Ncan Variant Search Result - Rat Genome Database

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159 records found for search term Ncan

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597647831	CV3562238	single nucleotide variant	NM_004386.3(NCAN):c.11C>A (p.Pro4Gln)	not specified [RCV004826448]	uncertain significance	19	19216964	19216964	Human		name
156060523	CV2280182	single nucleotide variant	NM_004386.3(NCAN):c.91G>A (p.Asp31Asn)	not specified [RCV004140406]	uncertain significance	19	19218932	19218932	Human		name
401878917	CV2754879	single nucleotide variant	NM_004386.3(NCAN):c.89C>A (p.Thr30Asn)	not specified [RCV004341353]	uncertain significance	19	19218930	19218930	Human		name
401884129	CV2765050	single nucleotide variant	NM_004386.3(NCAN):c.76A>G (p.Thr26Ala)	not specified [RCV004337169]	uncertain significance	19	19218917	19218917	Human		name
407521183	CV3458287	single nucleotide variant	NM_004386.3(NCAN):c.85A>G (p.Ile29Val)	not specified [RCV004652445]	uncertain significance	19	19218926	19218926	Human		name
597647790	CV3562231	single nucleotide variant	NM_004386.3(NCAN):c.80A>G (p.Gln27Arg)	not specified [RCV004826442]	uncertain significance	19	19218921	19218921	Human		name
598252789	CV3983635	single nucleotide variant	NM_004386.3(NCAN):c.55T>C (p.Phe19Leu)	not specified [RCV005385226]	likely benign	19	19217008	19217008	Human		name
598216520	CV3983638	single nucleotide variant	NM_004386.3(NCAN):c.36G>C (p.Leu12Phe)	not specified [RCV005378927]	uncertain significance	19	19216989	19216989	Human		name
15120316	CV716316	single nucleotide variant	NM_004386.3(NCAN):c.372G>A (p.Thr124=)	not provided [RCV000962702]	benign	19	19219213	19219213	Human		name
156259970	CV2204779	single nucleotide variant	NM_004386.3(NCAN):c.251C>T (p.Ala84Val)	not specified [RCV004075039]	uncertain significance	19	19219092	19219092	Human		name
156047114	CV2336342	single nucleotide variant	NM_004386.3(NCAN):c.263G>A (p.Arg88Gln)	not specified [RCV004194565]	uncertain significance	19	19219104	19219104	Human		name
329376300	CV2438081	single nucleotide variant	NM_004386.3(NCAN):c.117G>A (p.Met39Ile)	not specified [RCV004256869]	uncertain significance	19	19218958	19218958	Human		name
401861675	CV2756406	single nucleotide variant	NM_004386.3(NCAN):c.245G>A (p.Arg82Gln)	not specified [RCV004342947]	uncertain significance	19	19219086	19219086	Human		name
401892580	CV2782242	single nucleotide variant	NM_004386.3(NCAN):c.245G>T (p.Arg82Leu)	not specified [RCV004359210]	uncertain significance	19	19219086	19219086	Human		name
597647761	CV3562226	single nucleotide variant	NM_004386.3(NCAN):c.197G>A (p.Arg66Gln)	not specified [RCV004826438]	uncertain significance	19	19219038	19219038	Human		name
598252772	CV3983630	single nucleotide variant	NM_004386.3(NCAN):c.254C>T (p.Ser85Leu)	not specified [RCV005385223]	uncertain significance	19	19219095	19219095	Human		name
617153108	CV4021081	single nucleotide variant	NM_004386.3(NCAN):c.1155C>G (p.Pro385=)	not provided [RCV005428834]	likely benign	19	19226568	19226568	Human		name
8636698	CV91923	single nucleotide variant	NM_004386.2(NCAN):c.1296C>T (p.Thr432=)	Malignant melanoma [RCV000072021]	not provided	19	19226709	19226709	Human		name
156114786	CV2225187	single nucleotide variant	NM_004386.3(NCAN):c.553A>G (p.Ser185Gly)	not specified [RCV004094988]	uncertain significance	19	19224098	19224098	Human		name
