Ngfr Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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56 records found for search term Ngfr

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15196430	CV760594	single nucleotide variant	NM_002507.4(NGFR):c.67-4C>T	not provided [RCV000911694]	benign	17	49502059	49502059	Human		name
15116037	CV760450	single nucleotide variant	NM_002507.4(NGFR):c.568+9G>A	not provided [RCV000917555]	likely benign	17	49506667	49506667	Human		name
15157914	CV731154	single nucleotide variant	NM_002507.4(NGFR):c.822-10C>G	not provided [RCV000880907]	benign	17	49511882	49511882	Human		name
329400535	CV2438456	single nucleotide variant	NM_002507.4(NGFR):c.79G>T (p.Gly27Cys)	not specified [RCV004259606]	uncertain significance	17	49502075	49502075	Human		name
597657303	CV3559223	single nucleotide variant	NM_002507.4(NGFR):c.71C>A (p.Ser24Tyr)	not specified [RCV004834389]	uncertain significance	17	49502067	49502067	Human		name
598192567	CV3997763	single nucleotide variant	NM_002507.4(NGFR):c.83C>A (p.Ala28Asp)	not specified [RCV005374373]	uncertain significance	17	49502079	49502079	Human		name
598238435	CV3997765	single nucleotide variant	NM_002507.4(NGFR):c.34G>C (p.Gly12Arg)	not specified [RCV005382746]	uncertain significance	17	49495451	49495451	Human		name
15099223	CV704201	single nucleotide variant	NM_002507.4(NGFR):c.879G>A (p.Thr293=)	not provided [RCV000958726]	benign	17	49511949	49511949	Human		name
15197897	CV727249	single nucleotide variant	NM_002507.4(NGFR):c.333C>T (p.Tyr111=)	not provided [RCV000890197]	benign	17	49506423	49506423	Human		name
15149249	CV755926	single nucleotide variant	NM_002507.4(NGFR):c.318G>A (p.Val106=)	not provided [RCV000923250]	likely benign	17	49506408	49506408	Human		name
15106583	CV755927	single nucleotide variant	NM_002507.4(NGFR):c.630C>T (p.Pro210=)	not provided [RCV000915782]	likely benign	17	49510473	49510473	Human		name
156149602	CV2307419	single nucleotide variant	NM_002507.4(NGFR):c.179A>G (p.Asn60Ser)	not specified [RCV004166091]	uncertain significance	17	49502175	49502175	Human		name
407526946	CV3451306	single nucleotide variant	NM_002507.4(NGFR):c.121G>A (p.Gly41Ser)	not specified [RCV004654998]	uncertain significance	17	49502117	49502117	Human		name
597657288	CV3559225	single nucleotide variant	NM_002507.4(NGFR):c.227T>C (p.Val76Ala)	not specified [RCV004834391]	uncertain significance	17	49506317	49506317	Human		name
15176574	CV715526	single nucleotide variant	NM_002507.4(NGFR):c.1185C>T (p.Ser395=)	not provided [RCV000973217]	benign\|likely benign	17	49512910	49512910	Human		name
15197616	CV727250	single nucleotide variant	NM_002507.4(NGFR):c.1089G>A (p.Ala363=)	not provided [RCV000890110]	likely benign	17	49512814	49512814	Human		name
15197742	CV755928	single nucleotide variant	NM_002507.4(NGFR):c.1092C>T (p.Gly364=)	not provided [RCV000912059]	benign	17	49512817	49512817	Human		name
156161186	CV2236430	single nucleotide variant	NM_002507.4(NGFR):c.410C>G (p.Ser137Cys)	not specified [RCV004108104]	uncertain significance	17	49506500	49506500	Human		name
156046875	CV2244743	single nucleotide variant	NM_002507.4(NGFR):c.892G>C (p.Gly298Arg)	not specified [RCV004102735]	uncertain significance	17	49511962	49511962	Human		name
