Fgd5 Variant Search Result - Rat Genome Database

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180 records found for search term Fgd5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15182112	CV774781	single nucleotide variant	NM_152536.4(FGD5):c.3264+8C>T	not provided [RCV000930287]	likely benign	3	14901069	14901069	Human		name
15194212	CV759115	single nucleotide variant	NM_152536.4(FGD5):c.2909+10C>G	not provided [RCV000911060]	benign	3	14897679	14897679	Human		name
405759481	CV3253563	single nucleotide variant	NM_152536.4(FGD5):c.8G>C (p.Arg3Thr)	not specified [RCV004393997]	uncertain significance	3	14819079	14819079	Human		name
156336334	CV2333657	single nucleotide variant	NM_152536.4(FGD5):c.10G>T (p.Gly4Cys)	not specified [RCV004192497]	uncertain significance	3	14819081	14819081	Human		name
405759375	CV3253544	single nucleotide variant	NM_152536.4(FGD5):c.14C>T (p.Pro5Leu)	not specified [RCV004393978]	uncertain significance	3	14819085	14819085	Human		name
598241346	CV3955472	single nucleotide variant	NM_152536.4(FGD5):c.13C>T (p.Pro5Ser)	not specified [RCV005344329]	uncertain significance	3	14819084	14819084	Human		name
401731298	CV2701299	single nucleotide variant	NM_152536.4(FGD5):c.49G>A (p.Ala17Thr)	not specified [RCV004311678]	likely benign	3	14819120	14819120	Human		name
401926247	CV2819964	single nucleotide variant	NM_152536.4(FGD5):c.960C>T (p.Ser320=)	not provided [RCV003437709]	likely benign	3	14820031	14820031	Human		name
155905733	CV2283156	single nucleotide variant	NM_152536.4(FGD5):c.227A>T (p.Asp76Val)	not specified [RCV004145839]	uncertain significance	3	14819298	14819298	Human		name
156105843	CV2307500	single nucleotide variant	NM_152536.4(FGD5):c.199G>A (p.Val67Met)	not specified [RCV004166150]	uncertain significance	3	14819270	14819270	Human		name
401717795	CV2704021	single nucleotide variant	NM_152536.4(FGD5):c.240C>A (p.Asp80Glu)	not specified [RCV004308910]	uncertain significance	3	14819311	14819311	Human		name
401884930	CV2766345	single nucleotide variant	NM_152536.4(FGD5):c.215C>T (p.Pro72Leu)	not specified [RCV004342597]	likely benign	3	14819286	14819286	Human		name
401860431	CV2768589	single nucleotide variant	NM_152536.4(FGD5):c.257A>G (p.Asn86Ser)	not specified [RCV004344451]	uncertain significance	3	14819328	14819328	Human		name
401926248	CV2819965	single nucleotide variant	NM_152536.4(FGD5):c.2058C>T (p.Tyr686=)	not provided [RCV003437710]	likely benign	3	14821129	14821129	Human		name
405264299	CV3185296	single nucleotide variant	NM_152536.4(FGD5):c.2721C>T (p.Tyr907=)	not provided [RCV003885860]	likely benign	3	14880745	14880745	Human		name
405759385	CV3253546	single nucleotide variant	NM_152536.4(FGD5):c.157A>G (p.Ile53Val)	not specified [RCV004393980]	likely benign	3	14819228	14819228	Human		name
405759425	CV3253553	single nucleotide variant	NM_152536.4(FGD5):c.277G>A (p.Glu93Lys)	not specified [RCV004393987]	uncertain significance	3	14819348	14819348	Human		name
598241333	CV3955470	single nucleotide variant	NM_152536.4(FGD5):c.2526C>T (p.Ser842=)	not specified [RCV005344327]	likely benign	3	14864128	14864128	Human		name
15149830	CV708628	single nucleotide variant	NM_152536.4(FGD5):c.1224C>T (p.Pro408=)	not provided [RCV000967828]	benign	3	14820295	14820295	Human		name
15150690	CV708629	single nucleotide variant	NM_152536.4(FGD5):c.2460C>T (p.Tyr820=)	not provided [RCV000967993]	benign	3	14821531	14821531	Human		name
15149843	CV708632	single nucleotide variant	NM_152536.4(FGD5):c.2970C>T (p.His990=)	not provided [RCV000967830]	benign	3	14897999	14897999	Human		name
15182107	CV763678	single nucleotide variant	NM_152536.4(FGD5):c.2556C>T (p.Pro852=)	not provided [RCV000930286]	likely benign	3	14864158	14864158	Human		name
8630635	CV85790	single nucleotide variant	NM_152536.4(FGD5):c.2613G>A (p.Ser871=)	not specified [RCV004923727]	likely benign\|not provided	3	14864215	14864215	Human		name
