Adamtsl3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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263 records found for search term Adamtsl3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8584601	CV119175	single nucleotide variant	NM_207517.2(ADAMTSL3):c.*720A>G	Lung cancer [RCV000099695]	uncertain significance	15	84038526	84038526	Human		name
150487760	CV1283887	single nucleotide variant	NM_207517.3(ADAMTSL3):c.190-3T>C	not provided [RCV001716003]	benign	15	83773520	83773520	Human		name
15184567	CV778145	single nucleotide variant	NM_207517.3(ADAMTSL3):c.728-9C>G	not provided [RCV000952740]	benign	15	83858757	83858757	Human		name
150433014	CV1231637	single nucleotide variant	NM_207517.3(ADAMTSL3):c.803-78T>C	not provided [RCV001643299]	benign	15	83870724	83870724	Human		name
150461964	CV1234846	single nucleotide variant	NM_207517.3(ADAMTSL3):c.70-213G>A	not provided [RCV001649428]	benign	15	83704176	83704176	Human		name
150506758	CV1242292	single nucleotide variant	NM_207517.3(ADAMTSL3):c.364-34T>C	not provided [RCV001658647]	benign	15	83819777	83819777	Human		name
150510528	CV1242401	single nucleotide variant	NM_207517.3(ADAMTSL3):c.601-84C>A	not provided [RCV001660751]	benign	15	83838005	83838005	Human		name
150483727	CV1246999	single nucleotide variant	NM_207517.3(ADAMTSL3):c.-33-40G>A	not provided [RCV001673495]	benign	15	83655689	83655689	Human		name
150437313	CV1249849	single nucleotide variant	NM_207517.3(ADAMTSL3):c.363+58A>G	not provided [RCV001665763]	benign	15	83804753	83804753	Human		name
150500845	CV1283898	single nucleotide variant	NM_207517.3(ADAMTSL3):c.363+84G>A	not provided [RCV001718478]	benign	15	83804779	83804779	Human		name
15147635	CV779967	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4969+4C>G	not provided [RCV000967377]	benign	15	84036991	84036991	Human		name
15167484	CV779968	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4969+5G>A	not provided [RCV000971409]	likely benign	15	84036992	84036992	Human	1	name
15167484	CV779968	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4969+5G>A	not provided [RCV000971409]	likely benign	15	84036992	84036993	Human	1	name
150330855	CV1172780	single nucleotide variant	NM_207517.3(ADAMTSL3):c.318-239T>C	not provided [RCV001538325]	benign	15	83804411	83804411	Human		name
150336888	CV1172781	single nucleotide variant	NM_207517.3(ADAMTSL3):c.803-130G>T	not provided [RCV001541256]	benign	15	83870672	83870672	Human		name
150502997	CV1212375	single nucleotide variant	NM_207517.3(ADAMTSL3):c.728-195C>T	not provided [RCV001595249]	benign	15	83858571	83858571	Human		name
150464469	CV1214955	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1072+54G>C	not provided [RCV001613952]	benign	15	83885266	83885266	Human		name
150483953	CV1222390	single nucleotide variant	NM_207517.3(ADAMTSL3):c.727+108C>T	not provided [RCV001617393]	benign	15	83838323	83838323	Human		name
150486027	CV1223121	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1700+21A>G	not provided [RCV001617834]	benign	15	83899752	83899752	Human		name
150517380	CV1226830	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2311-25G>A	not provided [RCV001639924]	benign	15	83942878	83942878	Human		name
150509161	CV1229821	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1073-53A>C	not provided [RCV001636400]	benign	15	83890056	83890056	Human		name
150472848	CV1235127	single nucleotide variant	NM_207517.3(ADAMTSL3):c.961-230T>A	not provided [RCV001651496]	benign	15	83884871	83884871	Human		name
150486478	CV1251363	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4156+58C>T	not provided [RCV001674034]	benign	15	84014782	84014782	Human		name
150472222	CV1252209	single nucleotide variant	NM_207517.3(ADAMTSL3):c.961-295G>A	not provided [RCV001671410]	benign	15	83884806	83884806	Human		name
150461558	CV1253256	single nucleotide variant	NM_207517.3(ADAMTSL3):c.601-271A>G	not provided [RCV001669585]	benign	15	83837818	83837818	Human		name
150505464	CV1255479	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1468-66C>T	not provided [RCV001677926]	benign	15	83897792	83897792	Human		name
150444605	CV1258543	single nucleotide variant	NM_207517.3(ADAMTSL3):c.803-299T>C	not provided [RCV001679741]	benign	15	83870503	83870503	Human		name
150469155	CV1259610	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2490+22A>G	not provided [RCV001683911]	benign	15	83943104	83943104	Human		name
150447474	CV1261824	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2645-35G>T	not provided [RCV001680208]	benign	15	83982238	83982238	Human		name
150443220	CV1266363	single nucleotide variant	NM_207517.3(ADAMTSL3):c.189+110G>A	not provided [RCV001690799]	benign	15	83704618	83704618	Human		name
150443867	CV1266451	single nucleotide variant	NM_207517.3(ADAMTSL3):c.728-154A>G	not provided [RCV001690887]	benign	15	83858612	83858612	Human		name
150490493	CV1267623	single nucleotide variant	NM_207517.3(ADAMTSL3):c.803-275A>G	not provided [RCV001687647]	benign	15	83870527	83870527	Human		name
150459389	CV1268336	single nucleotide variant	NM_207517.3(ADAMTSL3):c.961-211G>A	not provided [RCV001693333]	benign	15	83884890	83884890	Human		name
150459101	CV1269747	deletion	NM_207517.3(ADAMTSL3):c.364-132del	not provided [RCV001693287]	benign	15	83819662	83819662	Human		name
150476095	CV1271285	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4755-99G>A	not provided [RCV001696108]	benign	15	84036674	84036674	Human		name
150497607	CV1271369	single nucleotide variant	NM_207517.3(ADAMTSL3):c.600+250C>G	not provided [RCV001689059]	benign	15	83820297	83820297	Human		name
