Jund Variant Search Result - Rat Genome Database

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41 records found for search term Jund

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401928610	CV2811847	single nucleotide variant	NM_005354.6(JUND):c.267C>T (p.Ala89=)	not provided [RCV003406905]	likely benign	19	18281218	18281218	Human		name
156329562	CV2213855	single nucleotide variant	NM_005354.6(JUND):c.76G>C (p.Ala26Pro)	not specified [RCV004089906]	uncertain significance	19	18281409	18281409	Human		name
156077612	CV2291661	single nucleotide variant	NM_005354.6(JUND):c.91T>G (p.Leu31Val)	not specified [RCV004155947]	uncertain significance	19	18281394	18281394	Human		name
407467239	CV3448207	single nucleotide variant	NM_005354.6(JUND):c.59G>T (p.Gly20Val)	not specified [RCV004635839]	uncertain significance	19	18281426	18281426	Human		name
15166823	CV741725	single nucleotide variant	NM_005354.6(JUND):c.825G>T (p.Arg275=)	not provided [RCV000904525]	benign	19	18280660	18280660	Human		name
15169446	CV741726	single nucleotide variant	NM_005354.6(JUND):c.589C>T (p.Leu197=)	not provided [RCV000905059]	likely benign	19	18280896	18280896	Human		name
156367833	CV2203597	single nucleotide variant	NM_005354.6(JUND):c.112A>C (p.Thr38Pro)	not specified [RCV004072788]	uncertain significance	19	18281373	18281373	Human		name
156072946	CV2240602	single nucleotide variant	NM_005354.6(JUND):c.158G>A (p.Ser53Asn)	not specified [RCV004119248]	uncertain significance	19	18281327	18281327	Human		name
155913052	CV2341697	single nucleotide variant	NM_005354.6(JUND):c.250C>T (p.Pro84Ser)	not specified [RCV004182616]	uncertain significance	19	18281235	18281235	Human		name
401865377	CV2755533	single nucleotide variant	NM_005354.6(JUND):c.215C>A (p.Pro72His)	not specified [RCV004340115]	uncertain significance	19	18281270	18281270	Human		name
405801525	CV3271775	single nucleotide variant	NM_005354.6(JUND):c.206C>T (p.Pro69Leu)	not specified [RCV004403473]	uncertain significance	19	18281279	18281279	Human		name
407467243	CV3448208	single nucleotide variant	NM_005354.6(JUND):c.212C>T (p.Thr71Ile)	not specified [RCV004635840]	uncertain significance	19	18281273	18281273	Human		name
597778050	CV3691520	single nucleotide variant	NM_005354.6(JUND):c.256G>C (p.Gly86Arg)	not specified [RCV004930039]	uncertain significance	19	18281229	18281229	Human		name
598233855	CV3979855	single nucleotide variant	NM_005354.6(JUND):c.141G>C (p.Lys47Asn)	not specified [RCV005363421]	uncertain significance	19	18281344	18281344	Human		name
598233860	CV3979857	single nucleotide variant	NM_005354.6(JUND):c.245C>T (p.Ala82Val)	not specified [RCV005363422]	uncertain significance	19	18281240	18281240	Human		name
155962615	CV2197608	single nucleotide variant	NM_005354.6(JUND):c.488C>G (p.Ala163Gly)	not specified [RCV004074825]	uncertain significance	19	18280997	18280997	Human		name
156208102	CV2360505	single nucleotide variant	NM_005354.6(JUND):c.807C>G (p.Ile269Met)	not specified [RCV004210869]	uncertain significance	19	18280678	18280678	Human		name
156384731	CV2371575	single nucleotide variant	NM_005354.6(JUND):c.611C>T (p.Ala204Val)	not specified [RCV004216823]	uncertain significance	19	18280874	18280874	Human		name
329366374	CV2445688	single nucleotide variant	NM_005354.6(JUND):c.532C>T (p.Pro178Ser)	not specified [RCV004259762]	uncertain significance	19	18280953	18280953	Human		name
401720538	CV2673367	single nucleotide variant	NM_005354.6(JUND):c.860A>G (p.Lys287Arg)	not specified [RCV004288348]	uncertain significance	19	18280625	18280625	Human		name
