Nob1 Variant Search Result - Rat Genome Database

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55 records found for search term Nob1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15161652	CV703784	single nucleotide variant	NM_014062.3(NOB1):c.43C>T (p.Leu15=)	not provided [RCV000947711]	benign	16	69754868	69754868	Human		name
407497939	CV3458929	single nucleotide variant	NM_014062.3(NOB1):c.26C>T (p.Ala9Val)	not specified [RCV004643877]	uncertain significance	16	69754885	69754885	Human		name
597671149	CV3566362	single nucleotide variant	NM_014062.3(NOB1):c.16C>T (p.His6Tyr)	not specified [RCV004829769]	uncertain significance	16	69754895	69754895	Human		name
15175277	CV715034	single nucleotide variant	NM_014062.3(NOB1):c.264A>T (p.Ala88=)	not provided [RCV000972906]	likely benign	16	69752304	69752304	Human		name
156314349	CV2196633	single nucleotide variant	NM_014062.3(NOB1):c.229C>T (p.Pro77Ser)	not specified [RCV004073900]	uncertain significance	16	69752339	69752339	Human		name
401783206	CV2716179	single nucleotide variant	NM_014062.3(NOB1):c.152A>G (p.Tyr51Cys)	not specified [RCV004323411]	uncertain significance	16	69754638	69754638	Human		name
405725986	CV3355327	single nucleotide variant	NM_014062.3(NOB1):c.171G>T (p.Glu57Asp)	not specified [RCV004495793]	uncertain significance	16	69754619	69754619	Human		name
405725997	CV3355328	single nucleotide variant	NM_014062.3(NOB1):c.272A>G (p.Tyr91Cys)	not specified [RCV004495794]	uncertain significance	16	69752296	69752296	Human		name
407509496	CV3458928	single nucleotide variant	NM_014062.3(NOB1):c.173C>T (p.Pro58Leu)	not specified [RCV004647434]	uncertain significance	16	69754617	69754617	Human		name
156269440	CV2240135	single nucleotide variant	NM_014062.3(NOB1):c.494C>G (p.Pro165Arg)	not specified [RCV004110897]	uncertain significance	16	69749244	69749244	Human		name
156253296	CV2264567	single nucleotide variant	NM_014062.3(NOB1):c.787G>A (p.Ala263Thr)	not specified [RCV004132581]	uncertain significance	16	69748269	69748269	Human		name
156104577	CV2291742	single nucleotide variant	NM_014062.3(NOB1):c.804G>T (p.Leu268Phe)	not specified [RCV004158021]	uncertain significance	16	69748252	69748252	Human		name
156092794	CV2300166	single nucleotide variant	NM_014062.3(NOB1):c.418A>G (p.Thr140Ala)	not specified [RCV004151355]	uncertain significance	16	69749320	69749320	Human		name
156095618	CV2310121	single nucleotide variant	NM_014062.3(NOB1):c.910G>A (p.Gly304Ser)	not specified [RCV004163243]	uncertain significance	16	69744932	69744932	Human		name
156273514	CV2323693	single nucleotide variant	NM_014062.3(NOB1):c.856T>C (p.Ser286Pro)	not specified [RCV004165869]	uncertain significance	16	69744986	69744986	Human		name
156285401	CV2334839	single nucleotide variant	NM_014062.3(NOB1):c.935G>C (p.Arg312Pro)	not specified [RCV004181949]	uncertain significance	16	69744907	69744907	Human		name
156082830	CV2394834	single nucleotide variant	NM_014062.3(NOB1):c.971A>T (p.Tyr324Phe)	not specified [RCV004234496]	uncertain significance	16	69742600	69742600	Human		name
329361658	CV2437744	single nucleotide variant	NM_014062.3(NOB1):c.697G>C (p.Gly233Arg)	not specified [RCV004261048]	uncertain significance	16	69748947	69748947	Human		name