150449466	CV1275674	duplication	NM_207517.3(ADAMTSL3):c.601-275dup	not provided [RCV001708129]	benign	15	83837802	83837803	Human		name
150451918	CV1276657	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1072+48A>G	not provided [RCV001708446]	benign	15	83885260	83885260	Human		name
150455041	CV1277117	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3844+77T>A	not provided [RCV001708909]	benign	15	83988895	83988895	Human		name
150465658	CV1277275	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3844+73T>A	not provided [RCV001710569]	benign	15	83988891	83988891	Human		name
150457757	CV1278671	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4156+51A>G	not provided [RCV001709287]	benign	15	84014775	84014775	Human		name
150458477	CV1278776	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1468-82G>C	not provided [RCV001709393]	benign	15	83897776	83897776	Human		name
150491272	CV1280267	single nucleotide variant	NM_207517.3(ADAMTSL3):c.803-134G>T	not provided [RCV001716615]	benign	15	83870668	83870668	Human		name
150512018	CV1284842	single nucleotide variant	NM_207517.3(ADAMTSL3):c.727+221G>A	not provided [RCV001721711]	benign	15	83838436	83838436	Human		name
243053538	CV2404639	single nucleotide variant	NM_207517.3(ADAMTSL3):c.318-243T>C	Lung adenocarcinoma [RCV003129666]	uncertain significance	15	83804407	83804407	Human	2	name
150333476	CV1169653	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1072+312C>A	not provided [RCV001537355]	benign	15	83885524	83885524	Human		name
150510560	CV1211767	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3973+290C>G	not provided [RCV001597663]	benign	15	83991504	83991504	Human		name
150465082	CV1215385	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4970-255C>T	not provided [RCV001614084]	benign	15	84037445	84037445	Human		name
150465899	CV1218098	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1073-208A>G	not provided [RCV001614224]	benign	15	83889901	83889901	Human		name
150468938	CV1218990	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3844+150G>A	not provided [RCV001614742]	benign	15	83988968	83988968	Human		name
150486531	CV1225756	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3974-203T>C	not provided [RCV001617917]	benign	15	84014339	84014339	Human		name
150517275	CV1226723	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2117+193C>T	not provided [RCV001639817]	benign	15	83924226	83924226	Human	2	name
150516988	CV1227427	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2491-260G>A	not provided [RCV001639528]	benign	15	83970224	83970224	Human		name
150511687	CV1229524	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4274-201G>A	not provided [RCV001637453]	benign	15	84021209	84021209	Human		name
150433881	CV1230649	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1468-166T>C	not provided [RCV001643595]	benign	15	83897692	83897692	Human		name
150460609	CV1234664	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1073-185A>G	not provided [RCV001649246]	benign	15	83889924	83889924	Human		name
150467099	CV1240520	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1262+251G>A	not provided [RCV001650281]	benign	15	83891630	83891630	Human		name
150464863	CV1241391	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1467+239C>T	not provided [RCV001649902]	benign	15	83893127	83893127	Human	8	name
150469785	CV1247879	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4755-120T>C	not provided [RCV001670915]	benign	15	84036653	84036653	Human		name
150437850	CV1249940	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1073-160T>C	not provided [RCV001665854]	benign	15	83889949	83889949	Human		name
150472935	CV1252325	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1616-241T>A	not provided [RCV001671527]	benign	15	83899406	83899406	Human	1	name
150502940	CV1254658	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1072+153A>G	not provided [RCV001677360]	benign	15	83885365	83885365	Human		name
150502150	CV1255220	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1987+174G>T	not provided [RCV001677139]	benign	15	83913552	83913552	Human		name
150440653	CV1265434	deletion	NM_207517.3(ADAMTSL3):c.1072+241del	not provided [RCV001679137]	benign	15	83885442	83885442	Human		name
150457985	CV1269569	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1701-239G>A	not provided [RCV001693109]	benign	15	83912853	83912853	Human		name
150464671	CV1276448	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1988-294T>A	not provided [RCV001710394]	benign	15	83923610	83923610	Human		name
150452044	CV1276675	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4157-256C>A	not provided [RCV001708464]	benign	15	84016127	84016127	Human		name
150465812	CV1277300	deletion	NM_207517.3(ADAMTSL3):c.1616-226del	not provided [RCV001710595]	benign	15	83899421	83899421	Human		name
150476101	CV1279190	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1072+237A>C	not provided [RCV001713935]	benign	15	83885449	83885449	Human		name
150500831	CV1283895	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1072+312C>T	not provided [RCV001718475]	benign	15	83885524	83885524	Human		name
150512029	CV1284845	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1468-217G>A	not provided [RCV001721714]	benign	15	83897641	83897641	Human		name
243053668	CV2404614	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2490+210C>G	Squamous cell carcinoma [RCV003129641]	uncertain significance	15	83943292	83943292	Human	2	name
243053669	CV2404615	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2490+207A>C	Squamous cell carcinoma [RCV003129642]	uncertain significance	15	83943289	83943289	Human	2	name