156257644	CV2264896	single nucleotide variant	NM_004386.3(NCAN):c.635C>T (p.Ser212Phe)	not specified [RCV004134645]	uncertain significance	19	19224180	19224180	Human		name
156168366	CV2320080	single nucleotide variant	NM_004386.3(NCAN):c.661A>G (p.Thr221Ala)	not specified [RCV004167931]	uncertain significance	19	19224316	19224316	Human		name
156361292	CV2326468	single nucleotide variant	NM_004386.3(NCAN):c.502C>T (p.Arg168Trp)	not specified [RCV004183030]	uncertain significance	19	19224047	19224047	Human		name
156392078	CV2378269	single nucleotide variant	NM_004386.3(NCAN):c.776G>T (p.Gly259Val)	not specified [RCV004226304]	uncertain significance	19	19224431	19224431	Human		name
155906739	CV2379121	single nucleotide variant	NM_004386.3(NCAN):c.359G>A (p.Arg120Gln)	not specified [RCV004235918]	uncertain significance	19	19219200	19219200	Human		name
156162127	CV2398321	single nucleotide variant	NM_004386.3(NCAN):c.460C>G (p.Pro154Ala)	not specified [RCV004235224]	uncertain significance	19	19219301	19219301	Human		name
401774782	CV2688285	single nucleotide variant	NM_004386.3(NCAN):c.322C>A (p.Gln108Lys)	not specified [RCV004299295]	uncertain significance	19	19219163	19219163	Human		name
401896785	CV2788780	single nucleotide variant	NM_004386.3(NCAN):c.460C>T (p.Pro154Ser)	not specified [RCV004361243]	uncertain significance	19	19219301	19219301	Human		name
405795203	CV3336405	single nucleotide variant	NM_004386.3(NCAN):c.640C>T (p.Arg214Cys)	not specified [RCV004475458]	uncertain significance	19	19224185	19224185	Human		name
405795245	CV3336418	single nucleotide variant	NM_004386.3(NCAN):c.842G>T (p.Arg281Leu)	not specified [RCV004475471]	uncertain significance	19	19225040	19225040	Human		name
405795270	CV3336426	single nucleotide variant	NM_004386.3(NCAN):c.968G>T (p.Arg323Leu)	not specified [RCV004475479]	uncertain significance	19	19225166	19225166	Human		name
407488409	CV3458277	single nucleotide variant	NM_004386.3(NCAN):c.692G>A (p.Arg231His)	not specified [RCV004641269]	uncertain significance	19	19224347	19224347	Human		name
407488425	CV3458279	single nucleotide variant	NM_004386.3(NCAN):c.311C>T (p.Ala104Val)	not specified [RCV004641271]	uncertain significance	19	19219152	19219152	Human		name
597647817	CV3562235	single nucleotide variant	NM_004386.3(NCAN):c.683A>T (p.Tyr228Phe)	not specified [RCV004826446]	uncertain significance	19	19224338	19224338	Human		name
597647852	CV3562241	single nucleotide variant	NM_004386.3(NCAN):c.568G>A (p.Ala190Thr)	not specified [RCV004826451]	uncertain significance	19	19224113	19224113	Human		name
597647881	CV3562245	single nucleotide variant	NM_004386.3(NCAN):c.314A>G (p.Lys105Arg)	not specified [RCV004826455]	uncertain significance	19	19219155	19219155	Human		name
598216315	CV3983621	single nucleotide variant	NM_004386.3(NCAN):c.688G>A (p.Asp230Asn)	not specified [RCV005378920]	uncertain significance	19	19224343	19224343	Human		name
598252745	CV3983624	single nucleotide variant	NM_004386.3(NCAN):c.771G>T (p.Glu257Asp)	not specified [RCV005385218]	uncertain significance	19	19224426	19224426	Human		name
598252757	CV3983627	single nucleotide variant	NM_004386.3(NCAN):c.696C>G (p.Ser232Arg)	not specified [RCV005385220]	uncertain significance	19	19224351	19224351	Human		name
598252783	CV3983634	single nucleotide variant	NM_004386.3(NCAN):c.712C>T (p.Arg238Trp)	not specified [RCV005385225]	uncertain significance	19	19224367	19224367	Human		name
