Igf2bp3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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40 records found for search term Igf2bp3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15190295	CV777654	single nucleotide variant	NM_006547.3(IGF2BP3):c.1204-7C>A	not provided [RCV000954433]	benign	7	23319261	23319261	Human		name
8590731	CV125440	single nucleotide variant	NM_006547.2(IGF2BP3):c.237-4614A>G	Lung cancer [RCV000105959]	uncertain significance	7	23423438	23423438	Human		name
153000031	CV1683583	single nucleotide variant	NM_006547.3(IGF2BP3):c.285+21968C>T	Vascular endothelial growth factor (VEGF) inhibitor response [RCV002254038]	association	7	23396808	23396808	Human		name
8632526	CV87734	single nucleotide variant	NM_006547.2(IGF2BP3):c.19G>C (p.Gly7Arg)	Malignant melanoma [RCV000067826]	not provided	7	23470092	23470092	Human		name
8590732	CV125441	single nucleotide variant	NM_006547.2(IGF2BP3):c.235A>T (p.Arg79Trp)	Lung cancer [RCV000105960]	uncertain significance	7	23468483	23468483	Human		name
155978983	CV2222785	single nucleotide variant	NM_006547.3(IGF2BP3):c.134C>T (p.Pro45Leu)	not specified [RCV004101625]	uncertain significance	7	23469977	23469977	Human		name
329353712	CV2439573	single nucleotide variant	NM_006547.3(IGF2BP3):c.202A>G (p.Ile68Val)	not specified [RCV004255596]	uncertain significance	7	23468516	23468516	Human		name
401735437	CV2672652	single nucleotide variant	NM_006547.3(IGF2BP3):c.269C>G (p.Pro90Arg)	not specified [RCV004287673]	uncertain significance	7	23418792	23418792	Human		name
401780201	CV2673915	single nucleotide variant	NM_006547.3(IGF2BP3):c.139G>A (p.Glu47Lys)	not specified [RCV004293289]	uncertain significance	7	23469972	23469972	Human		name
401732049	CV2677982	single nucleotide variant	NM_006547.3(IGF2BP3):c.250C>G (p.Gln84Glu)	not specified [RCV004296512]	uncertain significance	7	23418811	23418811	Human		name
405799384	CV3263981	single nucleotide variant	NM_006547.3(IGF2BP3):c.244A>C (p.Lys82Gln)	not specified [RCV004402433]	uncertain significance	7	23418817	23418817	Human		name
407515103	CV3440734	single nucleotide variant	NM_006547.3(IGF2BP3):c.133C>G (p.Pro45Ala)	not specified [RCV004627726]	uncertain significance	7	23469978	23469978	Human		name
156309496	CV2249644	single nucleotide variant	NM_006547.3(IGF2BP3):c.861T>G (p.Phe287Leu)	not specified [RCV004120648]	uncertain significance	7	23346020	23346020	Human		name
156031555	CV2249829	single nucleotide variant	NM_006547.3(IGF2BP3):c.610A>G (p.Thr204Ala)	not specified [RCV004122578]	uncertain significance	7	23351378	23351378	Human		name
156267490	CV2296649	single nucleotide variant	NM_006547.3(IGF2BP3):c.698G>A (p.Arg233His)	not specified [RCV004154703]	uncertain significance	7	23347720	23347720	Human		name
156306834	CV2312086	single nucleotide variant	NM_006547.3(IGF2BP3):c.920A>G (p.Asp307Gly)	not specified [RCV004165009]	uncertain significance	7	23345961	23345961	Human		name
156334843	CV2333445	single nucleotide variant	NM_006547.3(IGF2BP3):c.710C>T (p.Ala237Val)	not specified [RCV004190148]	uncertain significance	7	23347708	23347708	Human		name
156080368	CV2384631	single nucleotide variant	NM_006547.3(IGF2BP3):c.562G>A (p.Val188Ile)	not specified [RCV004232413]	uncertain significance	7	23351426	23351426	Human		name
329384530	CV2435099	single nucleotide variant	NM_006547.3(IGF2BP3):c.517G>T (p.Gly173Trp)	not specified [RCV004252744]	uncertain significance	7	23351471	23351471	Human		name
329364838	CV2443956	single nucleotide variant	NM_006547.3(IGF2BP3):c.911A>G (p.Gln304Arg)	not specified [RCV004258284]	uncertain significance	7	23345970	23345970	Human		name