243053695	CV2404621	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1700+350A>T	Squamous cell carcinoma [RCV003129648]	uncertain significance	15	83900081	83900081	Human	2	name
156107003	CV2355291	single nucleotide variant	NM_207517.3(ADAMTSL3):c.14C>T (p.Thr5Met)	not specified [RCV004203142]	uncertain significance	15	83655775	83655775	Human		name
405665990	CV3239411	single nucleotide variant	NM_207517.3(ADAMTSL3):c.13A>T (p.Thr5Ser)	not specified [RCV004367655]	uncertain significance	15	83655774	83655774	Human		name
405666341	CV3239480	single nucleotide variant	NM_207517.3(ADAMTSL3):c.27G>T (p.Trp9Cys)	not specified [RCV004367724]	uncertain significance	15	83655788	83655788	Human		name
8627714	CV82858	single nucleotide variant	NM_207517.2(ADAMTSL3):c.102C>T (p.Phe34=)	Malignant melanoma [RCV000062938]	not provided	15	83704421	83704421	Human		name
150514231	CV1210925	insertion	NM_207517.3(ADAMTSL3):c.189+59_189+60insAG	not provided [RCV001598968]	benign	15	83704567	83704568	Human		name
156256397	CV2321979	single nucleotide variant	NM_207517.3(ADAMTSL3):c.68A>T (p.Gln23Leu)	not specified [RCV004173739]	uncertain significance	15	83655829	83655829	Human		name
401772020	CV2689712	single nucleotide variant	NM_207517.3(ADAMTSL3):c.58C>T (p.Pro20Ser)	not specified [RCV004297629]	uncertain significance	15	83655819	83655819	Human		name
597770878	CV3650020	single nucleotide variant	NM_207517.3(ADAMTSL3):c.65C>T (p.Pro22Leu)	not specified [RCV004897011]	likely benign	15	83655826	83655826	Human		name
15151984	CV739830	single nucleotide variant	NM_207517.3(ADAMTSL3):c.86C>A (p.Ser29Tyr)	not provided [RCV000901471]	likely benign	15	83704405	83704405	Human		name
150515611	CV1216266	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1761T>C (p.Arg587=)	not provided [RCV001608457]	benign	15	83913152	83913152	Human		name
150485500	CV1223009	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2805C>A (p.Pro935=)	not provided [RCV001617721]	benign	15	83982433	83982433	Human	3	name
150460842	CV1231399	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1746G>A (p.Pro582=)	not provided [RCV001640964]	benign	15	83913137	83913137	Human		name
150450113	CV1273725	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2910T>C (p.His970=)	not provided [RCV001691825]	benign	15	83982538	83982538	Human		name
156166821	CV2270442	single nucleotide variant	NM_207517.3(ADAMTSL3):c.212A>G (p.Asp71Gly)	not specified [RCV004137411]	uncertain significance	15	83773545	83773545	Human		name
407471472	CV3425926	single nucleotide variant	NM_207517.3(ADAMTSL3):c.170C>T (p.Thr57Ile)	not specified [RCV004615702]	uncertain significance	15	83704489	83704489	Human		name
407450931	CV3425962	single nucleotide variant	NM_207517.3(ADAMTSL3):c.200A>G (p.Asn67Ser)	not specified [RCV004607865]	uncertain significance	15	83773533	83773533	Human		name
597770731	CV3653412	single nucleotide variant	NM_207517.3(ADAMTSL3):c.173A>T (p.Tyr58Phe)	not specified [RCV004896979]	uncertain significance	15	83704492	83704492	Human		name
598242182	CV3944136	single nucleotide variant	NM_207517.3(ADAMTSL3):c.268A>G (p.Thr90Ala)	not specified [RCV005321685]	uncertain significance	15	83773601	83773601	Human		name
598241966	CV3947966	single nucleotide variant	NM_207517.3(ADAMTSL3):c.158A>G (p.Glu53Gly)	not specified [RCV005321643]	uncertain significance	15	83704477	83704477	Human		name
598209914	CV3947984	single nucleotide variant	NM_207517.3(ADAMTSL3):c.128A>G (p.Gln43Arg)	not specified [RCV005315778]	uncertain significance	15	83704447	83704447	Human		name
15193876	CV703378	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2622T>C (p.Ser874=)	not provided [RCV000955494]	benign	15	83970615	83970615	Human		name
15147627	CV714655	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2343C>T (p.Asn781=)	not provided [RCV000967376]	benign	15	83942935	83942935	Human		name
150466406	CV1218184	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3351G>A (p.Ala1117=)	not provided [RCV001614310]	benign	15	83982979	83982979	Human		name
150455057	CV1220401	deletion	NM_207517.3(ADAMTSL3):c.1212-311_1212-307del	not provided [RCV001612494]	benign	15	83891016	83891020	Human		name
150514622	CV1228577	single nucleotide variant	NM_207517.3(ADAMTSL3):c.868C>G (p.Leu290Val)	not provided [RCV001638565]	benign	15	83870867	83870867	Human		name
150430895	CV1231086	insertion	NM_207517.3(ADAMTSL3):c.3844+78_3844+79insAT	not provided [RCV001641635]	benign	15	83988895	83988896	Human		name
150435793	CV1233960	single nucleotide variant	NM_207517.3(ADAMTSL3):c.437A>G (p.His146Arg)	not provided [RCV001644087]	benign	15	83819884	83819884	Human		name
150506231	CV1242163	deletion	NM_207517.3(ADAMTSL3):c.1616-228_1616-227del	not provided [RCV001658516]	benign	15	83899419	83899420	Human		name
155922153	CV2218753	single nucleotide variant	NM_207517.3(ADAMTSL3):c.632A>G (p.Asn211Ser)	not specified [RCV004085006]	likely benign	15	83838120	83838120	Human		name
155976781	CV2246078	single nucleotide variant	NM_207517.3(ADAMTSL3):c.688G>T (p.Val230Leu)	not specified [RCV004113986]	uncertain significance	15	83838176	83838176	Human		name
155946015	CV2265944	single nucleotide variant	NM_207517.3(ADAMTSL3):c.922A>G (p.Lys308Glu)	not specified [RCV004126788]	uncertain significance	15	83870921	83870921	Human		name
156362792	CV2330375	single nucleotide variant	NM_207517.3(ADAMTSL3):c.380C>T (p.Ala127Val)	not specified [RCV004180950]	uncertain significance	15	83819827	83819827	Human		name