329358683	CV2450663	single nucleotide variant	NM_014062.3(NOB1):c.370C>T (p.His124Tyr)	not specified [RCV004265829]	uncertain significance	16	69749588	69749588	Human		name
401742605	CV2673826	single nucleotide variant	NM_014062.3(NOB1):c.694G>A (p.Val232Ile)	not specified [RCV004293209]	uncertain significance	16	69748950	69748950	Human		name
401766497	CV2679716	single nucleotide variant	NM_014062.3(NOB1):c.528T>G (p.Ile176Met)	not specified [RCV004282186]	uncertain significance	16	69749116	69749116	Human		name
401731576	CV2701433	single nucleotide variant	NM_014062.3(NOB1):c.823A>G (p.Lys275Glu)	not specified [RCV004311789]	uncertain significance	16	69748233	69748233	Human		name
401855933	CV2754124	single nucleotide variant	NM_014062.3(NOB1):c.600C>G (p.Asp200Glu)	not specified [RCV004334320]	uncertain significance	16	69749044	69749044	Human		name
401898063	CV2780132	single nucleotide variant	NM_014062.3(NOB1):c.682G>A (p.Glu228Lys)	not specified [RCV004355789]	likely benign	16	69748962	69748962	Human		name
401875871	CV2789193	single nucleotide variant	NM_014062.3(NOB1):c.614G>A (p.Gly205Glu)	not specified [RCV004365235]	uncertain significance	16	69749030	69749030	Human		name
405726025	CV3355331	single nucleotide variant	NM_014062.3(NOB1):c.319C>T (p.Pro107Ser)	not specified [RCV004495797]	uncertain significance	16	69752249	69752249	Human		name
405726032	CV3355332	single nucleotide variant	NM_014062.3(NOB1):c.613G>A (p.Gly205Arg)	not specified [RCV004495798]	uncertain significance	16	69749031	69749031	Human		name
405726043	CV3355333	single nucleotide variant	NM_014062.3(NOB1):c.715T>C (p.Phe239Leu)	not specified [RCV004495799]	uncertain significance	16	69748929	69748929	Human		name
405726051	CV3355334	single nucleotide variant	NM_014062.3(NOB1):c.769G>A (p.Gly257Ser)	not specified [RCV004495800]	uncertain significance	16	69748287	69748287	Human		name
405726059	CV3355335	single nucleotide variant	NM_014062.3(NOB1):c.782G>A (p.Arg261His)	not specified [RCV004495801]	uncertain significance	16	69748274	69748274	Human		name
405726070	CV3355336	single nucleotide variant	NM_014062.3(NOB1):c.967C>T (p.Arg323Trp)	not specified [RCV004495802]	uncertain significance	16	69744875	69744875	Human		name
407497943	CV3458930	single nucleotide variant	NM_014062.3(NOB1):c.718G>A (p.Ala240Thr)	not specified [RCV004643878]	uncertain significance	16	69748926	69748926	Human		name
407497947	CV3458931	single nucleotide variant	NM_014062.3(NOB1):c.298G>A (p.Val100Met)	not specified [RCV004643879]	uncertain significance	16	69752270	69752270	Human		name
597671140	CV3566361	single nucleotide variant	NM_014062.3(NOB1):c.407C>T (p.Pro136Leu)	not specified [RCV004829768]	uncertain significance	16	69749331	69749331	Human		name
597671160	CV3566363	single nucleotide variant	NM_014062.3(NOB1):c.881A>G (p.Lys294Arg)	not specified [RCV004829770]	uncertain significance	16	69744961	69744961	Human		name
597671167	CV3566364	single nucleotide variant	NM_014062.3(NOB1):c.914C>T (p.Thr305Ile)	not specified [RCV004829771]	uncertain significance	16	69744928	69744928	Human		name
597671184	CV3566366	single nucleotide variant	NM_014062.3(NOB1):c.347T>G (p.Ile116Ser)	not specified [RCV004829773]	uncertain significance	16	69749611	69749611	Human		name