156228147	CV2199383	single nucleotide variant	NM_152536.4(FGD5):c.451G>A (p.Ala151Thr)	not specified [RCV004070955]	uncertain significance	3	14819522	14819522	Human		name
156131400	CV2206352	single nucleotide variant	NM_152536.4(FGD5):c.932C>T (p.Thr311Ile)	not specified [RCV004078685]	uncertain significance	3	14820003	14820003	Human		name
156187541	CV2258284	single nucleotide variant	NM_152536.4(FGD5):c.817G>A (p.Glu273Lys)	not specified [RCV004121650]	uncertain significance	3	14819888	14819888	Human		name
155959294	CV2275759	single nucleotide variant	NM_152536.4(FGD5):c.638C>T (p.Ala213Val)	not specified [RCV004137359]	likely benign	3	14819709	14819709	Human		name
155953103	CV2306334	single nucleotide variant	NM_152536.4(FGD5):c.961G>C (p.Ala321Pro)	not specified [RCV004163043]	uncertain significance	3	14820032	14820032	Human		name
155966125	CV2329767	single nucleotide variant	NM_152536.4(FGD5):c.964G>A (p.Glu322Lys)	not specified [RCV004183240]	uncertain significance	3	14820035	14820035	Human		name
156188807	CV2346870	single nucleotide variant	NM_152536.4(FGD5):c.525G>T (p.Glu175Asp)	not specified [RCV004199865]	uncertain significance	3	14819596	14819596	Human		name
156282132	CV2348832	single nucleotide variant	NM_152536.4(FGD5):c.578A>G (p.Asp193Gly)	not specified [RCV004203276]	uncertain significance	3	14819649	14819649	Human		name
156052879	CV2363537	single nucleotide variant	NM_152536.4(FGD5):c.525G>C (p.Glu175Asp)	not specified [RCV004216106]	uncertain significance	3	14819596	14819596	Human		name
156385208	CV2368214	single nucleotide variant	NM_152536.4(FGD5):c.781G>A (p.Gly261Arg)	not specified [RCV004219014]	uncertain significance	3	14819852	14819852	Human		name
156208093	CV2382448	single nucleotide variant	NM_152536.4(FGD5):c.766A>G (p.Lys256Glu)	not specified [RCV004230783]	uncertain significance	3	14819837	14819837	Human		name
155954917	CV2389844	single nucleotide variant	NM_152536.4(FGD5):c.850G>A (p.Gly284Ser)	not specified [RCV004236064]	uncertain significance	3	14819921	14819921	Human		name
329387875	CV2440193	single nucleotide variant	NM_152536.4(FGD5):c.622G>A (p.Asp208Asn)	not specified [RCV004260644]	uncertain significance	3	14819693	14819693	Human		name
401741019	CV2679857	single nucleotide variant	NM_152536.4(FGD5):c.716C>T (p.Thr239Met)	not specified [RCV004282311]	uncertain significance	3	14819787	14819787	Human		name
401743526	CV2684727	single nucleotide variant	NM_152536.4(FGD5):c.302A>G (p.Glu101Gly)	not specified [RCV004293816]	uncertain significance	3	14819373	14819373	Human		name
401750099	CV2704981	single nucleotide variant	NM_152536.4(FGD5):c.892G>C (p.Asp298His)	not specified [RCV004309588]	uncertain significance	3	14819963	14819963	Human		name
401721630	CV2710076	single nucleotide variant	NM_152536.4(FGD5):c.478G>C (p.Val160Leu)	not specified [RCV004315136]	uncertain significance	3	14819549	14819549	Human		name
401887920	CV2768849	single nucleotide variant	NM_152536.4(FGD5):c.980T>C (p.Ile327Thr)	not specified [RCV004346964]	uncertain significance	3	14820051	14820051	Human		name
401891112	CV2769041	single nucleotide variant	NM_152536.4(FGD5):c.305G>A (p.Arg102His)	not specified [RCV004348910]	likely benign	3	14819376	14819376	Human		name
401895328	CV2786369	single nucleotide variant	NM_152536.4(FGD5):c.428T>G (p.Leu143Arg)	not specified [RCV004361965]	uncertain significance	3	14819499	14819499	Human		name
405759452	CV3253558	single nucleotide variant	NM_152536.4(FGD5):c.377C>T (p.Pro126Leu)	not specified [RCV004393992]	uncertain significance	3	14819448	14819448	Human		name
405759463	CV3253560	single nucleotide variant	NM_152536.4(FGD5):c.619C>T (p.Pro207Ser)	not specified [RCV004393994]	uncertain significance	3	14819690	14819690	Human		name