156257676	CV2277678	single nucleotide variant	NM_002507.4(NGFR):c.514G>C (p.Asp172His)	not specified [RCV004147130]	uncertain significance	17	49506604	49506604	Human		name
156087113	CV2299091	single nucleotide variant	NM_002507.4(NGFR):c.635C>A (p.Thr212Asn)	not specified [RCV004152452]	uncertain significance	17	49510478	49510478	Human		name
156208549	CV2304291	single nucleotide variant	NM_002507.4(NGFR):c.544C>T (p.Arg182Cys)	not specified [RCV004164414]	uncertain significance	17	49506634	49506634	Human		name
156267340	CV2305021	single nucleotide variant	NM_002507.4(NGFR):c.734G>A (p.Arg245Gln)	not specified [RCV004168910]	uncertain significance	17	49510577	49510577	Human		name
156149884	CV2307440	single nucleotide variant	NM_002507.4(NGFR):c.989A>G (p.Lys330Arg)	not specified [RCV004166107]	uncertain significance	17	49512714	49512714	Human		name
155968707	CV2312869	single nucleotide variant	NM_002507.4(NGFR):c.328G>T (p.Ala110Ser)	not specified [RCV004171361]	uncertain significance	17	49506418	49506418	Human		name
156249691	CV2314179	single nucleotide variant	NM_002507.4(NGFR):c.565G>C (p.Glu189Gln)	not specified [RCV004166260]	uncertain significance	17	49506655	49506655	Human		name
156157609	CV2363715	single nucleotide variant	NM_002507.4(NGFR):c.601C>G (p.Pro201Ala)	not specified [RCV004216659]	uncertain significance	17	49510444	49510444	Human		name
156161566	CV2371489	single nucleotide variant	NM_002507.4(NGFR):c.385G>A (p.Glu129Lys)	not specified [RCV004216742]	uncertain significance	17	49506475	49506475	Human		name
156083600	CV2394989	single nucleotide variant	NM_002507.4(NGFR):c.348T>A (p.Asp116Glu)	not specified [RCV004236684]	uncertain significance	17	49506438	49506438	Human		name
329375729	CV2441094	single nucleotide variant	NM_002507.4(NGFR):c.553G>A (p.Asp185Asn)	not specified [RCV004263501]	uncertain significance	17	49506643	49506643	Human		name
329391103	CV2452036	single nucleotide variant	NM_002507.4(NGFR):c.628C>T (p.Pro210Ser)	not specified [RCV004278766]	uncertain significance	17	49510471	49510471	Human		name
401769380	CV2689684	single nucleotide variant	NM_002507.4(NGFR):c.592C>T (p.Arg198Trp)	not specified [RCV004297604]	uncertain significance	17	49510435	49510435	Human		name
401722376	CV2706492	single nucleotide variant	NM_002507.4(NGFR):c.752T>C (p.Leu251Pro)	not specified [RCV004317307]	uncertain significance	17	49510595	49510595	Human		name
401875720	CV2766978	single nucleotide variant	NM_002507.4(NGFR):c.892G>A (p.Gly298Arg)	not specified [RCV004343362]	uncertain significance	17	49511962	49511962	Human		name
405675476	CV3354911	single nucleotide variant	NM_002507.4(NGFR):c.533G>T (p.Arg178Leu)	not specified [RCV004487538]	uncertain significance	17	49506623	49506623	Human		name
405675619	CV3354937	single nucleotide variant	NM_002507.4(NGFR):c.862C>T (p.Arg288Trp)	not specified [RCV004487564]	uncertain significance	17	49511932	49511932	Human		name
407496996	CV3451307	single nucleotide variant	NM_002507.4(NGFR):c.991G>A (p.Gly331Ser)	not specified [RCV004643640]	uncertain significance	17	49512716	49512716	Human		name
407526949	CV3451308	single nucleotide variant	NM_002507.4(NGFR):c.740C>T (p.Thr247Ile)	not specified [RCV004654999]	uncertain significance	17	49510583	49510583	Human		name
