified [RCV004374612]	likely benign	12	43454018	43454018	Human		name
405697464	CV3245691	single nucleotide variant	NM_025003.5(ADAMTS20):c.1657C>T (p.Arg553Cys)	not specified [RCV004374615]	uncertain significance	12	43454010	43454010	Human		name
405697507	CV3245699	single nucleotide variant	NM_025003.5(ADAMTS20):c.1745G>T (p.Arg582Leu)	not specified [RCV004374623]	likely benign	12	43453922	43453922	Human		name
405697657	CV3245726	single nucleotide variant	NM_025003.5(ADAMTS20):c.2477G>T (p.Gly826Val)	not specified [RCV004374650]	uncertain significance	12	43439738	43439738	Human		name
405697740	CV3245740	single nucleotide variant	NM_025003.5(ADAMTS20):c.2651A>C (p.Asp884Ala)	not specified [RCV004374664]	uncertain significance	12	43434314	43434314	Human		name
405697785	CV3245748	single nucleotide variant	NM_025003.5(ADAMTS20):c.2761G>A (p.Gly921Ser)	not specified [RCV004374672]	uncertain significance	12	43432771	43432771	Human		name
405697839	CV3245757	single nucleotide variant	NM_025003.5(ADAMTS20):c.2811T>G (p.His937Gln)	not specified [RCV004374681]	uncertain significance	12	43432721	43432721	Human		name
405697896	CV3245767	single nucleotide variant	NM_025003.5(ADAMTS20):c.2981T>A (p.Met994Lys)	not specified [RCV004374691]	uncertain significance	12	43432419	43432419	Human		name
407456480	CV3419181	single nucleotide variant	NM_025003.5(ADAMTS20):c.1657C>G (p.Arg553Gly)	not specified [RCV004610741]	uncertain significance	12	43454010	43454010	Human		name
407456507	CV3419191	single nucleotide variant	NM_025003.5(ADAMTS20):c.2173G>T (p.Gly725Cys)	not specified [RCV004610751]	uncertain significance	12	43446619	43446619	Human		name
597780050	CV3652697	single nucleotide variant	NM_025003.5(ADAMTS20):c.2233A>G (p.Thr745Ala)	not specified [RCV004899421]	uncertain significance	12	43443848	43443848	Human		name
597780219	CV3652759	single nucleotide variant	NM_025003.5(ADAMTS20):c.2572G>A (p.Gly858Ser)	not specified [RCV004899483]	uncertain significance	12	43439643	43439643	Human		name
597780256	CV3652768	single nucleotide variant	NM_025003.5(ADAMTS20):c.1604G>A (p.Gly535Asp)	not specified [RCV004899492]	uncertain significance	12	43462905	43462905	Human		name
597780299	CV3652779	single nucleotide variant	NM_025003.5(ADAMTS20):c.1445G>A (p.Arg482Gln)	not specified [RCV004899503]	likely benign	12	43464655	43464655	Human		name
597780341	CV3652790	single nucleotide variant	NM_025003.5(ADAMTS20):c.1621C>T (p.Arg541Cys)	not specified [RCV004899514]	uncertain significance	12	43454046	43454046	Human		name
597780488	CV3652801	single nucleotide variant	NM_025003.5(ADAMTS20):c.2586G>T (p.Met862Ile)	not specified [RCV004899525]	uncertain significance	12	43439629	43439629	Human		name
597780496	CV3652803	single nucleotide variant	NM_025003.5(ADAMTS20):c.1297G>A (p.Ala433Thr)	not specified [RCV004899527]	likely benign	12	43466722	43466722	Human		name
597780578	CV3652825	single nucleotide variant	NM_025003.5(ADAMTS20):c.1998C>G (p.Phe666Leu)	not specified [RCV004899546]	uncertain significance	12	43452355	43452355	Human		name
597780582	CV3652829	single nucleotide variant	NM_025003.5(ADAMTS20):c.2002C>G (p.Leu668Val)	not specified [RCV004899547]	uncertain significance	12	43452351	43452351	Human		name