155924171	CV2352019	single nucleotide variant	NM_207517.3(ADAMTSL3):c.806T>C (p.Ile269Thr)	not specified [RCV004191118]	uncertain significance	15	83870805	83870805	Human		name
329374161	CV2443750	single nucleotide variant	NM_207517.3(ADAMTSL3):c.667G>A (p.Asp223Asn)	not specified [RCV004256049]	uncertain significance	15	83838155	83838155	Human		name
329360105	CV2446568	single nucleotide variant	NM_207517.3(ADAMTSL3):c.563C>T (p.Thr188Met)	not specified [RCV004251461]	uncertain significance	15	83820010	83820010	Human		name
329387622	CV2446729	single nucleotide variant	NM_207517.3(ADAMTSL3):c.764G>A (p.Arg255Gln)	not specified [RCV004253770]	uncertain significance	15	83858802	83858802	Human		name
401720390	CV2673306	single nucleotide variant	NM_207517.3(ADAMTSL3):c.617G>C (p.Arg206Pro)	not specified [RCV004288294]	uncertain significance	15	83838105	83838105	Human		name
401916452	CV2814428	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4878C>T (p.His1626=)	not provided [RCV003400992]	likely benign	15	84036896	84036896	Human		name
405666588	CV3239527	single nucleotide variant	NM_207517.3(ADAMTSL3):c.378T>A (p.Asp126Glu)	not specified [RCV004367771]	uncertain significance	15	83819825	83819825	Human		name
405666885	CV3239587	single nucleotide variant	NM_207517.3(ADAMTSL3):c.458G>A (p.Arg153Gln)	not specified [RCV004367831]	uncertain significance	15	83819905	83819905	Human		name
407471203	CV3425862	single nucleotide variant	NM_207517.3(ADAMTSL3):c.479C>T (p.Pro160Leu)	not specified [RCV004615638]	uncertain significance	15	83819926	83819926	Human		name
407471300	CV3425883	single nucleotide variant	NM_207517.3(ADAMTSL3):c.617G>A (p.Arg206Gln)	not specified [RCV004615659]	uncertain significance	15	83838105	83838105	Human		name
407450912	CV3425952	single nucleotide variant	NM_207517.3(ADAMTSL3):c.920T>A (p.Phe307Tyr)	not specified [RCV004607855]	uncertain significance	15	83870919	83870919	Human		name
407450989	CV3425983	single nucleotide variant	NM_207517.3(ADAMTSL3):c.803T>A (p.Phe268Tyr)	not specified [RCV004607886]	uncertain significance	15	83870802	83870802	Human		name
597770998	CV3650053	single nucleotide variant	NM_207517.3(ADAMTSL3):c.616C>G (p.Arg206Gly)	not specified [RCV004897037]	uncertain significance	15	83838104	83838104	Human		name
597770515	CV3653356	single nucleotide variant	NM_207517.3(ADAMTSL3):c.469C>A (p.Pro157Thr)	not specified [RCV004896931]	uncertain significance	15	83819916	83819916	Human		name
597770526	CV3653360	single nucleotide variant	NM_207517.3(ADAMTSL3):c.616C>T (p.Arg206Trp)	not specified [RCV004896933]	uncertain significance	15	83838104	83838104	Human		name
597770692	CV3653403	single nucleotide variant	NM_207517.3(ADAMTSL3):c.491A>C (p.Lys164Thr)	not specified [RCV004896970]	uncertain significance	15	83819938	83819938	Human		name
597770799	CV3653440	single nucleotide variant	NM_207517.3(ADAMTSL3):c.613G>A (p.Asp205Asn)	not specified [RCV004896994]	uncertain significance	15	83838101	83838101	Human		name
598210299	CV3944107	single nucleotide variant	NM_207517.3(ADAMTSL3):c.565G>A (p.Asp189Asn)	not specified [RCV005315834]	uncertain significance	15	83820012	83820012	Human		name
598209858	CV3947974	single nucleotide variant	NM_207517.3(ADAMTSL3):c.834A>C (p.Lys278Asn)	not specified [RCV005315770]	uncertain significance	15	83870833	83870833	Human		name
15189818	CV703379	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3486G>A (p.Ser1162=)	not provided [RCV000954292]	benign	15	83983114	83983114	Human		name
15140200	CV785044	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4977C>T (p.Cys1659=)	not provided [RCV000982775]	likely benign	15	84037707	84037707	Human		name
150513941	CV1210778	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2137G>C (p.Gly713Arg)	not provided [RCV001598819]	benign	15	83942615	83942615	Human		name
150484255	CV1222452	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2605C>T (p.Leu869Phe)	not provided [RCV001617455]	benign	15	83970598	83970598	Human		name
150438830	CV1264880	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1981G>T (p.Val661Leu)	not provided [RCV001678873]	benign	15	83913372	83913372	Human	3	name
156169048	CV2197748	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1011G>C (p.Gln337His)	not specified [RCV004074948]	uncertain significance	15	83885151	83885151	Human		name
156070043	CV2203919	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2110C>T (p.Pro704Ser)	not specified [RCV004069969]	uncertain significance	15	83924026	83924026	Human		name
156242314	CV2210649	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2231G>A (p.Arg744Gln)	not specified [RCV004083793]	uncertain significance	15	83942709	83942709	Human		name
156193331	CV2214036	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2872C>T (p.Arg958Trp)	not specified [RCV004084083]	uncertain significance	15	83982500	83982500	Human		name
156049857	CV2241996	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2477G>A (p.Gly826Glu)	not specified [RCV004108943]	uncertain significance	15	83943069	83943069	Human		name
156080849	CV2255970	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2752A>G (p.Ile918Val)	not specified [RCV004122418]	likely benign	15	83982380	83982380	Human		name
156158380	CV2262473	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2840A>G (p.Glu947Gly)	not specified [RCV004128908]	uncertain significance	15	83982468	83982468	Human		name
156073478	CV2263796	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2888A>T (p.Lys963Met)	not specified [RCV004136078]	uncertain significance	15	83982516	83982516	Human		name