405759469	CV3253561	single nucleotide variant	NM_152536.4(FGD5):c.648T>G (p.Asp216Glu)	not specified [RCV004393995]	uncertain significance	3	14819719	14819719	Human		name
405759473	CV3253562	single nucleotide variant	NM_152536.4(FGD5):c.668G>C (p.Ser223Thr)	not specified [RCV004393996]	uncertain significance	3	14819739	14819739	Human		name
597751393	CV3672604	single nucleotide variant	NM_152536.4(FGD5):c.739G>A (p.Glu247Lys)	not specified [RCV004923719]	uncertain significance	3	14819810	14819810	Human		name
597751403	CV3672607	single nucleotide variant	NM_152536.4(FGD5):c.823C>G (p.Leu275Val)	not specified [RCV004923721]	uncertain significance	3	14819894	14819894	Human		name
597751415	CV3672609	single nucleotide variant	NM_152536.4(FGD5):c.967G>A (p.Glu323Lys)	not specified [RCV004923723]	uncertain significance	3	14820038	14820038	Human		name
597751420	CV3672610	single nucleotide variant	NM_152536.4(FGD5):c.953A>T (p.Asp318Val)	not specified [RCV004923724]	uncertain significance	3	14820024	14820024	Human		name
597751430	CV3672612	single nucleotide variant	NM_152536.4(FGD5):c.631G>A (p.Gly211Arg)	not specified [RCV004923726]	uncertain significance	3	14819702	14819702	Human		name
598241238	CV3955455	single nucleotide variant	NM_152536.4(FGD5):c.461C>T (p.Pro154Leu)	not specified [RCV005344312]	uncertain significance	3	14819532	14819532	Human		name
598241301	CV3955465	single nucleotide variant	NM_152536.4(FGD5):c.3522C>T (p.Tyr1174=)	not specified [RCV005344322]	likely benign	3	14918786	14918786	Human		name
598241314	CV3955467	single nucleotide variant	NM_152536.4(FGD5):c.828G>C (p.Glu276Asp)	not specified [RCV005344324]	uncertain significance	3	14819899	14819899	Human		name
15133181	CV708643	single nucleotide variant	NM_152536.4(FGD5):c.3786T>C (p.His1262=)	not provided [RCV000964905]	benign	3	14922527	14922527	Human		name
156227120	CV2203186	single nucleotide variant	NM_152536.4(FGD5):c.1597G>T (p.Ala533Ser)	not specified [RCV004070883]	uncertain significance	3	14820668	14820668	Human		name
156256701	CV2204527	single nucleotide variant	NM_152536.4(FGD5):c.1289A>G (p.Tyr430Cys)	not specified [RCV004081646]	uncertain significance	3	14820360	14820360	Human		name
156276239	CV2209756	single nucleotide variant	NM_152536.4(FGD5):c.1204G>A (p.Gly402Ser)	not specified [RCV004083072]	uncertain significance	3	14820275	14820275	Human		name
156379465	CV2217886	single nucleotide variant	NM_152536.4(FGD5):c.1471G>A (p.Gly491Ser)	not specified [RCV004086350]	uncertain significance	3	14820542	14820542	Human		name
155969139	CV2244453	single nucleotide variant	NM_152536.4(FGD5):c.1897T>C (p.Ser633Pro)	not specified [RCV004100418]	uncertain significance	3	14820968	14820968	Human		name
156114274	CV2268534	single nucleotide variant	NM_152536.4(FGD5):c.2192A>T (p.Lys731Ile)	not specified [RCV004130218]	uncertain significance	3	14821263	14821263	Human		name
156336441	CV2270736	single nucleotide variant	NM_152536.4(FGD5):c.2257T>C (p.Phe753Leu)	not specified [RCV004131797]	uncertain significance	3	14821328	14821328	Human		name
156139939	CV2280787	single nucleotide variant	NM_152536.4(FGD5):c.2340G>T (p.Met780Ile)	not specified [RCV004145049]	uncertain significance	3	14821411	14821411	Human		name
156099853	CV2294667	single nucleotide variant	NM_152536.4(FGD5):c.2356A>G (p.Asn786Asp)	not specified [RCV004161917]	uncertain significance	3	14821427	14821427	Human		name
156302617	CV2319646	single nucleotide variant	NM_152536.4(FGD5):c.1003A>G (p.Met335Val)	not specified [RCV004185191]	likely benign	3	14820074	14820074	Human		name
156285972	CV2334893	single nucleotide variant	NM_152536.4(FGD5):c.1684G>A (p.Val562Met)	not specified [RCV004182000]	uncertain significance	3	14820755	14820755	Human		name
156222606	CV2343972	single nucleotide variant	NM_152536.4(FGD5):c.1225G>A (p.Ala409Thr)	not specified [RCV004195591]	uncertain significance	3	14820296	14820296	Human		name