597780598	CV3652836	single nucleotide variant	NM_025003.5(ADAMTS20):c.2777C>T (p.Thr926Ile)	not specified [RCV004899551]	uncertain significance	12	43432755	43432755	Human		name
597780640	CV3652846	single nucleotide variant	NM_025003.5(ADAMTS20):c.2132G>T (p.Gly711Val)	not specified [RCV004899561]	uncertain significance	12	43446660	43446660	Human		name
597780838	CV3652896	single nucleotide variant	NM_025003.5(ADAMTS20):c.1633T>C (p.Cys545Arg)	not specified [RCV004899611]	uncertain significance	12	43454034	43454034	Human		name
597780923	CV3652918	single nucleotide variant	NM_025003.5(ADAMTS20):c.2264C>T (p.Ser755Phe)	not specified [RCV004899633]	uncertain significance	12	43443817	43443817	Human		name
597789163	CV3652927	single nucleotide variant	NM_025003.5(ADAMTS20):c.1310A>T (p.His437Leu)	not specified [RCV004901695]	uncertain significance	12	43466709	43466709	Human		name
597789194	CV3652944	single nucleotide variant	NM_025003.5(ADAMTS20):c.2224G>A (p.Ala742Thr)	not specified [RCV004901703]	likely benign	12	43443857	43443857	Human		name
597789209	CV3652959	single nucleotide variant	NM_025003.5(ADAMTS20):c.1603G>A (p.Gly535Ser)	not specified [RCV004901707]	uncertain significance	12	43462906	43462906	Human		name
597789221	CV3652974	single nucleotide variant	NM_025003.5(ADAMTS20):c.2664C>A (p.Asp888Glu)	not specified [RCV004901710]	uncertain significance	12	43434301	43434301	Human		name
598181134	CV3940132	single nucleotide variant	NM_025003.5(ADAMTS20):c.2386A>G (p.Ile796Val)	not specified [RCV005310802]	uncertain significance	12	43439974	43439974	Human		name
598181184	CV3940142	single nucleotide variant	NM_025003.5(ADAMTS20):c.2541G>A (p.Met847Ile)	not specified [RCV005310812]	uncertain significance	12	43439674	43439674	Human		name
598181319	CV3940172	single nucleotide variant	NM_025003.5(ADAMTS20):c.2507C>A (p.Ser836Tyr)	not specified [RCV005310840]	uncertain significance	12	43439708	43439708	Human		name
598181384	CV3940189	single nucleotide variant	NM_025003.5(ADAMTS20):c.2848G>C (p.Gly950Arg)	not specified [RCV005310854]	uncertain significance	12	43432684	43432684	Human		name
598181430	CV3940197	single nucleotide variant	NM_025003.5(ADAMTS20):c.1507A>G (p.Ile503Val)	not specified [RCV005310862]	uncertain significance	12	43464593	43464593	Human		name
598181521	CV3940217	single nucleotide variant	NM_025003.5(ADAMTS20):c.1258A>G (p.Lys420Glu)	not specified [RCV005310878]	uncertain significance	12	43466761	43466761	Human		name
598192883	CV3940233	single nucleotide variant	NM_025003.5(ADAMTS20):c.2404A>C (p.Asn802His)	not specified [RCV005312866]	uncertain significance	12	43439956	43439956	Human		name
598192977	CV3940255	single nucleotide variant	NM_025003.5(ADAMTS20):c.2843A>G (p.Tyr948Cys)	not specified [RCV005312885]	uncertain significance	12	43432689	43432689	Human		name
598193049	CV3940277	single nucleotide variant	NM_025003.5(ADAMTS20):c.2908T>C (p.Trp970Arg)	not specified [RCV005312902]	uncertain significance	12	43432624	43432624	Human		name