155996335	CV2288497	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1592C>T (p.Pro531Leu)	not specified [RCV004152033]	uncertain significance	15	83897982	83897982	Human		name
156296581	CV2297590	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2506G>A (p.Gly836Ser)	not specified [RCV004155292]	uncertain significance	15	83970499	83970499	Human		name
155972872	CV2334377	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1544G>A (p.Gly515Asp)	not specified [RCV004188353]	uncertain significance	15	83897934	83897934	Human		name
156331171	CV2339596	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1762G>A (p.Glu588Lys)	not specified [RCV004196307]	uncertain significance	15	83913153	83913153	Human		name
156292475	CV2340155	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2069G>T (p.Arg690Leu)	not specified [RCV004192392]	uncertain significance	15	83923985	83923985	Human		name
156170615	CV2354885	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2114C>G (p.Pro705Arg)	not specified [RCV004191381]	uncertain significance	15	83924030	83924030	Human		name
155930011	CV2361018	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2785T>G (p.Ser929Ala)	not specified [RCV004216214]	uncertain significance	15	83982413	83982413	Human		name
155930532	CV2366801	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2983C>T (p.Leu995Phe)	not specified [RCV004210791]	uncertain significance	15	83982611	83982611	Human		name
156387244	CV2372686	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1502G>A (p.Arg501Gln)	not specified [RCV004221882]	uncertain significance	15	83897892	83897892	Human		name
155935903	CV2380145	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2671C>G (p.Leu891Val)	not specified [RCV004224519]	uncertain significance	15	83982299	83982299	Human		name
329384219	CV2434994	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2353A>G (p.Thr785Ala)	not specified [RCV004250859]	uncertain significance	15	83942945	83942945	Human		name
329356944	CV2460623	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1061C>T (p.Thr354Met)	not specified [RCV004268889]	uncertain significance	15	83885201	83885201	Human		name
329381113	CV2464512	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2587T>C (p.Cys863Arg)	not specified [RCV004276428]	uncertain significance	15	83970580	83970580	Human		name
401728424	CV2672926	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2591G>A (p.Arg864Lys)	not specified [RCV004283929]	uncertain significance	15	83970584	83970584	Human		name
401730383	CV2680290	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2810G>A (p.Arg937Gln)	not specified [RCV004288544]	uncertain significance	15	83982438	83982438	Human		name
401729486	CV2690272	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1099G>A (p.Val367Met)	not specified [RCV004302274]	uncertain significance	15	83890135	83890135	Human		name
401758568	CV2694167	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1613A>G (p.Lys538Arg)	not specified [RCV004302593]	uncertain significance	15	83898003	83898003	Human		name
401735610	CV2702822	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1453A>G (p.Met485Val)	not specified [RCV004319381]	uncertain significance	15	83892874	83892874	Human		name
401733091	CV2712968	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2932G>A (p.Gly978Ser)	not specified [RCV004314677]	uncertain significance	15	83982560	83982560	Human		name
401770461	CV2715191	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1811T>C (p.Leu604Pro)	not specified [RCV004324545]	uncertain significance	15	83913202	83913202	Human		name
401887989	CV2768936	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2935G>A (p.Val979Met)	not specified [RCV004347034]	uncertain significance	15	83982563	83982563	Human		name
401859763	CV2771827	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2326G>T (p.Gly776Cys)	not specified [RCV004350591]	uncertain significance	15	83942918	83942918	Human		name
405666091	CV3239430	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1832G>T (p.Gly611Val)	not specified [RCV004367674]	uncertain significance	15	83913223	83913223	Human		name
405666101	CV3239432	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1931C>T (p.Thr644Met)	not specified [RCV004367676]	likely benign	15	83913322	83913322	Human		name
405666125	CV3239437	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1939G>A (p.Asp647Asn)	not specified [RCV004367681]	uncertain significance	15	83913330	83913330	Human		name
405666190	CV3239450	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2234A>G (p.Asp745Gly)	not specified [RCV004367694]	uncertain significance	15	83942712	83942712	Human		name
405666223	CV3239457	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2420A>G (p.Lys807Arg)	not specified [RCV004367701]	uncertain significance	15	83943012	83943012	Human		name
405666264	CV3239465	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2586G>T (p.Met862Ile)	not specified [RCV004367709]	uncertain significance	15	83970579	83970579	Human		name
405666405	CV3239492	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2929A>G (p.Ile977Val)	not specified [RCV004367736]	uncertain significance	15	83982557	83982557	Human		name
407471346	CV3425894	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2084G>C (p.Ser695Thr)	not specified [RCV004615670]	uncertain significance	15	83924000	83924000	Human		name
407471512	CV3425935	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2036C>G (p.Thr679Arg)	not specified [RCV004615711]	uncertain significance	15	83923952	83923952	Human		name
