Adamts15 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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106 records found for search term Adamts15

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401860617	CV2752325	single nucleotide variant	NM_139055.4(ADAMTS15):c.1903-2A>G	Arthrogryposis, distal, type 12 [RCV003337698]	pathogenic	11	130471206	130471206	Human	1	name
8652725	CV129300	single nucleotide variant	NM_139055.2(ADAMTS15):c.1542+1799C>T	Lung cancer [RCV000109787]	uncertain significance	11	130464579	130464579	Human		name
596948176	CV3549256	single nucleotide variant	NM_139055.4(ADAMTS15):c.702C>T (p.His234=)	not provided [RCV004812076]	likely benign	11	130449675	130449675	Human		name
156017277	CV2266695	single nucleotide variant	NM_139055.4(ADAMTS15):c.244G>C (p.Glu82Gln)	not specified [RCV004131225]	uncertain significance	11	130449217	130449217	Human		name
156247940	CV2307069	single nucleotide variant	NM_139055.4(ADAMTS15):c.143C>A (p.Ser48Tyr)	not specified [RCV004159559]	uncertain significance	11	130449116	130449116	Human		name
155974102	CV2342507	single nucleotide variant	NM_139055.4(ADAMTS15):c.136G>A (p.Glu46Lys)	not specified [RCV004196605]	uncertain significance	11	130449109	130449109	Human		name
155906649	CV2357361	single nucleotide variant	NM_139055.4(ADAMTS15):c.178T>C (p.Phe60Leu)	not specified [RCV004200249]	uncertain significance	11	130449151	130449151	Human		name
401860616	CV2752324	single nucleotide variant	NM_139055.4(ADAMTS15):c.123C>G (p.Tyr41Ter)	Arthrogryposis, distal, type 12 [RCV003337697]	pathogenic	11	130449096	130449096	Human	1	name
401892057	CV2775909	single nucleotide variant	NM_139055.4(ADAMTS15):c.250C>G (p.Leu84Val)	not specified [RCV004344939]	uncertain significance	11	130449223	130449223	Human		name
401869702	CV2782452	single nucleotide variant	NM_139055.4(ADAMTS15):c.251T>A (p.Leu84Gln)	not specified [RCV004365178]	uncertain significance	11	130449224	130449224	Human		name
405688050	CV3305954	single nucleotide variant	NM_139055.4(ADAMTS15):c.200A>G (p.His67Arg)	not specified [RCV004444816]	uncertain significance	11	130449173	130449173	Human		name
598168104	CV3947215	single nucleotide variant	NM_139055.4(ADAMTS15):c.232G>A (p.Ala78Thr)	not specified [RCV005308182]	uncertain significance	11	130449205	130449205	Human		name
15193668	CV701666	single nucleotide variant	NM_139055.4(ADAMTS15):c.2505G>A (p.Pro835=)	not provided [RCV000955437]	benign	11	130473473	130473473	Human		name
15202381	CV701667	single nucleotide variant	NM_139055.4(ADAMTS15):c.2839C>T (p.Leu947=)	not provided [RCV000957898]	benign	11	130473807	130473807	Human		name
15158939	CV712725	single nucleotide variant	NM_139055.4(ADAMTS15):c.2160C>T (p.Ile720=)	not provided [RCV000969617]	benign	11	130473128	130473128	Human		name
15152666	CV724314	single nucleotide variant	NM_139055.4(ADAMTS15):c.2280C>T (p.Ser760=)	not provided [RCV000879853]	benign	11	130473248	130473248	Human		name
8626950	CV82094	single nucleotide variant	NM_139055.2(ADAMTS15):c.1560C>T (p.Ala520=)	Malignant melanoma [RCV000062173]	not provided	11	130469279	130469279	Human		name