598193113	CV3940295	single nucleotide variant	NM_025003.5(ADAMTS20):c.2831T>C (p.Val944Ala)	not specified [RCV005312916]	uncertain significance	12	43432701	43432701	Human		name
598193160	CV3940304	single nucleotide variant	NM_025003.5(ADAMTS20):c.1351G>A (p.Val451Ile)	not specified [RCV005312924]	likely benign	12	43466668	43466668	Human		name
598193210	CV3940314	single nucleotide variant	NM_025003.5(ADAMTS20):c.1342C>T (p.Arg448Trp)	not specified [RCV005312933]	uncertain significance	12	43466677	43466677	Human		name
15172866	CV713521	single nucleotide variant	NM_025003.5(ADAMTS20):c.2745A>T (p.Glu915Asp)	not provided [RCV000972499]	benign	12	43432787	43432787	Human		name
8634672	CV89892	single nucleotide variant	NM_025003.3(ADAMTS20):c.1957C>T (p.Arg653Cys)	Malignant melanoma [RCV000069989]	not provided	12	43452396	43452396	Human		name
152042127	CV1669962	single nucleotide variant	NM_025003.5(ADAMTS20):c.4360G>T (p.Asp1454Tyr)	not provided [RCV002224864]	uncertain significance	12	43399158	43399158	Human		name
156318862	CV2200401	single nucleotide variant	NM_025003.5(ADAMTS20):c.5377G>C (p.Gly1793Arg)	not specified [RCV004076723]	uncertain significance	12	43375448	43375448	Human		name
156333503	CV2214610	single nucleotide variant	NM_025003.5(ADAMTS20):c.5030G>C (p.Arg1677Thr)	not specified [RCV004090444]	uncertain significance	12	43376619	43376619	Human		name
156063450	CV2228746	single nucleotide variant	NM_025003.5(ADAMTS20):c.4765A>C (p.Asn1589His)	not specified [RCV004093219]	uncertain significance	12	43383590	43383590	Human		name
156370103	CV2263475	single nucleotide variant	NM_025003.5(ADAMTS20):c.5484T>G (p.Asn1828Lys)	not specified [RCV004133717]	likely benign	12	43369344	43369344	Human		name
156229207	CV2267599	single nucleotide variant	NM_025003.5(ADAMTS20):c.4471T>C (p.Ser1491Pro)	not specified [RCV004134160]	uncertain significance	12	43383959	43383959	Human		name
156229856	CV2267778	single nucleotide variant	NM_025003.5(ADAMTS20):c.3937T>C (p.Trp1313Arg)	not specified [RCV004134305]	uncertain significance	12	43428249	43428249	Human		name
156301790	CV2307105	single nucleotide variant	NM_025003.5(ADAMTS20):c.3131G>A (p.Arg1044Gln)	not specified [RCV004159587]	uncertain significance	12	43431462	43431462	Human		name
156152891	CV2328482	single nucleotide variant	NM_025003.5(ADAMTS20):c.4213C>T (p.Pro1405Ser)	not specified [RCV004175861]	uncertain significance	12	43425585	43425585	Human		name
155971944	CV2335736	single nucleotide variant	NM_025003.5(ADAMTS20):c.4070G>A (p.Gly1357Glu)	not specified [RCV004193934]	uncertain significance	12	43427345	43427345	Human		name
156221149	CV2345117	single nucleotide variant	NM_025003.5(ADAMTS20):c.4591G>A (p.Val1531Met)	not specified [RCV004193389]	uncertain significance	12	43383839	43383839	Human		name
155907265	CV2354395	single nucleotide variant	NM_025003.5(ADAMTS20):c.3710A>G (p.Tyr1237Cys)	not specified [RCV004200348]	uncertain significance	12	43428476	43428476	Human		name
155909363	CV2359691	single nucleotide variant	NM_025003.5(ADAMTS20):c.5015T>C (p.Ile1672Thr)	not specified [RCV004210515]	uncertain significance	12	43376634	43376634	Human		name