407450955	CV3425970	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2360G>A (p.Arg787Gln)	not specified [RCV004607873]	uncertain significance	15	83942952	83942952	Human		name
407450971	CV3425976	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2560C>T (p.Arg854Trp)	not specified [RCV004607879]	uncertain significance	15	83970553	83970553	Human		name
407451029	CV3426003	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1529G>A (p.Gly510Glu)	not specified [RCV004607906]	uncertain significance	15	83897919	83897919	Human		name
597770921	CV3650031	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2046C>G (p.Asp682Glu)	not specified [RCV004897020]	uncertain significance	15	83923962	83923962	Human		name
597770962	CV3650042	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2422G>A (p.Ala808Thr)	not specified [RCV004897029]	uncertain significance	15	83943014	83943014	Human		name
597771048	CV3650063	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2645A>T (p.Lys882Ile)	not specified [RCV004897047]	uncertain significance	15	83982273	83982273	Human		name
597771074	CV3650072	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1973C>A (p.Ala658Glu)	not specified [RCV004897052]	uncertain significance	15	83913364	83913364	Human		name
597770630	CV3653384	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1738T>C (p.Cys580Arg)	not specified [RCV004896956]	uncertain significance	15	83913129	83913129	Human		name
597770634	CV3653390	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1108C>T (p.Arg370Cys)	not specified [RCV004896957]	uncertain significance	15	83890144	83890144	Human		name
597770736	CV3653416	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2704C>G (p.Gln902Glu)	not specified [RCV004896980]	uncertain significance	15	83982332	83982332	Human		name
597770846	CV3653452	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1906A>T (p.Ile636Phe)	not specified [RCV004897004]	uncertain significance	15	83913297	83913297	Human		name
597770865	CV3653493	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1759C>T (p.Arg587Cys)	not specified [RCV004897008]	uncertain significance	15	83913150	83913150	Human		name
598210072	CV3944068	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2056G>T (p.Asp686Tyr)	not specified [RCV005315800]	uncertain significance	15	83923972	83923972	Human		name
598210132	CV3944079	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1286C>T (p.Ala429Val)	not specified [RCV005315810]	uncertain significance	15	83892707	83892707	Human		name
598210193	CV3944090	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2464C>T (p.His822Tyr)	not specified [RCV005315819]	uncertain significance	15	83943056	83943056	Human		name
598210240	CV3944098	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2555A>G (p.Lys852Arg)	not specified [RCV005315826]	uncertain significance	15	83970548	83970548	Human		name
598242091	CV3944118	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1598C>T (p.Pro533Leu)	not specified [RCV005321668]	uncertain significance	15	83897988	83897988	Human		name
598242127	CV3944124	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2387T>C (p.Leu796Ser)	not specified [RCV005321674]	uncertain significance	15	83942979	83942979	Human		name
598209506	CV3947891	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1775G>A (p.Arg592His)	not specified [RCV005315707]	uncertain significance	15	83913166	83913166	Human		name
598209574	CV3947911	single nucleotide variant	NM_207517.3(ADAMTSL3):c.1516A>G (p.Ile506Val)	not specified [RCV005315720]	uncertain significance	15	83897906	83897906	Human		name
598241920	CV3947916	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2107T>G (p.Cys703Gly)	not specified [RCV005321633]	uncertain significance	15	83924023	83924023	Human		name
598209696	CV3947941	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2544G>C (p.Arg848Ser)	not specified [RCV005315742]	uncertain significance	15	83970537	83970537	Human		name
598209978	CV3947994	single nucleotide variant	NM_207517.3(ADAMTSL3):c.2027C>T (p.Thr676Ile)	not specified [RCV005315787]	uncertain significance	15	83923943	83923943	Human		name
8635603	CV90825	single nucleotide variant	NM_207517.2(ADAMTSL3):c.1495C>T (p.Arg499Trp)	Malignant melanoma [RCV000070923]	not provided	15	83897885	83897885	Human		name
150444962	CV1261122	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4979C>T (p.Thr1660Ile)	not provided [RCV001679796]	benign	15	84037709	84037709	Human		name
150465448	CV1277241	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4108A>G (p.Thr1370Ala)	not provided [RCV001710535]	benign	15	84014676	84014676	Human		name
156247844	CV2202979	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4850T>C (p.Phe1617Ser)	not specified [RCV004069239]	uncertain significance	15	84036868	84036868	Human		name
156326855	CV2217154	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4666C>T (p.Arg1556Cys)	not specified [RCV004085823]	uncertain significance	15	84031344	84031344	Human		name
156245859	CV2228257	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4903A>C (p.Lys1635Gln)	not specified [RCV004098270]	uncertain significance	15	84036921	84036921	Human		name
155904387	CV2275908	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3485C>G (p.Ser1162Trp)	not specified [RCV004139565]	uncertain significance	15	83983113	83983113	Human		name
155965917	CV2284135	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4171G>C (p.Glu1391Gln)	not specified [RCV004144728]	uncertain significance	15	84016397	84016397	Human		name
156099504	CV2306548	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4039C>T (p.Leu1347Phe)	not specified [RCV004157157]	uncertain significance	15	84014607	84014607	Human		name