155922784	CV2347381	single nucleotide variant	NM_152536.4(FGD5):c.1772C>T (p.Ser591Phe)	not specified [RCV004207221]	uncertain significance	3	14820843	14820843	Human		name
156279438	CV2348337	single nucleotide variant	NM_152536.4(FGD5):c.1823C>T (p.Thr608Met)	not specified [RCV004193534]	uncertain significance	3	14820894	14820894	Human		name
156089072	CV2359330	single nucleotide variant	NM_152536.4(FGD5):c.1697C>T (p.Pro566Leu)	not specified [RCV004212612]	uncertain significance	3	14820768	14820768	Human		name
156282378	CV2363120	single nucleotide variant	NM_152536.4(FGD5):c.2341A>G (p.Asn781Asp)	not specified [RCV004211244]	uncertain significance	3	14821412	14821412	Human		name
155938201	CV2364987	single nucleotide variant	NM_152536.4(FGD5):c.1917G>C (p.Glu639Asp)	not specified [RCV004222280]	uncertain significance	3	14820988	14820988	Human		name
155953501	CV2379022	single nucleotide variant	NM_152536.4(FGD5):c.2105A>G (p.Asn702Ser)	not specified [RCV004233783]	uncertain significance	3	14821176	14821176	Human		name
329354699	CV2444728	single nucleotide variant	NM_152536.4(FGD5):c.1760G>A (p.Cys587Tyr)	not specified [RCV004258982]	uncertain significance	3	14820831	14820831	Human		name
401728302	CV2672866	single nucleotide variant	NM_152536.4(FGD5):c.2392G>A (p.Gly798Ser)	not specified [RCV004282037]	uncertain significance	3	14821463	14821463	Human		name
401729741	CV2683782	single nucleotide variant	NM_152536.4(FGD5):c.1834A>G (p.Met612Val)	not specified [RCV004284517]	likely benign	3	14820905	14820905	Human		name
401728582	CV2693651	single nucleotide variant	NM_152536.4(FGD5):c.1696C>G (p.Pro566Ala)	not specified [RCV004297988]	uncertain significance	3	14820767	14820767	Human		name
401778257	CV2718614	single nucleotide variant	NM_152536.4(FGD5):c.1390T>C (p.Cys464Arg)	not specified [RCV004320197]	uncertain significance	3	14820461	14820461	Human		name
401862974	CV2775421	single nucleotide variant	NM_152536.4(FGD5):c.1611G>T (p.Leu537Phe)	not specified [RCV004348819]	uncertain significance	3	14820682	14820682	Human		name
405759352	CV3253540	single nucleotide variant	NM_152536.4(FGD5):c.1235A>T (p.Asp412Val)	not specified [RCV004393974]	uncertain significance	3	14820306	14820306	Human		name
405759357	CV3253541	single nucleotide variant	NM_152536.4(FGD5):c.1295T>C (p.Met432Thr)	not specified [RCV004393975]	uncertain significance	3	14820366	14820366	Human		name
405759363	CV3253542	single nucleotide variant	NM_152536.4(FGD5):c.1334G>C (p.Gly445Ala)	not specified [RCV004393976]	uncertain significance	3	14820405	14820405	Human		name
405759368	CV3253543	single nucleotide variant	NM_152536.4(FGD5):c.1354G>A (p.Ala452Thr)	not specified [RCV004393977]	likely benign	3	14820425	14820425	Human		name
405759379	CV3253545	single nucleotide variant	NM_152536.4(FGD5):c.1565C>T (p.Thr522Met)	not specified [RCV004393979]	uncertain significance	3	14820636	14820636	Human		name
405759392	CV3253547	single nucleotide variant	NM_152536.4(FGD5):c.1613C>T (p.Pro538Leu)	not specified [RCV004393981]	uncertain significance	3	14820684	14820684	Human		name
405759398	CV3253548	single nucleotide variant	NM_152536.4(FGD5):c.1828T>C (p.Ser610Pro)	not specified [RCV004393982]	uncertain significance	3	14820899	14820899	Human		name
405759404	CV3253549	single nucleotide variant	NM_152536.4(FGD5):c.1928C>T (p.Pro643Leu)	not specified [RCV004393983]	uncertain significance	3	14820999	14820999	Human		name
405759409	CV3253550	single nucleotide variant	NM_152536.4(FGD5):c.2183G>C (p.Gly728Ala)	not specified [RCV004393984]	uncertain significance	3	14821254	14821254	Human		name
405759414	CV3253551	single nucleotide variant	NM_152536.4(FGD5):c.2306C>T (p.Ala769Val)	not specified [RCV004393985]	uncertain significance	3	14821377	14821377	Human		name