155986880	CV2363734	single nucleotide variant	NM_025003.5(ADAMTS20):c.3523C>T (p.Arg1175Cys)	not specified [RCV004218722]	uncertain significance	12	43428766	43428766	Human		name
156211691	CV2378317	single nucleotide variant	NM_025003.5(ADAMTS20):c.5251C>G (p.Pro1751Ala)	not specified [RCV004226346]	uncertain significance	12	43376118	43376118	Human		name
155935865	CV2380124	single nucleotide variant	NM_025003.5(ADAMTS20):c.4837A>G (p.Thr1613Ala)	not specified [RCV004224501]	uncertain significance	12	43377523	43377523	Human		name
156388494	CV2380468	single nucleotide variant	NM_025003.5(ADAMTS20):c.3607G>T (p.Asp1203Tyr)	not specified [RCV004218065]	uncertain significance	12	43428682	43428682	Human		name
156183558	CV2382249	single nucleotide variant	NM_025003.5(ADAMTS20):c.5098G>T (p.Ala1700Ser)	not specified [RCV004228193]	uncertain significance	12	43376551	43376551	Human		name
156214110	CV2385895	single nucleotide variant	NM_025003.5(ADAMTS20):c.4219G>A (p.Val1407Ile)	not specified [RCV004226934]	uncertain significance	12	43425579	43425579	Human		name
155959611	CV2390558	single nucleotide variant	NM_025003.5(ADAMTS20):c.5443A>G (p.Lys1815Glu)	not specified [RCV004239090]	uncertain significance	12	43375382	43375382	Human		name
329355581	CV2434310	single nucleotide variant	NM_025003.5(ADAMTS20):c.4732C>G (p.Leu1578Val)	not specified [RCV004251982]	uncertain significance	12	43383623	43383623	Human		name
329401254	CV2442249	single nucleotide variant	NM_025003.5(ADAMTS20):c.4056G>T (p.Gln1352His)	not specified [RCV004264736]	uncertain significance	12	43427359	43427359	Human		name
329402275	CV2454117	single nucleotide variant	NM_025003.5(ADAMTS20):c.3149T>C (p.Leu1050Pro)	not specified [RCV004265614]	uncertain significance	12	43431444	43431444	Human		name
401773520	CV2695271	single nucleotide variant	NM_025003.5(ADAMTS20):c.3940G>A (p.Gly1314Arg)	not specified [RCV004303401]	uncertain significance	12	43428246	43428246	Human		name
401761008	CV2706180	single nucleotide variant	NM_025003.5(ADAMTS20):c.3485C>T (p.Thr1162Ile)	not specified [RCV004314859]	uncertain significance	12	43429621	43429621	Human		name
401777654	CV2718288	single nucleotide variant	NM_025003.5(ADAMTS20):c.3725A>T (p.Asp1242Val)	not specified [RCV004318129]	uncertain significance	12	43428461	43428461	Human		name
401777657	CV2718289	single nucleotide variant	NM_025003.5(ADAMTS20):c.3726T>G (p.Asp1242Glu)	not specified [RCV004318130]	uncertain significance	12	43428460	43428460	Human		name
401763180	CV2720224	single nucleotide variant	NM_025003.5(ADAMTS20):c.4120T>C (p.Cys1374Arg)	not specified [RCV004325561]	uncertain significance	12	43425678	43425678	Human		name
401865357	CV2754234	single nucleotide variant	NM_025003.5(ADAMTS20):c.4553G>A (p.Arg1518Gln)	not specified [RCV004334421]	uncertain significance	12	43383877	43383877	Human		name
401874765	CV2756045	single nucleotide variant	NM_025003.5(ADAMTS20):c.4222A>G (p.Ile1408Val)	not specified [RCV004338170]	likely benign	12	43425576	43425576	Human		name
401875711	CV2766974	single nucleotide variant	NM_025003.5(ADAMTS20):c.3427G>A (p.Ala1143Thr)	not specified [RCV004343358]	likely benign	12	43429679	43429679	Human		name