156165889	CV2315198	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3752A>G (p.Gln1251Arg)	not specified [RCV004165370]	likely benign	15	83988726	83988726	Human		name
156290885	CV2324948	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4082A>G (p.Asn1361Ser)	not specified [RCV004175204]	uncertain significance	15	84014650	84014650	Human		name
155980122	CV2336875	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4595G>A (p.Arg1532Gln)	not specified [RCV004190493]	uncertain significance	15	84025375	84025375	Human		name
156172381	CV2337592	single nucleotide variant	NM_207517.3(ADAMTSL3):c.5062T>C (p.Cys1688Arg)	not specified [RCV004181156]	uncertain significance	15	84037792	84037792	Human		name
155925877	CV2348531	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4772A>G (p.Asn1591Ser)	not specified [RCV004193714]	uncertain significance	15	84036790	84036790	Human		name
155989474	CV2371944	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4051T>C (p.Ser1351Pro)	not specified [RCV004221626]	uncertain significance	15	84014619	84014619	Human		name
155989484	CV2371945	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4708G>T (p.Ala1570Ser)	not specified [RCV004221627]	uncertain significance	15	84031386	84031386	Human		name
156144792	CV2393721	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4700G>A (p.Arg1567His)	not specified [RCV004231521]	likely benign	15	84031378	84031378	Human		name
243053596	CV2404677	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4729G>C (p.Asp1577His)	Lung adenocarcinoma [RCV003129704]	uncertain significance	15	84031407	84031407	Human	2	name
329356825	CV2431162	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4337G>A (p.Arg1446His)	not specified [RCV004250513]	uncertain significance	15	84021473	84021473	Human		name
329400960	CV2445923	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3814G>C (p.Asp1272His)	not specified [RCV004270523]	uncertain significance	15	83988788	83988788	Human		name
329394142	CV2450104	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4111A>G (p.Asn1371Asp)	not specified [RCV004269146]	uncertain significance	15	84014679	84014679	Human		name
329395582	CV2458483	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3428A>T (p.Glu1143Val)	not specified [RCV004267891]	uncertain significance	15	83983056	83983056	Human		name
401771133	CV2700878	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3868G>C (p.Glu1290Gln)	not specified [RCV004307148]	uncertain significance	15	83991109	83991109	Human		name
401740706	CV2702595	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4057T>G (p.Leu1353Val)	not specified [RCV004317077]	uncertain significance	15	84014625	84014625	Human		name
401762001	CV2713976	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3245C>T (p.Ala1082Val)	not specified [RCV004315390]	uncertain significance	15	83982873	83982873	Human		name
401783447	CV2723581	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4417G>C (p.Ala1473Pro)	not specified [RCV004323979]	uncertain significance	15	84021553	84021553	Human		name
401767556	CV2729744	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4454C>T (p.Ala1485Val)	not specified [RCV004332765]	uncertain significance	15	84021590	84021590	Human		name
401873842	CV2757749	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3001C>T (p.Arg1001Trp)	not specified [RCV004336898]	uncertain significance	15	83982629	83982629	Human		name
401886397	CV2780342	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3192C>G (p.Ser1064Arg)	not specified [RCV004357747]	uncertain significance	15	83982820	83982820	Human		name
405666490	CV3239508	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3223T>G (p.Leu1075Val)	not specified [RCV004367752]	uncertain significance	15	83982851	83982851	Human		name
405666522	CV3239514	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3292G>A (p.Glu1098Lys)	not specified [RCV004367758]	uncertain significance	15	83982920	83982920	Human		name
405666548	CV3239519	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3566C>T (p.Ser1189Leu)	not specified [RCV004367763]	uncertain significance	15	83983194	83983194	Human		name
405666576	CV3239524	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3778A>G (p.Ile1260Val)	not specified [RCV004367768]	uncertain significance	15	83988752	83988752	Human		name
405666635	CV3239537	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3824G>A (p.Ser1275Asn)	not specified [RCV004367781]	uncertain significance	15	83988798	83988798	Human		name
405666666	CV3239543	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3898C>T (p.His1300Tyr)	not specified [RCV004367787]	uncertain significance	15	83991139	83991139	Human		name
405666677	CV3239545	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3992T>G (p.Ile1331Arg)	not specified [RCV004367789]	uncertain significance	15	84014560	84014560	Human		name
405666730	CV3239555	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4096G>T (p.Val1366Phe)	not specified [RCV004367799]	uncertain significance	15	84014664	84014664	Human		name
405666756	CV3239561	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4129G>A (p.Val1377Met)	not specified [RCV004367805]	likely benign	15	84014697	84014697	Human		name
405666794	CV3239569	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4223C>T (p.Thr1408Ile)	not specified [RCV004367813]	uncertain significance	15	84016449	84016449	Human		name
405666815	CV3239573	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4265C>T (p.Pro1422Leu)	not specified [RCV004367817]	likely benign	15	84016491	84016491	Human		name