8633942	CV89158	single nucleotide variant	NM_139055.2(ADAMTS15):c.2094C>T (p.Phe698=)	Malignant melanoma [RCV000069255]	not provided	11	130473062	130473062	Human		name
156203540	CV2300739	single nucleotide variant	NM_139055.4(ADAMTS15):c.571T>A (p.Tyr191Asn)	not specified [RCV004155674]	uncertain significance	11	130449544	130449544	Human		name
156051143	CV2336642	single nucleotide variant	NM_139055.4(ADAMTS15):c.769A>G (p.Ser257Gly)	not specified [RCV004196884]	uncertain significance	11	130449742	130449742	Human		name
156244499	CV2347155	single nucleotide variant	NM_139055.4(ADAMTS15):c.922G>A (p.Glu308Lys)	not specified [RCV004204631]	uncertain significance	11	130449895	130449895	Human		name
156135279	CV2379857	single nucleotide variant	NM_139055.4(ADAMTS15):c.958G>A (p.Asp320Asn)	not specified [RCV004219964]	uncertain significance	11	130461489	130461489	Human		name
329394554	CV2461409	single nucleotide variant	NM_139055.4(ADAMTS15):c.334G>C (p.Asp112His)	not specified [RCV004267561]	uncertain significance	11	130449307	130449307	Human		name
401727330	CV2684581	single nucleotide variant	NM_139055.4(ADAMTS15):c.647T>A (p.Ile216Asn)	not specified [RCV004293689]	uncertain significance	11	130449620	130449620	Human		name
401753704	CV2685031	single nucleotide variant	NM_139055.4(ADAMTS15):c.775C>T (p.Leu259Phe)	not specified [RCV004289614]	uncertain significance	11	130449748	130449748	Human		name
401885489	CV2783312	single nucleotide variant	NM_139055.4(ADAMTS15):c.547G>A (p.Ala183Thr)	not specified [RCV004363915]	uncertain significance	11	130449520	130449520	Human		name
401875378	CV2789035	single nucleotide variant	NM_139055.4(ADAMTS15):c.650C>G (p.Pro217Arg)	not specified [RCV004363340]	uncertain significance	11	130449623	130449623	Human		name
405783530	CV3306031	single nucleotide variant	NM_139055.4(ADAMTS15):c.653G>A (p.Arg218Gln)	not specified [RCV004437373]	uncertain significance	11	130449626	130449626	Human		name
597766879	CV3649550	single nucleotide variant	NM_139055.4(ADAMTS15):c.470T>C (p.Leu157Pro)	not specified [RCV004896247]	uncertain significance	11	130449443	130449443	Human		name
597766884	CV3649551	single nucleotide variant	NM_139055.4(ADAMTS15):c.413C>G (p.Pro138Arg)	not specified [RCV004896248]	uncertain significance	11	130449386	130449386	Human		name
597766889	CV3649553	single nucleotide variant	NM_139055.4(ADAMTS15):c.316G>A (p.Asp106Asn)	not specified [RCV004896249]	uncertain significance	11	130449289	130449289	Human		name
597766894	CV3649555	single nucleotide variant	NM_139055.4(ADAMTS15):c.850A>C (p.Asn284His)	not specified [RCV004896250]	uncertain significance	11	130449823	130449823	Human		name
15151919	CV712724	single nucleotide variant	NM_139055.4(ADAMTS15):c.703G>A (p.Gly235Ser)	not provided [RCV000968243]	benign	11	130449676	130449676	Human		name
155917011	CV2202148	single nucleotide variant	NM_139055.4(ADAMTS15):c.2075C>G (p.Pro692Arg)	not specified [RCV004078098]	uncertain significance	11	130471380	130471380	Human		name
156140604	CV2212202	single nucleotide variant	NM_139055.4(ADAMTS15):c.2777G>A (p.Arg926Gln)	not specified [RCV004089091]	uncertain significance	11	130473745	130473745	Human		name