401864224	CV2767554	single nucleotide variant	NM_025003.5(ADAMTS20):c.4772T>C (p.Ile1591Thr)	not specified [RCV004343707]	uncertain significance	12	43383583	43383583	Human		name
401896887	CV2788908	single nucleotide variant	NM_025003.5(ADAMTS20):c.3073T>G (p.Trp1025Gly)	not specified [RCV004362945]	uncertain significance	12	43432327	43432327	Human		name
405697902	CV3245768	single nucleotide variant	NM_025003.5(ADAMTS20):c.2998C>T (p.Arg1000Cys)	not specified [RCV004374692]	uncertain significance	12	43432402	43432402	Human		name
405697987	CV3245780	single nucleotide variant	NM_025003.5(ADAMTS20):c.3230G>A (p.Cys1077Tyr)	not specified [RCV004374704]	uncertain significance	12	43431363	43431363	Human		name
405698050	CV3245791	single nucleotide variant	NM_025003.5(ADAMTS20):c.3475G>T (p.Gly1159Cys)	not specified [RCV004374715]	uncertain significance	12	43429631	43429631	Human		name
405698066	CV3245794	single nucleotide variant	NM_025003.5(ADAMTS20):c.3527A>G (p.Tyr1176Cys)	not specified [RCV004374718]	uncertain significance	12	43428762	43428762	Human		name
405698268	CV3245829	single nucleotide variant	NM_025003.5(ADAMTS20):c.4283C>T (p.Ser1428Leu)	not specified [RCV004374753]	uncertain significance	12	43425515	43425515	Human		name
405698284	CV3245832	single nucleotide variant	NM_025003.5(ADAMTS20):c.4334T>C (p.Ile1445Thr)	not specified [RCV004374756]	uncertain significance	12	43399184	43399184	Human		name
405699820	CV3245849	single nucleotide variant	NM_025003.5(ADAMTS20):c.4664G>A (p.Arg1555Gln)	not specified [RCV004374773]	likely benign	12	43383691	43383691	Human		name
405698364	CV3245871	single nucleotide variant	NM_025003.5(ADAMTS20):c.4915G>A (p.Val1639Met)	not specified [RCV004374795]	uncertain significance	12	43377445	43377445	Human		name
405698456	CV3245888	single nucleotide variant	NM_025003.5(ADAMTS20):c.5048C>A (p.Thr1683Asn)	not specified [RCV004374812]	uncertain significance	12	43376601	43376601	Human		name
405698484	CV3245893	single nucleotide variant	NM_025003.5(ADAMTS20):c.5126G>A (p.Cys1709Tyr)	not specified [RCV004374817]	uncertain significance	12	43376330	43376330	Human		name
405698536	CV3245902	single nucleotide variant	NM_025003.5(ADAMTS20):c.5306G>A (p.Gly1769Asp)	not specified [RCV004374826]	uncertain significance	12	43376063	43376063	Human		name
405698620	CV3245917	single nucleotide variant	NM_025003.5(ADAMTS20):c.5581T>G (p.Ser1861Ala)	not specified [RCV004374841]	uncertain significance	12	43356546	43356546	Human		name
407456203	CV3419073	single nucleotide variant	NM_025003.5(ADAMTS20):c.5365G>C (p.Glu1789Gln)	not specified [RCV004610633]	uncertain significance	12	43375460	43375460	Human		name
407456230	CV3419083	single nucleotide variant	NM_025003.5(ADAMTS20):c.4644G>C (p.Glu1548Asp)	not specified [RCV004610643]	uncertain significance	12	43383711	43383711	Human		name
407456253	CV3419092	single nucleotide variant	NM_025003.5(ADAMTS20):c.3112G>A (p.Gly1038Ser)	not specified [RCV004610652]	uncertain significance	12	43431481	43431481	Human		name
407456343	CV3419130	single nucleotide variant	NM_025003.5(ADAMTS20):c.5475A>G (p.Ile1825Met)	not specified [RCV004610690]	uncertain significance	12	43369353	43369353	Human		name