598252795	CV3983637	single nucleotide variant	NM_004386.3(NCAN):c.805C>A (p.Arg269Ser)	not specified [RCV005385227]	uncertain significance	19	19225003	19225003	Human		name
598216538	CV3983643	single nucleotide variant	NM_004386.3(NCAN):c.877C>G (p.Leu293Val)	not specified [RCV005378929]	uncertain significance	19	19225075	19225075	Human		name
598216545	CV3983645	single nucleotide variant	NM_004386.3(NCAN):c.728G>T (p.Arg243Leu)	not specified [RCV005378930]	uncertain significance	19	19224383	19224383	Human		name
15194819	CV704869	single nucleotide variant	NM_004386.3(NCAN):c.3828T>G (p.Arg1276=)	not provided [RCV000955749]	benign	19	19249773	19249773	Human		name
15148690	CV741738	single nucleotide variant	NM_004386.3(NCAN):c.3114C>T (p.Phe1038=)	not provided [RCV000900774]	benign	19	19233883	19233883	Human		name
8636701	CV91926	single nucleotide variant	NM_004386.2(NCAN):c.3537G>A (p.Ala1179=)	Malignant melanoma [RCV000072024]	not provided	19	19245357	19245357	Human		name
155990364	CV2255497	single nucleotide variant	NM_004386.3(NCAN):c.2374G>C (p.Ala792Pro)	not specified [RCV004119933]	likely benign	19	19227994	19227994	Human		name
155947088	CV2262547	single nucleotide variant	NM_004386.3(NCAN):c.1726A>G (p.Ile576Val)	not specified [RCV004130757]	uncertain significance	19	19227346	19227346	Human		name
155906089	CV2283341	single nucleotide variant	NM_004386.3(NCAN):c.2135G>A (p.Ser712Asn)	not specified [RCV004145998]	uncertain significance	19	19227755	19227755	Human		name
156260752	CV2287445	single nucleotide variant	NM_004386.3(NCAN):c.1346G>T (p.Ser449Ile)	not specified [RCV004140917]	uncertain significance	19	19226759	19226759	Human		name
156056333	CV2308892	single nucleotide variant	NM_004386.3(NCAN):c.2901G>T (p.Glu967Asp)	not specified [RCV004169184]	uncertain significance	19	19228521	19228521	Human		name
156179972	CV2331426	single nucleotide variant	NM_004386.3(NCAN):c.1346G>A (p.Ser449Asn)	not specified [RCV004184060]	uncertain significance	19	19226759	19226759	Human		name
156324815	CV2335103	single nucleotide variant	NM_004386.3(NCAN):c.1783G>A (p.Ala595Thr)	not specified [RCV004184639]	uncertain significance	19	19227403	19227403	Human		name
156184227	CV2335540	single nucleotide variant	NM_004386.3(NCAN):c.2563G>A (p.Glu855Lys)	not specified [RCV004193753]	uncertain significance	19	19228183	19228183	Human		name
156168345	CV2345406	single nucleotide variant	NM_004386.3(NCAN):c.2750C>T (p.Pro917Leu)	not specified [RCV004198182]	uncertain significance	19	19228370	19228370	Human		name
156143781	CV2358603	single nucleotide variant	NM_004386.3(NCAN):c.2504C>T (p.Pro835Leu)	not specified [RCV004207480]	likely benign	19	19228124	19228124	Human		name
155926785	CV2365813	single nucleotide variant	NM_004386.3(NCAN):c.1129G>T (p.Gly377Trp)	not specified [RCV004214348]	uncertain significance	19	19226542	19226542	Human		name
156223625	CV2394988	single nucleotide variant	NM_004386.3(NCAN):c.1385C>A (p.Thr462Asn)	not specified [RCV004236683]	uncertain significance	19	19226798	19226798	Human		name
329377911	CV2436075	single nucleotide variant	NM_004386.3(NCAN):c.2621C>T (p.Thr874Met)	not specified [RCV004255292]	uncertain significance	19	19228241	19228241	Human		name
329362236	CV2444501	single nucleotide variant	NM_004386.3(NCAN):c.2125G>A (p.Gly709Arg)	not specified [RCV004256730]	uncertain significance	19	19227745	19227745	Human		name
401722580	CV2677040	single nucleotide variant	NM_004386.3(NCAN):c.1988C>A (p.Ala663Asp)	not specified [RCV004293639]	uncertain significance	19	19227608	19227608	Human		name