156341131	CV2225765	single nucleotide variant	NM_139055.4(ADAMTS15):c.1120G>A (p.Val374Met)	not specified [RCV004103177]	uncertain significance	11	130462116	130462116	Human		name
156294063	CV2233605	single nucleotide variant	NM_139055.4(ADAMTS15):c.2285C>T (p.Thr762Met)	not specified [RCV004100075]	uncertain significance	11	130473253	130473253	Human		name
155921641	CV2240555	single nucleotide variant	NM_139055.4(ADAMTS15):c.1825G>A (p.Gly609Ser)	not specified [RCV004119210]	uncertain significance	11	130471024	130471024	Human		name
156069888	CV2295771	single nucleotide variant	NM_139055.4(ADAMTS15):c.1394G>A (p.Cys465Tyr)	not specified [RCV004151699]	uncertain significance	11	130462632	130462632	Human		name
155930308	CV2299851	single nucleotide variant	NM_139055.4(ADAMTS15):c.2111C>T (p.Ala704Val)	not specified [RCV004148997]	uncertain significance	11	130473079	130473079	Human		name
156045606	CV2308099	single nucleotide variant	NM_139055.4(ADAMTS15):c.1769A>G (p.Tyr590Cys)	not specified [RCV004170518]	uncertain significance	11	130470968	130470968	Human		name
156302725	CV2319700	single nucleotide variant	NM_139055.4(ADAMTS15):c.2770G>A (p.Gly924Arg)	not specified [RCV004187238]	uncertain significance	11	130473738	130473738	Human		name
155916906	CV2336233	single nucleotide variant	NM_139055.4(ADAMTS15):c.2599C>T (p.Arg867Trp)	not specified [RCV004191988]	uncertain significance	11	130473567	130473567	Human		name
155975795	CV2341597	single nucleotide variant	NM_139055.4(ADAMTS15):c.1963A>C (p.Ile655Leu)	not specified [RCV004188981]	uncertain significance	11	130471268	130471268	Human		name
155918905	CV2360101	single nucleotide variant	NM_139055.4(ADAMTS15):c.1448G>A (p.Arg483His)	not specified [RCV004215376]	uncertain significance	11	130462686	130462686	Human		name
156402402	CV2363971	single nucleotide variant	NM_139055.4(ADAMTS15):c.2666C>T (p.Ala889Val)	not specified [RCV004218938]	uncertain significance	11	130473634	130473634	Human		name
155934444	CV2372466	single nucleotide variant	NM_139055.4(ADAMTS15):c.2618G>A (p.Arg873His)	not specified [RCV004219265]	uncertain significance	11	130473586	130473586	Human		name
155994099	CV2377391	single nucleotide variant	NM_139055.4(ADAMTS15):c.2272C>T (p.Arg758Trp)	not specified [RCV004225568]	uncertain significance	11	130473240	130473240	Human		name
156157635	CV2378780	single nucleotide variant	NM_139055.4(ADAMTS15):c.2317C>T (p.Arg773Trp)	not specified [RCV004231231]	uncertain significance	11	130473285	130473285	Human		name
156133855	CV2383039	single nucleotide variant	NM_139055.4(ADAMTS15):c.2647C>T (p.Arg883Trp)	not specified [RCV004217620]	uncertain significance	11	130473615	130473615	Human		name
156190586	CV2385011	single nucleotide variant	NM_139055.4(ADAMTS15):c.1942G>A (p.Val648Ile)	not specified [RCV004228281]	uncertain significance	11	130471247	130471247	Human		name
155954748	CV2389813	single nucleotide variant	NM_139055.4(ADAMTS15):c.1970C>G (p.Ala657Gly)	not specified [RCV004236039]	uncertain significance	11	130471275	130471275	Human		name
155996421	CV2393179	single nucleotide variant	NM_139055.4(ADAMTS15):c.2695C>G (p.Leu899Val)	not specified [RCV004226654]	uncertain significance	11	130473663	130473663	Human		name