405666837	CV3239577	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4276C>T (p.Pro1426Ser)	not specified [RCV004367821]	uncertain significance	15	84021412	84021412	Human		name
405666879	CV3239586	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4561G>T (p.Val1521Leu)	not specified [RCV004367830]	uncertain significance	15	84025341	84025341	Human		name
405666904	CV3239591	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4654C>T (p.Arg1552Trp)	not specified [RCV004367835]	uncertain significance	15	84025434	84025434	Human		name
405666941	CV3239598	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4699C>T (p.Arg1567Cys)	not specified [RCV004367842]	uncertain significance	15	84031377	84031377	Human		name
405666981	CV3239606	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4741G>C (p.Asp1581His)	not specified [RCV004367850]	uncertain significance	15	84031419	84031419	Human		name
405667039	CV3239619	single nucleotide variant	NM_207517.3(ADAMTSL3):c.5027C>T (p.Ser1676Phe)	not specified [RCV004367863]	uncertain significance	15	84037757	84037757	Human		name
407471251	CV3425872	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3610A>G (p.Ile1204Val)	not specified [RCV004615648]	uncertain significance	15	83983238	83983238	Human		name
407471388	CV3425904	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4091C>G (p.Thr1364Ser)	not specified [RCV004615680]	uncertain significance	15	84014659	84014659	Human		name
407471425	CV3425915	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4367A>G (p.Asn1456Ser)	not specified [RCV004615691]	uncertain significance	15	84021503	84021503	Human		name
407471547	CV3425945	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4072T>G (p.Ser1358Ala)	not specified [RCV004615721]	uncertain significance	15	84014640	84014640	Human		name
407451006	CV3425991	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4142T>C (p.Val1381Ala)	not specified [RCV004607894]	uncertain significance	15	84014710	84014710	Human		name
407451027	CV3426001	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4147C>T (p.His1383Tyr)	not specified [RCV004607904]	uncertain significance	15	84014715	84014715	Human		name
597770642	CV3653392	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3099G>T (p.Met1033Ile)	not specified [RCV004896959]	uncertain significance	15	83982727	83982727	Human		name
597770741	CV3653422	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4534C>T (p.Arg1512Trp)	not specified [RCV004896981]	uncertain significance	15	84025314	84025314	Human		name
597770851	CV3653460	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4594C>T (p.Arg1532Trp)	not specified [RCV004897005]	uncertain significance	15	84025374	84025374	Human		name
597770856	CV3653471	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3278C>T (p.Thr1093Ile)	not specified [RCV004897006]	uncertain significance	15	83982906	83982906	Human		name
597770860	CV3653482	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3391G>A (p.Ala1131Thr)	not specified [RCV004897007]	uncertain significance	15	83983019	83983019	Human		name
597770870	CV3653505	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3518A>G (p.Lys1173Arg)	not specified [RCV004897009]	uncertain significance	15	83983146	83983146	Human		name
597770875	CV3653516	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4183G>A (p.Val1395Ile)	not specified [RCV004897010]	uncertain significance	15	84016409	84016409	Human		name
598210028	CV3944061	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3077T>G (p.Leu1026Trp)	not specified [RCV005315794]	uncertain significance	15	83982705	83982705	Human		name
598210109	CV3944075	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4775G>T (p.Cys1592Phe)	not specified [RCV005315806]	uncertain significance	15	84036793	84036793	Human		name
598209557	CV3947905	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4526C>T (p.Thr1509Met)	not specified [RCV005315717]	likely benign	15	84025306	84025306	Human		name
598209619	CV3947923	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3358C>A (p.Leu1120Met)	not specified [RCV005315728]	uncertain significance	15	83982986	83982986	Human		name
598209737	CV3947948	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4441C>T (p.Arg1481Trp)	not specified [RCV005315749]	uncertain significance	15	84021577	84021577	Human		name
598209765	CV3947953	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4999A>G (p.Met1667Val)	not specified [RCV005315754]	uncertain significance	15	84037729	84037729	Human		name
598209805	CV3947962	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3319A>T (p.Met1107Leu)	not specified [RCV005315762]	uncertain significance	15	83982947	83982947	Human		name
15161258	CV703380	single nucleotide variant	NM_207517.3(ADAMTSL3):c.5036G>A (p.Arg1679His)	not provided [RCV000947639]	benign	15	84037766	84037766	Human		name
15198784	CV726306	single nucleotide variant	NM_207517.3(ADAMTSL3):c.3144C>A (p.Asp1048Glu)	not provided [RCV000890456]	benign	15	83982772	83982772	Human		name
15111158	CV726307	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4678C>T (p.Arg1560Cys)	not provided [RCV000894216]	benign	15	84031356	84031356	Human		name
15129708	CV739831	single nucleotide variant	NM_207517.3(ADAMTSL3):c.4673T>C (p.Met1558Thr)	not provided [RCV000897485]	benign	15	84031351	84031351	Human		name
8627715	CV82859	single nucleotide variant	NM_207517.2(ADAMTSL3):c.4196G>A (p.Gly1399Glu)	Malignant melanoma [RCV000062939]	not provided	15	84016422	84016422	Human		name

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