401718280	CV2700293	single nucleotide variant	NM_004386.3(NCAN):c.2614C>G (p.Pro872Ala)	not specified [RCV004310956]	uncertain significance	19	19228234	19228234	Human		name
401734709	CV2709586	single nucleotide variant	NM_004386.3(NCAN):c.2131A>G (p.Thr711Ala)	not specified [RCV004318814]	uncertain significance	19	19227751	19227751	Human		name
401782505	CV2719849	single nucleotide variant	NM_004386.3(NCAN):c.2101C>T (p.Pro701Ser)	not specified [RCV004329264]	uncertain significance	19	19227721	19227721	Human		name
401878886	CV2754866	single nucleotide variant	NM_004386.3(NCAN):c.2255G>T (p.Gly752Val)	not specified [RCV004341341]	uncertain significance	19	19227875	19227875	Human		name
401867108	CV2759100	single nucleotide variant	NM_004386.3(NCAN):c.1169T>C (p.Leu390Pro)	not specified [RCV004342401]	uncertain significance	19	19226582	19226582	Human		name
401862443	CV2762086	single nucleotide variant	NM_004386.3(NCAN):c.2840G>A (p.Gly947Glu)	not specified [RCV004341903]	uncertain significance	19	19228460	19228460	Human		name
401886301	CV2771160	single nucleotide variant	NM_004386.3(NCAN):c.2855C>T (p.Pro952Leu)	not specified [RCV004346155]	uncertain significance	19	19228475	19228475	Human		name
401895898	CV2775804	single nucleotide variant	NM_004386.3(NCAN):c.2698G>A (p.Glu900Lys)	not specified [RCV004344846]	uncertain significance	19	19228318	19228318	Human		name
405788022	CV3340017	single nucleotide variant	NM_004386.3(NCAN):c.1009C>T (p.Arg337Cys)	not specified [RCV004473253]	uncertain significance	19	19225207	19225207	Human		name
405788033	CV3340020	single nucleotide variant	NM_004386.3(NCAN):c.1087T>C (p.Ser363Pro)	not specified [RCV004473256]	likely benign	19	19226500	19226500	Human		name
405788092	CV3340032	single nucleotide variant	NM_004386.3(NCAN):c.1202C>T (p.Thr401Ile)	not specified [RCV004473268]	uncertain significance	19	19226615	19226615	Human		name
405788145	CV3340043	single nucleotide variant	NM_004386.3(NCAN):c.1510A>T (p.Met504Leu)	not specified [RCV004473279]	likely benign	19	19226923	19226923	Human		name
405788168	CV3340048	single nucleotide variant	NM_004386.3(NCAN):c.1534A>G (p.Thr512Ala)	not specified [RCV004473284]	uncertain significance	19	19226947	19226947	Human		name
405788192	CV3340053	single nucleotide variant	NM_004386.3(NCAN):c.1613G>A (p.Arg538Gln)	not specified [RCV004473289]	likely benign	19	19227026	19227026	Human		name
405788219	CV3340059	single nucleotide variant	NM_004386.3(NCAN):c.1650G>A (p.Met550Ile)	not specified [RCV004473295]	uncertain significance	19	19227063	19227063	Human		name
405788261	CV3340068	single nucleotide variant	NM_004386.3(NCAN):c.1813T>C (p.Ser605Pro)	not specified [RCV004473304]	uncertain significance	19	19227433	19227433	Human		name
405788364	CV3340087	single nucleotide variant	NM_004386.3(NCAN):c.2203G>A (p.Ala735Thr)	not specified [RCV004473323]	uncertain significance	19	19227823	19227823	Human		name
405788383	CV3340091	single nucleotide variant	NM_004386.3(NCAN):c.2350T>C (p.Ser784Pro)	not specified [RCV004473327]	uncertain significance	19	19227970	19227970	Human		name
405788415	CV3340098	single nucleotide variant	NM_004386.3(NCAN):c.2426A>G (p.Lys809Arg)	not specified [RCV004473334]	uncertain significance	19	19228046	19228046	Human		name
405788494	CV3340116	single nucleotide variant	NM_004386.3(NCAN):c.2612C>T (p.Thr871Met)	not specified [RCV004473352]	uncertain significance	19	19228232	19228232	Human		name