329375109	CV2444888	single nucleotide variant	NM_139055.4(ADAMTS15):c.2494G>A (p.Val832Met)	not specified [RCV004259124]	uncertain significance	11	130473462	130473462	Human		name
329382687	CV2445387	single nucleotide variant	NM_139055.4(ADAMTS15):c.1786C>T (p.Arg596Trp)	not specified [RCV004257462]	uncertain significance	11	130470985	130470985	Human		name
329386299	CV2455838	single nucleotide variant	NM_139055.4(ADAMTS15):c.1105A>G (p.Met369Val)	not specified [RCV004279123]	uncertain significance	11	130462101	130462101	Human		name
329370318	CV2461675	single nucleotide variant	NM_139055.4(ADAMTS15):c.2569A>G (p.Ser857Gly)	not specified [RCV004269837]	likely benign	11	130473537	130473537	Human		name
329353265	CV2469059	single nucleotide variant	NM_139055.4(ADAMTS15):c.1180C>G (p.Leu394Val)	not specified [RCV004274303]	uncertain significance	11	130462176	130462176	Human		name
401735946	CV2672783	single nucleotide variant	NM_139055.4(ADAMTS15):c.1991G>T (p.Gly664Val)	not specified [RCV004281566]	uncertain significance	11	130471296	130471296	Human		name
401742890	CV2677707	single nucleotide variant	NM_139055.4(ADAMTS15):c.1513G>A (p.Val505Met)	not specified [RCV004291789]	uncertain significance	11	130462751	130462751	Human		name
401778024	CV2704539	single nucleotide variant	NM_139055.4(ADAMTS15):c.2833T>G (p.Cys945Gly)	not specified [RCV004313273]	uncertain significance	11	130473801	130473801	Human		name
401718015	CV2714291	single nucleotide variant	NM_139055.4(ADAMTS15):c.1192G>T (p.Asp398Tyr)	not specified [RCV004315975]	uncertain significance	11	130462188	130462188	Human		name
401727147	CV2714834	single nucleotide variant	NM_139055.4(ADAMTS15):c.1520G>A (p.Arg507Lys)	not specified [RCV004320392]	uncertain significance	11	130462758	130462758	Human		name
401739325	CV2722106	single nucleotide variant	NM_139055.4(ADAMTS15):c.1934C>T (p.Ser645Phe)	not specified [RCV004328366]	uncertain significance	11	130471239	130471239	Human		name
401752117	CV2723125	single nucleotide variant	NM_139055.4(ADAMTS15):c.1213G>A (p.Ala405Thr)	not specified [RCV004329380]	uncertain significance	11	130462209	130462209	Human		name
401776194	CV2724612	single nucleotide variant	NM_139055.4(ADAMTS15):c.2504C>T (p.Pro835Leu)	not specified [RCV004331412]	uncertain significance	11	130473472	130473472	Human		name
401860620	CV2752326	single nucleotide variant	NM_139055.4(ADAMTS15):c.2281G>A (p.Gly761Ser)	Arthrogryposis, distal, type 12 [RCV003337699]	pathogenic	11	130473249	130473249	Human	1	name
401860621	CV2752327	single nucleotide variant	NM_139055.4(ADAMTS15):c.2715C>G (p.Cys905Trp)	Arthrogryposis, distal, type 12 [RCV003337700]	pathogenic	11	130473683	130473683	Human	1	name
401885435	CV2768162	single nucleotide variant	NM_139055.4(ADAMTS15):c.1634A>C (p.Asn545Thr)	not specified [RCV004350174]	uncertain significance	11	130469353	130469353	Human		name
401893883	CV2774165	single nucleotide variant	NM_139055.4(ADAMTS15):c.1984A>C (p.Asn662His)	not specified [RCV004345755]	uncertain significance	11	130471289	130471289	Human		name
401859069	CV2775073	single nucleotide variant	NM_139055.4(ADAMTS15):c.1937C>T (p.Thr646Ile)	not specified [RCV004346443]	uncertain significance	11	130471242	130471242	Human		name