597657343	CV3559217	single nucleotide variant	NM_002507.4(NGFR):c.496C>T (p.Pro166Ser)	not specified [RCV004834383]	uncertain significance	17	49506586	49506586	Human		name
597657336	CV3559218	single nucleotide variant	NM_002507.4(NGFR):c.745G>A (p.Asp249Asn)	not specified [RCV004834384]	uncertain significance	17	49510588	49510588	Human		name
597657321	CV3559220	single nucleotide variant	NM_002507.4(NGFR):c.478C>T (p.His160Tyr)	not specified [RCV004834386]	uncertain significance	17	49506568	49506568	Human		name
597657316	CV3559221	single nucleotide variant	NM_002507.4(NGFR):c.322C>T (p.Arg108Cys)	not specified [RCV004834387]	uncertain significance	17	49506412	49506412	Human		name
597657308	CV3559222	single nucleotide variant	NM_002507.4(NGFR):c.751C>T (p.Leu251Phe)	not specified [RCV004834388]	uncertain significance	17	49510594	49510594	Human		name
597657298	CV3559224	single nucleotide variant	NM_002507.4(NGFR):c.925G>A (p.Val309Met)	not specified [RCV004834390]	uncertain significance	17	49511995	49511995	Human		name
597657277	CV3559227	single nucleotide variant	NM_002507.4(NGFR):c.890A>G (p.Glu297Gly)	not specified [RCV004834393]	uncertain significance	17	49511960	49511960	Human		name
597657269	CV3559228	single nucleotide variant	NM_002507.4(NGFR):c.737G>C (p.Gly246Ala)	not specified [RCV004834394]	uncertain significance	17	49510580	49510580	Human		name
15134630	CV740846	single nucleotide variant	NM_002507.4(NGFR):c.395C>T (p.Ser132Leu)	not provided [RCV000898324]	benign	17	49506485	49506485	Human		name
155976325	CV2342761	single nucleotide variant	NM_002507.4(NGFR):c.1184G>C (p.Ser395Thr)	not specified [RCV004189805]	uncertain significance	17	49512909	49512909	Human		name
155932212	CV2364354	single nucleotide variant	NM_002507.4(NGFR):c.1198G>A (p.Ala400Thr)	not specified [RCV004223572]	uncertain significance	17	49512923	49512923	Human		name
401876918	CV2764215	single nucleotide variant	NM_002507.4(NGFR):c.1151G>A (p.Arg384His)	not specified [RCV004336757]	uncertain significance	17	49512876	49512876	Human		name
401892242	CV2776021	single nucleotide variant	NM_002507.4(NGFR):c.1197C>G (p.Asp399Glu)	not specified [RCV004353131]	uncertain significance	17	49512922	49512922	Human		name
407496992	CV3451305	single nucleotide variant	NM_002507.4(NGFR):c.1216C>T (p.Arg406Cys)	not specified [RCV004643639]	uncertain significance	17	49512941	49512941	Human		name
597657349	CV3559216	single nucleotide variant	NM_002507.4(NGFR):c.1018C>T (p.Pro340Ser)	not specified [RCV004834382]	uncertain significance	17	49512743	49512743	Human		name
597657282	CV3559226	single nucleotide variant	NM_002507.4(NGFR):c.1217G>A (p.Arg406His)	not specified [RCV004834392]	uncertain significance	17	49512942	49512942	Human		name
598192560	CV3997762	single nucleotide variant	NM_002507.4(NGFR):c.1057G>A (p.Gly353Ser)	not specified [RCV005374372]	uncertain significance	17	49512782	49512782	Human		name
598192576	CV3997766	single nucleotide variant	NM_002507.4(NGFR):c.1223T>C (p.Ile408Thr)	not specified [RCV005374375]	uncertain significance	17	49512948	49512948	Human		name

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