407456398	CV3419150	single nucleotide variant	NM_025003.5(ADAMTS20):c.4697T>C (p.Val1566Ala)	not specified [RCV004610710]	uncertain significance	12	43383658	43383658	Human		name
407456175	CV3422993	single nucleotide variant	NM_025003.5(ADAMTS20):c.5384T>C (p.Leu1795Ser)	not specified [RCV004610622]	uncertain significance	12	43375441	43375441	Human		name
408367579	CV3510175	single nucleotide variant	NM_025003.5(ADAMTS20):c.4090T>A (p.Tyr1364Asn)	ADAMTS20-related condition [RCV004759032]	likely benign	12	43427325	43427325	Human		name , trait
408367818	CV3515421	single nucleotide variant	NM_025003.5(ADAMTS20):c.5555A>G (p.Asn1852Ser)	ADAMTS20-related condition [RCV004759218]	likely benign	12	43356572	43356572	Human		name , trait
597779997	CV3652676	single nucleotide variant	NM_025003.5(ADAMTS20):c.4883G>A (p.Arg1628Gln)	not specified [RCV004899407]	likely benign	12	43377477	43377477	Human		name
597780026	CV3652684	single nucleotide variant	NM_025003.5(ADAMTS20):c.5096G>T (p.Gly1699Val)	not specified [RCV004899415]	uncertain significance	12	43376553	43376553	Human		name
597780100	CV3652708	single nucleotide variant	NM_025003.5(ADAMTS20):c.5630T>G (p.Ile1877Arg)	not specified [RCV004899432]	uncertain significance	12	43356497	43356497	Human		name
597780459	CV3652719	single nucleotide variant	NM_025003.5(ADAMTS20):c.4861A>G (p.Thr1621Ala)	not specified [RCV004899443]	uncertain significance	12	43377499	43377499	Human		name
597780413	CV3652730	single nucleotide variant	NM_025003.5(ADAMTS20):c.4708G>T (p.Val1570Phe)	not specified [RCV004899454]	likely benign	12	43383647	43383647	Human		name
597780380	CV3652738	single nucleotide variant	NM_025003.5(ADAMTS20):c.3607G>A (p.Asp1203Asn)	not specified [RCV004899462]	uncertain significance	12	43428682	43428682	Human		name
597780500	CV3652804	single nucleotide variant	NM_025003.5(ADAMTS20):c.3372T>G (p.Ser1124Arg)	not specified [RCV004899528]	uncertain significance	12	43430361	43430361	Human		name
597780536	CV3652812	single nucleotide variant	NM_025003.5(ADAMTS20):c.4925C>A (p.Ser1642Tyr)	not specified [RCV004899536]	uncertain significance	12	43377435	43377435	Human		name
597780574	CV3652821	single nucleotide variant	NM_025003.5(ADAMTS20):c.5342A>T (p.Asn1781Ile)	not specified [RCV004899545]	uncertain significance	12	43375483	43375483	Human		name
597780687	CV3652857	single nucleotide variant	NM_025003.5(ADAMTS20):c.4712A>G (p.Tyr1571Cys)	not specified [RCV004899572]	likely benign	12	43383643	43383643	Human		name
597780774	CV3652879	single nucleotide variant	NM_025003.5(ADAMTS20):c.4598A>G (p.His1533Arg)	not specified [RCV004899594]	uncertain significance	12	43383832	43383832	Human		name
597780800	CV3652886	single nucleotide variant	NM_025003.5(ADAMTS20):c.3796G>A (p.Ala1266Thr)	not specified [RCV004899601]	likely benign	12	43428390	43428390	Human		name
597780881	CV3652907	single nucleotide variant	NM_025003.5(ADAMTS20):c.5531G>A (p.Cys1844Tyr)	not specified [RCV004899622]	uncertain significance	12	43369297	43369297	Human		name
597789190	CV3652941	single nucleotide variant	NM_025003.5(ADAMTS20):c.5229T>G (p.Cys1743Trp)	not specified [RCV004901702]	uncertain significance	12	43376140	43376140	Human		name