405759419	CV3253552	single nucleotide variant	NM_152536.4(FGD5):c.2734C>G (p.Gln912Glu)	not specified [RCV004393986]	uncertain significance	3	14880758	14880758	Human		name
407501310	CV3439088	single nucleotide variant	NM_152536.4(FGD5):c.1870A>G (p.Ile624Val)	not specified [RCV004623230]	uncertain significance	3	14820941	14820941	Human		name
407501315	CV3439089	single nucleotide variant	NM_152536.4(FGD5):c.1439C>T (p.Thr480Met)	not specified [RCV004623231]	uncertain significance	3	14820510	14820510	Human		name
407501319	CV3439090	single nucleotide variant	NM_152536.4(FGD5):c.1979C>T (p.Thr660Met)	not specified [RCV004623232]	uncertain significance	3	14821050	14821050	Human		name
407501352	CV3439096	single nucleotide variant	NM_152536.4(FGD5):c.2499G>C (p.Gln833His)	not specified [RCV004623238]	uncertain significance	3	14821570	14821570	Human		name
407501357	CV3439097	single nucleotide variant	NM_152536.4(FGD5):c.2089C>T (p.Arg697Trp)	not specified [RCV004623239]	uncertain significance	3	14821160	14821160	Human		name
407501361	CV3439098	single nucleotide variant	NM_152536.4(FGD5):c.2419C>G (p.Gln807Glu)	not specified [RCV004623240]	uncertain significance	3	14821490	14821490	Human		name
407501365	CV3439099	single nucleotide variant	NM_152536.4(FGD5):c.1777G>A (p.Gly593Arg)	not specified [RCV004623241]	uncertain significance	3	14820848	14820848	Human		name
407501370	CV3439100	single nucleotide variant	NM_152536.4(FGD5):c.1604G>C (p.Arg535Thr)	not specified [RCV004623242]	uncertain significance	3	14820675	14820675	Human		name
407501385	CV3439103	single nucleotide variant	NM_152536.4(FGD5):c.1238T>G (p.Val413Gly)	not specified [RCV004623245]	uncertain significance	3	14820309	14820309	Human		name
407501391	CV3439104	single nucleotide variant	NM_152536.4(FGD5):c.1583G>A (p.Gly528Glu)	not specified [RCV004623246]	uncertain significance	3	14820654	14820654	Human		name
597751388	CV3672603	single nucleotide variant	NM_152536.4(FGD5):c.1916A>G (p.Glu639Gly)	not specified [RCV004923718]	uncertain significance	3	14820987	14820987	Human		name
597751441	CV3672614	single nucleotide variant	NM_152536.4(FGD5):c.2187G>T (p.Lys729Asn)	not specified [RCV004923729]	uncertain significance	3	14821258	14821258	Human		name
597751447	CV3672615	single nucleotide variant	NM_152536.4(FGD5):c.1489G>T (p.Val497Phe)	not specified [RCV004923730]	uncertain significance	3	14820560	14820560	Human		name
597751462	CV3672618	single nucleotide variant	NM_152536.4(FGD5):c.2857C>T (p.His953Tyr)	not specified [RCV004923733]	uncertain significance	3	14897617	14897617	Human		name
597751467	CV3672619	single nucleotide variant	NM_152536.4(FGD5):c.1972G>C (p.Ala658Pro)	not specified [RCV004923734]	uncertain significance	3	14821043	14821043	Human		name
598241232	CV3955454	single nucleotide variant	NM_152536.4(FGD5):c.1757C>T (p.Ser586Leu)	not specified [RCV005344311]	uncertain significance	3	14820828	14820828	Human		name
598241246	CV3955456	single nucleotide variant	NM_152536.4(FGD5):c.1438A>G (p.Thr480Ala)	not specified [RCV005344313]	uncertain significance	3	14820509	14820509	Human		name
598241252	CV3955457	single nucleotide variant	NM_152536.4(FGD5):c.2554C>A (p.Pro852Thr)	not specified [RCV005344314]	uncertain significance	3	14864156	14864156	Human		name
598241272	CV3955460	single nucleotide variant	NM_152536.4(FGD5):c.1804C>T (p.Pro602Ser)	not specified [RCV005344317]	uncertain significance	3	14820875	14820875	Human		name
598241279	CV3955461	single nucleotide variant	NM_152536.4(FGD5):c.2886G>C (p.Glu962Asp)	not specified [RCV005344318]	uncertain significance	3	14897646	14897646	Human		name
598241295	CV3955464	single nucleotide variant	NM_152536.4(FGD5):c.1534A>T (p.Ile512Phe)	not specified [RCV005344321]	uncertain significance	3	14820605	14820605	Human		name
598241308	CV3955466	single nucleotide variant	NM_152536.4(FGD5):c.2248C>T (p.Arg750Trp)	not specified [RCV005344323]	uncertain significance	3	14821319	14821319	Human		name