401731371	CV2693756	single nucleotide variant	NM_005354.6(JUND):c.614G>A (p.Gly205Glu)	not specified [RCV004298080]	uncertain significance	19	18280871	18280871	Human		name
401887307	CV2773311	single nucleotide variant	NM_005354.6(JUND):c.443A>C (p.His148Pro)	not specified [RCV004353976]	uncertain significance	19	18281042	18281042	Human		name
405801527	CV3271776	single nucleotide variant	NM_005354.6(JUND):c.476C>G (p.Ala159Gly)	not specified [RCV004403474]	uncertain significance	19	18281009	18281009	Human		name
405801529	CV3271777	single nucleotide variant	NM_005354.6(JUND):c.481G>A (p.Ala161Thr)	not specified [RCV004403475]	uncertain significance	19	18281004	18281004	Human		name
405801533	CV3271779	single nucleotide variant	NM_005354.6(JUND):c.514A>G (p.Thr172Ala)	not specified [RCV004403477]	uncertain significance	19	18280971	18280971	Human		name
405801535	CV3271780	single nucleotide variant	NM_005354.6(JUND):c.515C>T (p.Thr172Met)	not specified [RCV004403478]	uncertain significance	19	18280970	18280970	Human		name
405801537	CV3271781	single nucleotide variant	NM_005354.6(JUND):c.682C>G (p.Pro228Ala)	not specified [RCV004403479]	uncertain significance	19	18280803	18280803	Human		name
405801541	CV3271783	single nucleotide variant	NM_005354.6(JUND):c.938C>T (p.Thr313Met)	not specified [RCV004403481]	uncertain significance	19	18280547	18280547	Human		name
405801543	CV3271784	single nucleotide variant	NM_005354.6(JUND):c.977A>G (p.Gln326Arg)	not specified [RCV004403482]	uncertain significance	19	18280508	18280508	Human		name
407467235	CV3448206	single nucleotide variant	NM_005354.6(JUND):c.361T>A (p.Ser121Thr)	not specified [RCV004635838]	likely benign	19	18281124	18281124	Human		name
407511655	CV3448209	single nucleotide variant	NM_005354.6(JUND):c.646G>C (p.Ala216Pro)	not specified [RCV004626534]	uncertain significance	19	18280839	18280839	Human		name
407511658	CV3448210	single nucleotide variant	NM_005354.6(JUND):c.647C>T (p.Ala216Val)	not specified [RCV004626535]	uncertain significance	19	18280838	18280838	Human		name
597778057	CV3691521	single nucleotide variant	NM_005354.6(JUND):c.512G>C (p.Gly171Ala)	not specified [RCV004930040]	uncertain significance	19	18280973	18280973	Human		name
597778061	CV3691522	single nucleotide variant	NM_005354.6(JUND):c.414G>C (p.Glu138Asp)	not specified [RCV004930041]	uncertain significance	19	18281071	18281071	Human		name
597778069	CV3691524	single nucleotide variant	NM_005354.6(JUND):c.599A>G (p.Tyr200Cys)	not specified [RCV004930043]	uncertain significance	19	18280886	18280886	Human		name
597778076	CV3691525	single nucleotide variant	NM_005354.6(JUND):c.668C>T (p.Pro223Leu)	not specified [RCV004930044]	uncertain significance	19	18280817	18280817	Human		name
597778080	CV3691526	single nucleotide variant	NM_005354.6(JUND):c.565C>G (p.Pro189Ala)	not specified [RCV004930045]	uncertain significance	19	18280920	18280920	Human		name
598212311	CV3979856	single nucleotide variant	NM_005354.6(JUND):c.703C>T (p.Arg235Cys)	not specified [RCV005358808]	uncertain significance	19	18280782	18280782	Human		name
156270053	CV2305953	single nucleotide variant	NM_005354.6(JUND):c.1027C>G (p.Gln343Glu)	not specified [RCV004167731]	uncertain significance	19	18280458	18280458	Human		name
598233847	CV3979853	single nucleotide variant	NM_005354.6(JUND):c.1016T>C (p.Leu339Pro)	not specified [RCV005363420]	uncertain significance	19	18280469	18280469	Human		name
598258910	CV3979854	single nucleotide variant	NM_005354.6(JUND):c.1033C>T (p.Pro345Ser)	not specified [RCV005347304]	uncertain significance	19	18280452	18280452	Human		name

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