597789201	CV3652951	single nucleotide variant	NM_025003.5(ADAMTS20):c.4787A>G (p.Asp1596Gly)	not specified [RCV004901705]	uncertain significance	12	43383568	43383568	Human		name
597789205	CV3652954	single nucleotide variant	NM_025003.5(ADAMTS20):c.5701A>G (p.Met1901Val)	not specified [RCV004901706]	uncertain significance	12	43354241	43354241	Human		name
597789217	CV3652968	single nucleotide variant	NM_025003.5(ADAMTS20):c.5052A>C (p.Lys1684Asn)	not specified [RCV004901709]	uncertain significance	12	43376597	43376597	Human		name
598181234	CV3940153	single nucleotide variant	NM_025003.5(ADAMTS20):c.4469G>T (p.Gly1490Val)	not specified [RCV005310822]	uncertain significance	12	43383961	43383961	Human		name
598181344	CV3940180	single nucleotide variant	NM_025003.5(ADAMTS20):c.5245G>C (p.Glu1749Gln)	not specified [RCV005310846]	uncertain significance	12	43376124	43376124	Human		name
598181476	CV3940207	single nucleotide variant	NM_025003.5(ADAMTS20):c.4273C>T (p.Pro1425Ser)	not specified [RCV005310869]	uncertain significance	12	43425525	43425525	Human		name
598181557	CV3940227	single nucleotide variant	NM_025003.5(ADAMTS20):c.5234A>G (p.Asp1745Gly)	not specified [RCV005310885]	likely benign	12	43376135	43376135	Human		name
598192908	CV3940239	single nucleotide variant	NM_025003.5(ADAMTS20):c.4318C>T (p.Arg1440Cys)	not specified [RCV005312871]	uncertain significance	12	43399200	43399200	Human		name
598192949	CV3940248	single nucleotide variant	NM_025003.5(ADAMTS20):c.4640G>C (p.Cys1547Ser)	not specified [RCV005312879]	uncertain significance	12	43383715	43383715	Human		name
598193013	CV3940268	single nucleotide variant	NM_025003.5(ADAMTS20):c.5389G>T (p.Ala1797Ser)	not specified [RCV005312894]	uncertain significance	12	43375436	43375436	Human		name
598193074	CV3940286	single nucleotide variant	NM_025003.5(ADAMTS20):c.3571T>C (p.Tyr1191His)	not specified [RCV005312908]	uncertain significance	12	43428718	43428718	Human		name
598240637	CV3940318	single nucleotide variant	NM_025003.5(ADAMTS20):c.3641G>C (p.Gly1214Ala)	not specified [RCV005321413]	uncertain significance	12	43428648	43428648	Human		name
598240647	CV3940321	single nucleotide variant	NM_025003.5(ADAMTS20):c.4271A>G (p.Glu1424Gly)	not specified [RCV005321415]	likely benign	12	43425527	43425527	Human		name
598240652	CV3940324	single nucleotide variant	NM_025003.5(ADAMTS20):c.4952G>C (p.Ser1651Thr)	not specified [RCV005321416]	uncertain significance	12	43377408	43377408	Human		name
8634670	CV89890	single nucleotide variant	NM_025003.3(ADAMTS20):c.3688C>T (p.Arg1230Ter)	Malignant melanoma [RCV000069987]	not provided	12	43428498	43428498	Human		name
8634671	CV89891	single nucleotide variant	NM_025003.3(ADAMTS20):c.3259C>T (p.Pro1087Ser)	Malignant melanoma [RCV000069988]	not provided	12	43431334	43431334	Human		name
8634673	CV89893	deletion	NM_025003.3(ADAMTS20):c.924delA (p.Lys309Asnfs)	Malignant melanoma [RCV000069990]	not provided	12	43493197	43493197	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)

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

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message