598241321	CV3955468	single nucleotide variant	NM_152536.4(FGD5):c.2446G>A (p.Glu816Lys)	not specified [RCV005344325]	uncertain significance	3	14821517	14821517	Human		name
598241207	CV3959392	single nucleotide variant	NM_152536.4(FGD5):c.2971G>A (p.Ala991Thr)	not specified [RCV005344307]	uncertain significance	3	14898000	14898000	Human		name
598241226	CV3959395	single nucleotide variant	NM_152536.4(FGD5):c.2689G>A (p.Ala897Thr)	not specified [RCV005344310]	uncertain significance	3	14880602	14880602	Human		name
15103816	CV697875	single nucleotide variant	NM_152536.4(FGD5):c.1798C>T (p.His600Tyr)	not provided [RCV000959557]	benign	3	14820869	14820869	Human		name
15186643	CV697876	single nucleotide variant	NM_152536.4(FGD5):c.2482G>A (p.Ala828Thr)	not provided [RCV000953346]	benign	3	14821553	14821553	Human		name
15144556	CV708627	single nucleotide variant	NM_152536.4(FGD5):c.1207G>A (p.Gly403Arg)	not provided [RCV000966852]	benign	3	14820278	14820278	Human		name
15149837	CV708630	single nucleotide variant	NM_152536.4(FGD5):c.2518G>A (p.Ala840Thr)	not provided [RCV000967829]	benign	3	14821589	14821589	Human		name
156177942	CV2201551	single nucleotide variant	NM_152536.4(FGD5):c.3691A>G (p.Ser1231Gly)	not specified [RCV004080042]	uncertain significance	3	14922432	14922432	Human		name
156129563	CV2209826	single nucleotide variant	NM_152536.4(FGD5):c.3985G>A (p.Gly1329Ser)	not specified [RCV004076290]	likely benign	3	14924055	14924055	Human		name
156064580	CV2228991	single nucleotide variant	NM_152536.4(FGD5):c.4118G>A (p.Cys1373Tyr)	not specified [RCV004098778]	uncertain significance	3	14926119	14926119	Human		name
156142797	CV2257410	single nucleotide variant	NM_152536.4(FGD5):c.4051C>A (p.Pro1351Thr)	not specified [RCV004125495]	uncertain significance	3	14924121	14924121	Human		name
156002051	CV2257918	single nucleotide variant	NM_152536.4(FGD5):c.4055C>T (p.Ser1352Leu)	not specified [RCV004129738]	uncertain significance	3	14924125	14924125	Human		name
156358907	CV2260867	single nucleotide variant	NM_152536.4(FGD5):c.3392G>A (p.Arg1131Gln)	not specified [RCV004125767]	uncertain significance	3	14910916	14910916	Human		name
156238731	CV2268967	single nucleotide variant	NM_152536.4(FGD5):c.3941G>A (p.Arg1314Gln)	not specified [RCV004128369]	uncertain significance	3	14924011	14924011	Human		name
156049991	CV2271845	single nucleotide variant	NM_152536.4(FGD5):c.3619C>T (p.Pro1207Ser)	not specified [RCV004130670]	uncertain significance	3	14921967	14921967	Human		name
156267138	CV2275527	single nucleotide variant	NM_152536.4(FGD5):c.4309C>G (p.Leu1437Val)	not specified [RCV004137173]	uncertain significance	3	14932688	14932688	Human		name
155920948	CV2276220	single nucleotide variant	NM_152536.4(FGD5):c.3082G>A (p.Gly1028Ser)	not specified [RCV004142168]	uncertain significance	3	14898754	14898754	Human		name
155918413	CV2283540	single nucleotide variant	NM_152536.4(FGD5):c.3316G>A (p.Asp1106Asn)	not specified [RCV004139749]	uncertain significance	3	14907691	14907691	Human		name
156133059	CV2284555	single nucleotide variant	NM_152536.4(FGD5):c.3897G>T (p.Glu1299Asp)	not specified [RCV004140727]	uncertain significance	3	14923135	14923135	Human		name
155992367	CV2286191	single nucleotide variant	NM_152536.4(FGD5):c.3412G>A (p.Asp1138Asn)	not specified [RCV004146157]	uncertain significance	3	14917255	14917255	Human		name
155965226	CV2286900	single nucleotide variant	NM_152536.4(FGD5):c.4025C>G (p.Ser1342Trp)	not specified [RCV004144514]	uncertain significance	3	14924095	14924095	Human		name
156015979	CV2299035	single nucleotide variant	NM_152536.4(FGD5):c.3575G>A (p.Cys1192Tyr)	not specified [RCV004158555]	uncertain significance	3	14921923	14921923	Human		name
156151344	CV2307549	single nucleotide variant	NM_152536.4(FGD5):c.3103C>T (p.Arg1035Trp)	not specified [RCV004166189]	uncertain significance	3	14898775	14898775	Human		name