405788544	CV3340127	single nucleotide variant	NM_004386.3(NCAN):c.2732C>T (p.Ser911Leu)	not specified [RCV004473363]	likely benign	19	19228352	19228352	Human		name
407488417	CV3458278	single nucleotide variant	NM_004386.3(NCAN):c.2420T>C (p.Val807Ala)	not specified [RCV004641270]	uncertain significance	19	19228040	19228040	Human		name
407521174	CV3458280	single nucleotide variant	NM_004386.3(NCAN):c.1295C>A (p.Thr432Asn)	not specified [RCV004652442]	uncertain significance	19	19226708	19226708	Human		name
407521177	CV3458282	single nucleotide variant	NM_004386.3(NCAN):c.1120G>C (p.Gly374Arg)	not specified [RCV004652443]	uncertain significance	19	19226533	19226533	Human		name
407488438	CV3458283	single nucleotide variant	NM_004386.3(NCAN):c.2989G>A (p.Gly997Arg)	not specified [RCV004641273]	uncertain significance	19	19228609	19228609	Human		name
407488445	CV3458284	single nucleotide variant	NM_004386.3(NCAN):c.1493C>T (p.Pro498Leu)	not specified [RCV004641274]	uncertain significance	19	19226906	19226906	Human		name
597647714	CV3562219	single nucleotide variant	NM_004386.3(NCAN):c.2222C>T (p.Thr741Ile)	not specified [RCV004826431]	uncertain significance	19	19227842	19227842	Human		name
597647721	CV3562220	single nucleotide variant	NM_004386.3(NCAN):c.1378G>A (p.Ala460Thr)	not specified [RCV004826432]	uncertain significance	19	19226791	19226791	Human		name
597647729	CV3562221	single nucleotide variant	NM_004386.3(NCAN):c.1829C>T (p.Thr610Ile)	not specified [RCV004826433]	uncertain significance	19	19227449	19227449	Human		name
597647744	CV3562223	single nucleotide variant	NM_004386.3(NCAN):c.1102C>G (p.Leu368Val)	not specified [RCV004826435]	uncertain significance	19	19226515	19226515	Human		name
597647750	CV3562224	single nucleotide variant	NM_004386.3(NCAN):c.1897A>T (p.Met633Leu)	not specified [RCV004826436]	uncertain significance	19	19227517	19227517	Human		name
597647755	CV3562225	single nucleotide variant	NM_004386.3(NCAN):c.1174C>A (p.Pro392Thr)	not specified [RCV004826437]	uncertain significance	19	19226587	19226587	Human		name
597647769	CV3562227	single nucleotide variant	NM_004386.3(NCAN):c.1382G>A (p.Gly461Asp)	not specified [RCV004826439]	uncertain significance	19	19226795	19226795	Human		name
597647776	CV3562228	single nucleotide variant	NM_004386.3(NCAN):c.1220C>A (p.Pro407His)	not specified [RCV004826440]	uncertain significance	19	19226633	19226633	Human		name
597647782	CV3562230	single nucleotide variant	NM_004386.3(NCAN):c.2681G>A (p.Ser894Asn)	not specified [RCV004826441]	uncertain significance	19	19228301	19228301	Human		name
597647796	CV3562232	single nucleotide variant	NM_004386.3(NCAN):c.1424C>A (p.Pro475His)	not specified [RCV004826443]	uncertain significance	19	19226837	19226837	Human		name
597647803	CV3562233	single nucleotide variant	NM_004386.3(NCAN):c.1403C>G (p.Thr468Arg)	not specified [RCV004826444]	uncertain significance	19	19226816	19226816	Human		name
597647810	CV3562234	single nucleotide variant	NM_004386.3(NCAN):c.2437A>G (p.Asn813Asp)	not specified [RCV004826445]	uncertain significance	19	19228057	19228057	Human		name
597647824	CV3562236	single nucleotide variant	NM_004386.3(NCAN):c.2174G>A (p.Ser725Asn)	not specified [RCV004826447]	uncertain significance	19	19227794	19227794	Human		name
597647858	CV3562242	single nucleotide variant	NM_004386.3(NCAN):c.2446C>T (p.Pro816Ser)	not specified [RCV004826452]	uncertain significance	19	19228066	19228066	Human		name