597671192	CV3566367	single nucleotide variant	NM_014062.3(NOB1):c.644A>G (p.Lys215Arg)	not specified [RCV004829774]	uncertain significance	16	69749000	69749000	Human		name
598206445	CV4004423	single nucleotide variant	NM_014062.3(NOB1):c.344C>T (p.Ser115Leu)	not specified [RCV005376922]	uncertain significance	16	69749614	69749614	Human		name
598239843	CV4004425	single nucleotide variant	NM_014062.3(NOB1):c.723G>T (p.Met241Ile)	not specified [RCV005383000]	uncertain significance	16	69748921	69748921	Human		name
598206460	CV4004427	single nucleotide variant	NM_014062.3(NOB1):c.604G>A (p.Asp202Asn)	not specified [RCV005376925]	uncertain significance	16	69749040	69749040	Human		name
155914531	CV2342021	single nucleotide variant	NM_014062.3(NOB1):c.1086C>A (p.Phe362Leu)	not specified [RCV004184958]	uncertain significance	16	69742485	69742485	Human		name
156179494	CV2374676	single nucleotide variant	NM_014062.3(NOB1):c.1087G>A (p.Ala363Thr)	not specified [RCV004225291]	uncertain significance	16	69742484	69742484	Human		name
401759960	CV2701807	single nucleotide variant	NM_014062.3(NOB1):c.1095C>A (p.Asp365Glu)	not specified [RCV004314197]	uncertain significance	16	69742476	69742476	Human		name
405725978	CV3355326	single nucleotide variant	NM_014062.3(NOB1):c.1141C>T (p.Arg381Cys)	not specified [RCV004495792]	uncertain significance	16	69742430	69742430	Human		name
407509503	CV3458933	single nucleotide variant	NM_014062.3(NOB1):c.1024G>A (p.Glu342Lys)	not specified [RCV004647436]	uncertain significance	16	69742547	69742547	Human		name
407509507	CV3458934	single nucleotide variant	NM_014062.3(NOB1):c.1025A>C (p.Glu342Ala)	not specified [RCV004647437]	uncertain significance	16	69742546	69742546	Human		name
597671125	CV3566359	single nucleotide variant	NM_014062.3(NOB1):c.1193G>A (p.Arg398His)	not specified [RCV004829766]	uncertain significance	16	69742378	69742378	Human		name
597671132	CV3566360	single nucleotide variant	NM_014062.3(NOB1):c.1003G>A (p.Ala335Thr)	not specified [RCV004829767]	uncertain significance	16	69742568	69742568	Human		name
597671176	CV3566365	single nucleotide variant	NM_014062.3(NOB1):c.1105G>A (p.Gly369Arg)	not specified [RCV004829772]	uncertain significance	16	69742466	69742466	Human		name
597671201	CV3566368	single nucleotide variant	NM_014062.3(NOB1):c.1162C>T (p.Arg388Trp)	not specified [RCV004829775]	uncertain significance	16	69742409	69742409	Human		name
597671209	CV3566369	single nucleotide variant	NM_014062.3(NOB1):c.1121T>C (p.Val374Ala)	not specified [RCV004829776]	likely benign	16	69742450	69742450	Human		name
597671216	CV3566370	single nucleotide variant	NM_014062.3(NOB1):c.1184G>A (p.Gly395Glu)	not specified [RCV004829777]	uncertain significance	16	69742387	69742387	Human		name
598206450	CV4004424	single nucleotide variant	NM_014062.3(NOB1):c.1177G>A (p.Gly393Arg)	not specified [RCV005376923]	uncertain significance	16	69742394	69742394	Human		name
598206454	CV4004426	single nucleotide variant	NM_014062.3(NOB1):c.1061A>T (p.Lys354Met)	not specified [RCV005376924]	uncertain significance	16	69742510	69742510	Human		name

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