329370637	CV2461789	single nucleotide variant	NM_006547.3(IGF2BP3):c.773A>G (p.Lys258Arg)	not specified [RCV004271715]	uncertain significance	7	23347645	23347645	Human		name
405799379	CV3263982	single nucleotide variant	NM_006547.3(IGF2BP3):c.512G>A (p.Arg171His)	not specified [RCV004402434]	uncertain significance	7	23351476	23351476	Human		name
407515111	CV3440732	single nucleotide variant	NM_006547.3(IGF2BP3):c.536C>T (p.Ser179Phe)	not specified [RCV004627724]	uncertain significance	7	23351452	23351452	Human		name
407515106	CV3440733	single nucleotide variant	NM_006547.3(IGF2BP3):c.460A>G (p.Ile154Val)	not specified [RCV004627725]	uncertain significance	7	23351528	23351528	Human		name
407511098	CV3440736	single nucleotide variant	NM_006547.3(IGF2BP3):c.419A>G (p.Asn140Ser)	not specified [RCV004626352]	uncertain significance	7	23351569	23351569	Human		name
598268862	CV3975657	single nucleotide variant	NM_006547.3(IGF2BP3):c.309G>T (p.Gln103His)	not specified [RCV005349791]	uncertain significance	7	23361718	23361718	Human		name
598268867	CV3975658	single nucleotide variant	NM_006547.3(IGF2BP3):c.362T>C (p.Val121Ala)	not specified [RCV005349792]	uncertain significance	7	23361573	23361573	Human		name
598268875	CV3975659	single nucleotide variant	NM_006547.3(IGF2BP3):c.604G>A (p.Val202Ile)	not specified [RCV005349793]	uncertain significance	7	23351384	23351384	Human		name
8632525	CV87733	single nucleotide variant	NM_006547.2(IGF2BP3):c.352G>A (p.Glu118Lys)	Malignant melanoma [RCV000067825]	not provided	7	23361583	23361583	Human		name
127328399	CV985501	single nucleotide variant	NM_006547.3(IGF2BP3):c.922A>G (p.Thr308Ala)	Primary microcephaly [RCV001786463]	uncertain significance	7	23345959	23345959	Human	2	name
156160430	CV2262664	single nucleotide variant	NM_006547.3(IGF2BP3):c.1021G>A (p.Glu341Lys)	not specified [RCV004130859]	uncertain significance	7	23343774	23343774	Human		name
156166519	CV2330135	single nucleotide variant	NM_006547.3(IGF2BP3):c.1564G>A (p.Val522Ile)	not specified [RCV004185625]	uncertain significance	7	23312812	23312812	Human		name
156197861	CV2357743	single nucleotide variant	NM_006547.3(IGF2BP3):c.1193C>T (p.Pro398Leu)	not specified [RCV004205037]	uncertain significance	7	23342074	23342074	Human		name
155998984	CV2373365	single nucleotide variant	NM_006547.3(IGF2BP3):c.1526C>T (p.Thr509Met)	not specified [RCV004220072]	uncertain significance	7	23313523	23313523	Human		name
405799390	CV3263980	single nucleotide variant	NM_006547.3(IGF2BP3):c.1113C>G (p.Asn371Lys)	not specified [RCV004402432]	uncertain significance	7	23342154	23342154	Human		name
407515100	CV3440735	single nucleotide variant	NM_006547.3(IGF2BP3):c.1183C>T (p.Pro395Ser)	not specified [RCV004627727]	uncertain significance	7	23342084	23342084	Human		name
597764379	CV3680094	single nucleotide variant	NM_006547.3(IGF2BP3):c.1088A>C (p.His363Pro)	not specified [RCV004926578]	uncertain significance	7	23342179	23342179	Human		name
597764605	CV3680095	single nucleotide variant	NM_006547.3(IGF2BP3):c.1174G>A (p.Ala392Thr)	not specified [RCV004926579]	uncertain significance	7	23342093	23342093	Human		name
598206852	CV3975656	single nucleotide variant	NM_006547.3(IGF2BP3):c.1717C>G (p.Pro573Ala)	not specified [RCV005337867]	uncertain significance	7	23312385	23312385	Human		name
8632524	CV87732	single nucleotide variant	NM_006547.2(IGF2BP3):c.1193C>G (p.Pro398Arg)	Malignant melanoma [RCV000067824]	not provided	7	23342074	23342074	Human		name

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