597647866	CV3562243	single nucleotide variant	NM_004386.3(NCAN):c.1994C>T (p.Ala665Val)	not specified [RCV004826453]	uncertain significance	19	19227614	19227614	Human		name
597647874	CV3562244	single nucleotide variant	NM_004386.3(NCAN):c.1169T>G (p.Leu390Arg)	not specified [RCV004826454]	uncertain significance	19	19226582	19226582	Human		name
597647888	CV3562246	single nucleotide variant	NM_004386.3(NCAN):c.2725G>A (p.Gly909Arg)	not specified [RCV004826456]	uncertain significance	19	19228345	19228345	Human		name
598216307	CV3983620	single nucleotide variant	NM_004386.3(NCAN):c.1550T>G (p.Val517Gly)	not specified [RCV005378919]	likely benign	19	19226963	19226963	Human		name
598216324	CV3983622	single nucleotide variant	NM_004386.3(NCAN):c.1270G>A (p.Glu424Lys)	not specified [RCV005378921]	uncertain significance	19	19226683	19226683	Human		name
598216332	CV3983623	single nucleotide variant	NM_004386.3(NCAN):c.2789C>T (p.Pro930Leu)	not specified [RCV005378922]	uncertain significance	19	19228409	19228409	Human		name
598252751	CV3983626	single nucleotide variant	NM_004386.3(NCAN):c.2631G>T (p.Glu877Asp)	not specified [RCV005385219]	likely benign	19	19228251	19228251	Human		name
598252762	CV3983628	single nucleotide variant	NM_004386.3(NCAN):c.2341C>T (p.Pro781Ser)	not specified [RCV005385221]	uncertain significance	19	19227961	19227961	Human		name
598252806	CV3983640	single nucleotide variant	NM_004386.3(NCAN):c.2182C>T (p.Pro728Ser)	not specified [RCV005385229]	uncertain significance	19	19227802	19227802	Human		name
598216529	CV3983641	single nucleotide variant	NM_004386.3(NCAN):c.1957G>A (p.Glu653Lys)	not specified [RCV005378928]	uncertain significance	19	19227577	19227577	Human		name
598252811	CV3983642	single nucleotide variant	NM_004386.3(NCAN):c.1729T>G (p.Ser577Ala)	not specified [RCV005385230]	uncertain significance	19	19227349	19227349	Human		name
156062296	CV2203509	single nucleotide variant	NM_004386.3(NCAN):c.3134T>C (p.Ile1045Thr)	not specified [RCV004072716]	uncertain significance	19	19233903	19233903	Human		name
156232897	CV2227712	single nucleotide variant	NM_004386.3(NCAN):c.3576C>A (p.Ser1192Arg)	not specified [RCV004094099]	uncertain significance	19	19245396	19245396	Human		name
156078235	CV2230342	single nucleotide variant	NM_004386.3(NCAN):c.3427A>T (p.Thr1143Ser)	not specified [RCV004099943]	uncertain significance	19	19240620	19240620	Human		name
156295785	CV2233764	single nucleotide variant	NM_004386.3(NCAN):c.3815C>T (p.Thr1272Ile)	not specified [RCV004100203]	uncertain significance	19	19248877	19248877	Human		name
156161061	CV2272560	single nucleotide variant	NM_004386.3(NCAN):c.3755A>T (p.His1252Leu)	not specified [RCV004133451]	uncertain significance	19	19248817	19248817	Human		name
156251906	CV2273448	single nucleotide variant	NM_004386.3(NCAN):c.3682G>A (p.Gly1228Ser)	not specified [RCV004132203]	uncertain significance	19	19248744	19248744	Human		name
156259405	CV2274113	single nucleotide variant	NM_004386.3(NCAN):c.3350G>A (p.Arg1117His)	not specified [RCV004134758]	uncertain significance	19	19238352	19238352	Human		name
156265294	CV2275387	single nucleotide variant	NM_004386.3(NCAN):c.3569A>T (p.His1190Leu)	not specified [RCV004135269]	uncertain significance	19	19245389	19245389	Human		name
156010198	CV2290986	single nucleotide variant	NM_004386.3(NCAN):c.3499G>C (p.Glu1167Gln)	not specified [RCV004151537]	uncertain significance	19	19245319	19245319	Human		name