401905768	CV2810026	single nucleotide variant	NM_139055.4(ADAMTS15):c.1606G>A (p.Val536Met)	not provided [RCV003396092]	likely benign	11	130469325	130469325	Human		name
405688128	CV3305913	single nucleotide variant	NM_139055.4(ADAMTS15):c.1744G>A (p.Glu582Lys)	not specified [RCV004444775]	uncertain significance	11	130470943	130470943	Human		name
405688065	CV3305957	single nucleotide variant	NM_139055.4(ADAMTS15):c.2026G>T (p.Gly676Trp)	not specified [RCV004444819]	uncertain significance	11	130471331	130471331	Human		name
405688258	CV3305970	single nucleotide variant	NM_139055.4(ADAMTS15):c.2309A>G (p.Gln770Arg)	not specified [RCV004444832]	uncertain significance	11	130473277	130473277	Human		name
405687671	CV3307166	single nucleotide variant	NM_139055.4(ADAMTS15):c.1175C>T (p.Pro392Leu)	not specified [RCV004444716]	uncertain significance	11	130462171	130462171	Human		name
405687734	CV3307179	single nucleotide variant	NM_139055.4(ADAMTS15):c.1360G>C (p.Val454Leu)	not specified [RCV004444729]	uncertain significance	11	130462598	130462598	Human		name
405687822	CV3307197	single nucleotide variant	NM_139055.4(ADAMTS15):c.1507G>A (p.Ala503Thr)	not specified [RCV004444747]	likely benign	11	130462745	130462745	Human		name
405687868	CV3307205	single nucleotide variant	NM_139055.4(ADAMTS15):c.1561A>G (p.Lys521Glu)	not specified [RCV004444755]	uncertain significance	11	130469280	130469280	Human		name
405687889	CV3307210	single nucleotide variant	NM_139055.4(ADAMTS15):c.1589G>A (p.Arg530His)	not specified [RCV004444760]	uncertain significance	11	130469308	130469308	Human		name
405688173	CV3307217	single nucleotide variant	NM_139055.4(ADAMTS15):c.1651G>A (p.Gly551Arg)	not specified [RCV004444767]	uncertain significance	11	130469370	130469370	Human		name
407502428	CV3425600	single nucleotide variant	NM_139055.4(ADAMTS15):c.2341G>A (p.Val781Met)	not specified [RCV004607671]	uncertain significance	11	130473309	130473309	Human		name
407502464	CV3425609	single nucleotide variant	NM_139055.4(ADAMTS15):c.1474A>G (p.Ser492Gly)	not specified [RCV004607680]	uncertain significance	11	130462712	130462712	Human		name
407450433	CV3425617	single nucleotide variant	NM_139055.4(ADAMTS15):c.2386T>C (p.Tyr796His)	not specified [RCV004607688]	uncertain significance	11	130473354	130473354	Human		name
407450511	CV3425627	single nucleotide variant	NM_139055.4(ADAMTS15):c.2441A>G (p.Asp814Gly)	not specified [RCV004607698]	uncertain significance	11	130473409	130473409	Human		name
407450538	CV3425638	single nucleotide variant	NM_139055.4(ADAMTS15):c.2442C>G (p.Asp814Glu)	not specified [RCV004607709]	uncertain significance	11	130473410	130473410	Human		name
407450570	CV3425647	single nucleotide variant	NM_139055.4(ADAMTS15):c.1412C>T (p.Thr471Ile)	not specified [RCV004607718]	uncertain significance	11	130462650	130462650	Human		name
407450592	CV3425657	single nucleotide variant	NM_139055.4(ADAMTS15):c.2332C>A (p.Pro778Thr)	not specified [RCV004607728]	uncertain significance	11	130473300	130473300	Human		name
597766577	CV3649479	single nucleotide variant	NM_139055.4(ADAMTS15):c.2509G>A (p.Asp837Asn)	not specified [RCV004896185]	uncertain significance	11	130473477	130473477	Human		name