155973973	CV2334496	single nucleotide variant	NM_152536.4(FGD5):c.4082G>C (p.Gly1361Ala)	not specified [RCV004188462]	uncertain significance	3	14926083	14926083	Human		name
156086954	CV2336858	single nucleotide variant	NM_152536.4(FGD5):c.3233C>T (p.Thr1078Ile)	not specified [RCV004190477]	uncertain significance	3	14901030	14901030	Human		name
156288350	CV2370639	single nucleotide variant	NM_152536.4(FGD5):c.3425A>G (p.Tyr1142Cys)	not specified [RCV004215960]	uncertain significance	3	14917268	14917268	Human		name
156111717	CV2387837	single nucleotide variant	NM_152536.4(FGD5):c.3962C>T (p.Pro1321Leu)	not specified [RCV004234351]	uncertain significance	3	14924032	14924032	Human		name
156166482	CV2398933	single nucleotide variant	NM_152536.4(FGD5):c.3603T>G (p.Cys1201Trp)	not specified [RCV004245247]	uncertain significance	3	14921951	14921951	Human		name
156002415	CV2399544	single nucleotide variant	NM_152536.4(FGD5):c.3113G>A (p.Arg1038Gln)	not specified [RCV004242798]	uncertain significance	3	14898785	14898785	Human		name
329392057	CV2470335	single nucleotide variant	NM_152536.4(FGD5):c.4004T>C (p.Val1335Ala)	not specified [RCV004279725]	uncertain significance	3	14924074	14924074	Human		name
401740202	CV2684294	single nucleotide variant	NM_152536.4(FGD5):c.3796G>A (p.Ala1266Thr)	not specified [RCV004288949]	uncertain significance	3	14922537	14922537	Human		name
401746995	CV2698756	single nucleotide variant	NM_152536.4(FGD5):c.3091A>G (p.Thr1031Ala)	not specified [RCV004301208]	uncertain significance	3	14898763	14898763	Human		name
401736587	CV2703189	single nucleotide variant	NM_152536.4(FGD5):c.4287T>G (p.Phe1429Leu)	not specified [RCV004315254]	uncertain significance	3	14932666	14932666	Human		name
401770371	CV2711115	single nucleotide variant	NM_152536.4(FGD5):c.3030C>G (p.His1010Gln)	not specified [RCV004310797]	uncertain significance	3	14898059	14898059	Human		name
401773406	CV2716556	single nucleotide variant	NM_152536.4(FGD5):c.4043A>G (p.Lys1348Arg)	not specified [RCV004327632]	uncertain significance	3	14924113	14924113	Human		name
401728610	CV2729690	single nucleotide variant	NM_152536.4(FGD5):c.3301G>A (p.Val1101Ile)	not specified [RCV004331948]	uncertain significance	3	14907676	14907676	Human		name
401876425	CV2760769	single nucleotide variant	NM_152536.4(FGD5):c.4114C>T (p.Arg1372Trp)	not specified [RCV004336413]	uncertain significance	3	14926115	14926115	Human		name
401891211	CV2778556	single nucleotide variant	NM_152536.4(FGD5):c.3025C>T (p.Leu1009Phe)	not specified [RCV004344210]	uncertain significance	3	14898054	14898054	Human		name
401896765	CV2788759	single nucleotide variant	NM_152536.4(FGD5):c.3433C>T (p.Pro1145Ser)	not specified [RCV004361227]	uncertain significance	3	14917276	14917276	Human		name
401922158	CV2819966	single nucleotide variant	NM_152536.4(FGD5):c.3544G>A (p.Glu1182Lys)	not provided [RCV003433486]	likely benign	3	14918808	14918808	Human		name
405759437	CV3253555	single nucleotide variant	NM_152536.4(FGD5):c.3239G>T (p.Arg1080Leu)	not specified [RCV004393989]	uncertain significance	3	14901036	14901036	Human		name
405759442	CV3253556	single nucleotide variant	NM_152536.4(FGD5):c.3433C>G (p.Pro1145Ala)	not specified [RCV004393990]	uncertain significance	3	14917276	14917276	Human		name
405759447	CV3253557	single nucleotide variant	NM_152536.4(FGD5):c.3454C>T (p.Arg1152Trp)	not specified [RCV004393991]	uncertain significance	3	14917297	14917297	Human		name
405759458	CV3253559	single nucleotide variant	NM_152536.4(FGD5):c.4376C>T (p.Ala1459Val)	not specified [RCV004393993]	uncertain significance	3	14933154	14933154	Human		name
407501305	CV3439087	single nucleotide variant	NM_152536.4(FGD5):c.3112C>T (p.Arg1038Trp)	not specified [RCV004623229]	uncertain significance	3	14898784	14898784	Human		name