156060721	CV2305431	single nucleotide variant	NM_004386.3(NCAN):c.3818A>G (p.Lys1273Arg)	not specified [RCV004165155]	uncertain significance	19	19248880	19248880	Human		name
156295811	CV2310343	single nucleotide variant	NM_004386.3(NCAN):c.3337G>A (p.Glu1113Lys)	not specified [RCV004163391]	uncertain significance	19	19238339	19238339	Human		name
156288914	CV2327455	single nucleotide variant	NM_004386.3(NCAN):c.3464A>C (p.Asp1155Ala)	not specified [RCV004174869]	uncertain significance	19	19240657	19240657	Human		name
156224874	CV2352615	single nucleotide variant	NM_004386.3(NCAN):c.3827G>A (p.Arg1276His)	not specified [RCV004198648]	uncertain significance	19	19249772	19249772	Human		name
156108285	CV2355390	single nucleotide variant	NM_004386.3(NCAN):c.3302G>A (p.Arg1101His)	not specified [RCV004205249]	uncertain significance	19	19238304	19238304	Human		name
156382877	CV2362984	single nucleotide variant	NM_004386.3(NCAN):c.3038A>G (p.Glu1013Gly)	not specified [RCV004211128]	uncertain significance	19	19233807	19233807	Human		name
329385570	CV2462052	single nucleotide variant	NM_004386.3(NCAN):c.3118G>A (p.Gly1040Arg)	not specified [RCV004266093]	uncertain significance	19	19233887	19233887	Human		name
329397943	CV2466468	single nucleotide variant	NM_004386.3(NCAN):c.3355C>T (p.Arg1119Cys)	not specified [RCV004274020]	uncertain significance	19	19238357	19238357	Human		name
401750635	CV2701429	single nucleotide variant	NM_004386.3(NCAN):c.3658G>A (p.Ala1220Thr)	not specified [RCV004311785]	uncertain significance	19	19248720	19248720	Human		name
401748762	CV2704403	single nucleotide variant	NM_004386.3(NCAN):c.3613C>T (p.Pro1205Ser)	not specified [RCV004311370]	uncertain significance	19	19245433	19245433	Human		name
401774551	CV2713541	single nucleotide variant	NM_004386.3(NCAN):c.3577G>A (p.Gly1193Arg)	not specified [RCV004319136]	uncertain significance	19	19245397	19245397	Human		name
401767182	CV2718232	single nucleotide variant	NM_004386.3(NCAN):c.3841C>T (p.Arg1281Trp)	not specified [RCV004316224]	uncertain significance	19	19249786	19249786	Human		name
401888757	CV2754984	single nucleotide variant	NM_004386.3(NCAN):c.3077A>G (p.Asn1026Ser)	not specified [RCV004341449]	uncertain significance	19	19233846	19233846	Human		name
13211174	CV275535	single nucleotide variant	NM_004386.3(NCAN):c.3115G>A (p.Ala1039Thr)	Developmental dyslexia [RCV000497994]	likely pathogenic\|uncertain significance	19	19233884	19233884	Human	1	name
401876855	CV2793258	single nucleotide variant	NM_004386.3(NCAN):c.3826C>T (p.Arg1276Cys)	not specified [RCV004362086]	uncertain significance	19	19249771	19249771	Human		name
405866957	CV2842474	single nucleotide variant	NM_004386.3(NCAN):c.3864A>T (p.Gln1288His)	EBV-positive nodal T- and NK-cell lymphoma [RCV004557831]	likely benign	19	19249809	19249809	Human		name
405795080	CV3336367	single nucleotide variant	NM_004386.3(NCAN):c.3701A>T (p.Tyr1234Phe)	not specified [RCV004475420]	uncertain significance	19	19248763	19248763	Human		name
405795086	CV3336369	single nucleotide variant	NM_004386.3(NCAN):c.3715A>C (p.Thr1239Pro)	not specified [RCV004475422]	uncertain significance	19	19248777	19248777	Human		name
405795143	CV3336386	single nucleotide variant	NM_004386.3(NCAN):c.3949G>A (p.Glu1317Lys)	not specified [RCV004475439]	uncertain significance	19	19249894	19249894	Human		name