597766594	CV3649489	single nucleotide variant	NM_139055.4(ADAMTS15):c.2630C>T (p.Ala877Val)	not specified [RCV004896188]	uncertain significance	11	130473598	130473598	Human		name
597766649	CV3649500	single nucleotide variant	NM_139055.4(ADAMTS15):c.2764G>A (p.Gly922Ser)	not specified [RCV004896199]	uncertain significance	11	130473732	130473732	Human		name
597766697	CV3649511	single nucleotide variant	NM_139055.4(ADAMTS15):c.1912G>A (p.Gly638Ser)	not specified [RCV004896209]	uncertain significance	11	130471217	130471217	Human		name
597766746	CV3649522	single nucleotide variant	NM_139055.4(ADAMTS15):c.1588C>T (p.Arg530Cys)	not specified [RCV004896220]	uncertain significance	11	130469307	130469307	Human		name
597766793	CV3649532	single nucleotide variant	NM_139055.4(ADAMTS15):c.2671G>A (p.Gly891Arg)	not specified [RCV004896230]	uncertain significance	11	130473639	130473639	Human		name
597766874	CV3649549	single nucleotide variant	NM_139055.4(ADAMTS15):c.2378G>A (p.Arg793Gln)	not specified [RCV004896246]	uncertain significance	11	130473346	130473346	Human		name
597766899	CV3649559	single nucleotide variant	NM_139055.4(ADAMTS15):c.1165A>G (p.Met389Val)	not specified [RCV004896251]	uncertain significance	11	130462161	130462161	Human		name
597766904	CV3649566	single nucleotide variant	NM_139055.4(ADAMTS15):c.2032G>A (p.Asp678Asn)	not specified [RCV004896252]	uncertain significance	11	130471337	130471337	Human		name
597766909	CV3649574	single nucleotide variant	NM_139055.4(ADAMTS15):c.2549C>G (p.Pro850Arg)	not specified [RCV004896253]	uncertain significance	11	130473517	130473517	Human		name
597766914	CV3649581	single nucleotide variant	NM_139055.4(ADAMTS15):c.1880A>G (p.Tyr627Cys)	not specified [RCV004896254]	uncertain significance	11	130471079	130471079	Human		name
598167949	CV3947177	single nucleotide variant	NM_139055.4(ADAMTS15):c.2038A>G (p.Lys680Glu)	not specified [RCV005308156]	uncertain significance	11	130471343	130471343	Human		name
598167979	CV3947187	single nucleotide variant	NM_139055.4(ADAMTS15):c.2231C>T (p.Ser744Leu)	not specified [RCV005308161]	uncertain significance	11	130473199	130473199	Human		name
598168026	CV3947197	single nucleotide variant	NM_139055.4(ADAMTS15):c.1667A>G (p.Glu556Gly)	not specified [RCV005308169]	uncertain significance	11	130469386	130469386	Human		name
598168066	CV3947206	single nucleotide variant	NM_139055.4(ADAMTS15):c.1559C>G (p.Ala520Gly)	not specified [RCV005308176]	uncertain significance	11	130469278	130469278	Human		name
598168149	CV3947223	single nucleotide variant	NM_139055.4(ADAMTS15):c.1076C>T (p.Thr359Ile)	not specified [RCV005308190]	uncertain significance	11	130461607	130461607	Human		name
598168156	CV3947224	single nucleotide variant	NM_139055.4(ADAMTS15):c.1838G>A (p.Arg613Gln)	not specified [RCV005308191]	uncertain significance	11	130471037	130471037	Human		name
8633941	CV89157	single nucleotide variant	NM_139055.2(ADAMTS15):c.1237G>A (p.Asp413Asn)	Malignant melanoma [RCV000069254]	not provided	11	130462233	130462233	Human		name

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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)

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