407501329	CV3439092	single nucleotide variant	NM_152536.4(FGD5):c.3781C>T (p.Arg1261Cys)	not specified [RCV004623234]	uncertain significance	3	14922522	14922522	Human		name
407501335	CV3439093	single nucleotide variant	NM_152536.4(FGD5):c.4360G>A (p.Glu1454Lys)	not specified [RCV004623235]	uncertain significance	3	14933138	14933138	Human		name
407501340	CV3439094	single nucleotide variant	NM_152536.4(FGD5):c.3829C>T (p.Arg1277Trp)	not specified [RCV004623236]	uncertain significance	3	14923067	14923067	Human		name
407501347	CV3439095	single nucleotide variant	NM_152536.4(FGD5):c.3542C>G (p.Ser1181Cys)	not specified [RCV004623237]	uncertain significance	3	14918806	14918806	Human		name
407501376	CV3439101	single nucleotide variant	NM_152536.4(FGD5):c.4288C>T (p.His1430Tyr)	not specified [RCV004623243]	uncertain significance	3	14932667	14932667	Human		name
597751369	CV3672599	single nucleotide variant	NM_152536.4(FGD5):c.3037C>T (p.Arg1013Trp)	not specified [RCV004923714]	uncertain significance	3	14898066	14898066	Human		name
597751373	CV3672600	single nucleotide variant	NM_152536.4(FGD5):c.3301G>T (p.Val1101Phe)	not specified [RCV004923715]	uncertain significance	3	14907676	14907676	Human		name
597751378	CV3672601	single nucleotide variant	NM_152536.4(FGD5):c.3289A>G (p.Ile1097Val)	not specified [RCV004923716]	uncertain significance	3	14907664	14907664	Human		name
597751383	CV3672602	single nucleotide variant	NM_152536.4(FGD5):c.3940C>T (p.Arg1314Trp)	not specified [RCV004923717]	uncertain significance	3	14924010	14924010	Human		name
597751409	CV3672608	single nucleotide variant	NM_152536.4(FGD5):c.4246C>T (p.Pro1416Ser)	not specified [RCV004923722]	uncertain significance	3	14932625	14932625	Human		name
597751425	CV3672611	single nucleotide variant	NM_152536.4(FGD5):c.4025C>T (p.Ser1342Leu)	not specified [RCV004923725]	uncertain significance	3	14924095	14924095	Human		name
597751435	CV3672613	single nucleotide variant	NM_152536.4(FGD5):c.3386G>A (p.Arg1129Gln)	not specified [RCV004923728]	uncertain significance	3	14910910	14910910	Human		name
597751457	CV3672617	single nucleotide variant	NM_152536.4(FGD5):c.3101A>G (p.His1034Arg)	not specified [RCV004923732]	uncertain significance	3	14898773	14898773	Human		name
597751472	CV3672620	single nucleotide variant	NM_152536.4(FGD5):c.3795C>G (p.His1265Gln)	not specified [RCV004923735]	uncertain significance	3	14922536	14922536	Human		name
597751477	CV3672621	single nucleotide variant	NM_152536.4(FGD5):c.3686G>A (p.Gly1229Glu)	not specified [RCV004923736]	uncertain significance	3	14922427	14922427	Human		name
598241260	CV3955458	single nucleotide variant	NM_152536.4(FGD5):c.4282A>G (p.Ile1428Val)	not specified [RCV005344315]	likely benign	3	14932661	14932661	Human		name
598241266	CV3955459	single nucleotide variant	NM_152536.4(FGD5):c.3406A>G (p.Met1136Val)	not specified [RCV005344316]	uncertain significance	3	14917249	14917249	Human		name
598241285	CV3955462	single nucleotide variant	NM_152536.4(FGD5):c.3640G>C (p.Ala1214Pro)	not specified [RCV005344319]	uncertain significance	3	14921988	14921988	Human		name
598241326	CV3955469	single nucleotide variant	NM_152536.4(FGD5):c.4052C>T (p.Pro1351Leu)	not specified [RCV005344326]	uncertain significance	3	14924122	14924122	Human		name
598241341	CV3955471	single nucleotide variant	NM_152536.4(FGD5):c.3356C>T (p.Thr1119Met)	not specified [RCV005344328]	uncertain significance	3	14910880	14910880	Human		name
598241214	CV3959393	single nucleotide variant	NM_152536.4(FGD5):c.3305G>A (p.Arg1102Gln)	not specified [RCV005344308]	uncertain significance	3	14907680	14907680	Human		name
598241219	CV3959394	single nucleotide variant	NM_152536.4(FGD5):c.4115G>A (p.Arg1372Gln)	not specified [RCV005344309]	uncertain significance	3	14926116	14926116	Human		name

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