405788613	CV3340141	single nucleotide variant	NM_004386.3(NCAN):c.3011C>T (p.Ala1004Val)	not specified [RCV004473377]	uncertain significance	19	19228631	19228631	Human		name
405788686	CV3340157	single nucleotide variant	NM_004386.3(NCAN):c.3151C>T (p.Leu1051Phe)	not specified [RCV004473393]	uncertain significance	19	19234997	19234997	Human		name
405794972	CV3340165	single nucleotide variant	NM_004386.3(NCAN):c.3233G>A (p.Gly1078Asp)	not specified [RCV004475384]	uncertain significance	19	19235079	19235079	Human		name
405794985	CV3340170	single nucleotide variant	NM_004386.3(NCAN):c.3268C>T (p.Arg1090Cys)	not specified [RCV004475389]	uncertain significance	19	19238270	19238270	Human		name
405795046	CV3340191	single nucleotide variant	NM_004386.3(NCAN):c.3487G>A (p.Gly1163Arg)	not specified [RCV004475410]	uncertain significance	19	19240680	19240680	Human		name
407521170	CV3458276	single nucleotide variant	NM_004386.3(NCAN):c.3226T>A (p.Tyr1076Asn)	not specified [RCV004652441]	uncertain significance	19	19235072	19235072	Human		name
407488432	CV3458281	single nucleotide variant	NM_004386.3(NCAN):c.3511G>A (p.Glu1171Lys)	not specified [RCV004641272]	uncertain significance	19	19245331	19245331	Human		name
407488451	CV3458286	single nucleotide variant	NM_004386.3(NCAN):c.3278A>G (p.His1093Arg)	not specified [RCV004641275]	uncertain significance	19	19238280	19238280	Human		name
597647706	CV3562217	single nucleotide variant	NM_004386.3(NCAN):c.3835C>T (p.Arg1279Trp)	not specified [RCV004826430]	uncertain significance	19	19249780	19249780	Human		name
597647736	CV3562222	single nucleotide variant	NM_004386.3(NCAN):c.3428C>T (p.Thr1143Met)	not specified [RCV004826434]	uncertain significance	19	19240621	19240621	Human		name
597647838	CV3562239	single nucleotide variant	NM_004386.3(NCAN):c.3022C>T (p.His1008Tyr)	not specified [RCV004826449]	uncertain significance	19	19233791	19233791	Human		name
597647845	CV3562240	single nucleotide variant	NM_004386.3(NCAN):c.3301C>T (p.Arg1101Cys)	not specified [RCV004826450]	uncertain significance	19	19238303	19238303	Human		name
598252768	CV3983629	single nucleotide variant	NM_004386.3(NCAN):c.3353G>A (p.Arg1118His)	not specified [RCV005385222]	uncertain significance	19	19238355	19238355	Human		name
598216497	CV3983631	single nucleotide variant	NM_004386.3(NCAN):c.3359C>T (p.Ser1120Phe)	not specified [RCV005378924]	uncertain significance	19	19238361	19238361	Human		name
598216504	CV3983632	single nucleotide variant	NM_004386.3(NCAN):c.3867C>A (p.His1289Gln)	not specified [RCV005378925]	uncertain significance	19	19249812	19249812	Human		name
598252777	CV3983633	single nucleotide variant	NM_004386.3(NCAN):c.3806T>C (p.Ile1269Thr)	not specified [RCV005385224]	uncertain significance	19	19248868	19248868	Human		name
598252801	CV3983639	single nucleotide variant	NM_004386.3(NCAN):c.3005C>T (p.Ala1002Val)	not specified [RCV005385228]	uncertain significance	19	19228625	19228625	Human		name
598252817	CV3983644	single nucleotide variant	NM_004386.3(NCAN):c.3836G>A (p.Arg1279Gln)	not specified [RCV005385231]	uncertain significance	19	19249781	19249781	Human		name
8636699	CV91924	single nucleotide variant	NM_004386.2(NCAN):c.3326G>A (p.Trp1109Ter)	Malignant melanoma [RCV000072022]	not provided	19	19238328	19238328	Human		name
8636700	CV91925	single nucleotide variant	NM_004386.2(NCAN):c.3327G>A (p.Trp1109Ter)	Malignant melanoma [RCV000072023]	not provided	19	19238329	19238329	Human		name

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