Igf2bp2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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37 records found for search term Igf2bp2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8595773	CV17474	single nucleotide variant	NM_006548.6(IGF2BP2):c.239+29254C>A	Diabetes mellitus type 2, susceptibility to [RCV000002537]	risk factor	3	185793899	185793899	Human	5	name
8595773	CV17474	single nucleotide variant	NM_006548.6(IGF2BP2):c.239+29254C>A	Diabetes mellitus type 2, susceptibility to [RCV000002537]	risk factor	3	185793899	185793900	Human	5	name
156051898	CV2336696	single nucleotide variant	NM_006548.6(IGF2BP2):c.46G>A (p.Ala16Thr)	not specified [RCV004196936]	uncertain significance	3	185824915	185824915	Human		name
597764359	CV3680089	single nucleotide variant	NM_006548.6(IGF2BP2):c.92C>A (p.Ala31Glu)	not specified [RCV004926573]	uncertain significance	3	185824869	185824869	Human		name
598206842	CV3975650	single nucleotide variant	NM_006548.6(IGF2BP2):c.118T>C (p.Tyr40His)	not specified [RCV005337865]	uncertain significance	3	185824843	185824843	Human		name
598268845	CV3975653	single nucleotide variant	NM_006548.6(IGF2BP2):c.172C>A (p.Leu58Ile)	not specified [RCV005349788]	uncertain significance	3	185824789	185824789	Human		name
598268851	CV3975654	single nucleotide variant	NM_006548.6(IGF2BP2):c.221C>T (p.Ser74Leu)	not specified [RCV005349789]	uncertain significance	3	185823171	185823171	Human		name
15140115	CV748143	single nucleotide variant	NM_006548.6(IGF2BP2):c.1443A>T (p.Pro481=)	not provided [RCV000921625]	likely benign	3	185652112	185652112	Human		name
156330150	CV2216574	single nucleotide variant	NM_006548.6(IGF2BP2):c.530G>A (p.Arg177Gln)	not specified [RCV004097341]	uncertain significance	3	185689502	185689502	Human		name
156129305	CV2364622	single nucleotide variant	NM_006548.6(IGF2BP2):c.442T>C (p.Tyr148His)	not specified [RCV004219514]	uncertain significance	3	185689590	185689590	Human		name
401728821	CV2673058	single nucleotide variant	NM_006548.6(IGF2BP2):c.364G>A (p.Val122Ile)	not specified [RCV004284046]	uncertain significance	3	185692739	185692739	Human		name
401739402	CV2673280	single nucleotide variant	NM_006548.6(IGF2BP2):c.488C>T (p.Pro163Leu)	not specified [RCV004286081]	uncertain significance	3	185689544	185689544	Human		name
405799400	CV3263977	single nucleotide variant	NM_006548.6(IGF2BP2):c.461A>G (p.Tyr154Cys)	not specified [RCV004402429]	uncertain significance	3	185689571	185689571	Human		name
405799397	CV3263978	single nucleotide variant	NM_006548.6(IGF2BP2):c.671A>G (p.Gln224Arg)	not specified [RCV004402430]	uncertain significance	3	185689361	185689361	Human		name
405799393	CV3263979	single nucleotide variant	NM_006548.6(IGF2BP2):c.928A>G (p.Ile310Val)	not specified [RCV004402431]	uncertain significance	3	185675798	185675798	Human		name
597764344	CV3680085	single nucleotide variant	NM_006548.6(IGF2BP2):c.424G>A (p.Gly142Arg)	not specified [RCV004926569]	uncertain significance	3	185689608	185689608	Human		name
597764347	CV3680086	single nucleotide variant	NM_006548.6(IGF2BP2):c.954A>G (p.Ile318Met)	not specified [RCV004926570]	uncertain significance	3	185675413	185675413	Human		name
597764367	CV3680091	single nucleotide variant	NM_006548.6(IGF2BP2):c.612T>G (p.Phe204Leu)	not specified [RCV004926575]	uncertain significance	3	185689420	185689420	Human		name
597764371	CV3680092	single nucleotide variant	NM_006548.6(IGF2BP2):c.898A>G (p.Ile300Val)	not specified [RCV004926576]	uncertain significance	3	185675828	185675828	Human		name
597764375	CV3680093	single nucleotide variant	NM_006548.6(IGF2BP2):c.308C>T (p.Ala103Val)	not specified [RCV004926577]	uncertain significance	3	185696644	185696644	Human		name
156186548	CV2232666	single nucleotide variant	NM_006548.6(IGF2BP2):c.1717C>T (p.Arg573Cys)	not specified [RCV004101334]	uncertain significance	3	185645614	185645614	Human		name
329385693	CV2432192	single nucleotide variant	NM_006548.6(IGF2BP2):c.1306A>T (p.Thr436Ser)	not specified [RCV004249333]	uncertain significance	3	185657366	185657366	Human		name
329400078	CV2440532	single nucleotide variant	NM_006548.6(IGF2BP2):c.1181C>T (p.Ala394Val)	not specified [RCV004256449]	uncertain significance	3	185672560	185672560	Human		name
329396404	CV2459630	single nucleotide variant	NM_006548.6(IGF2BP2):c.1208C>T (p.Ser403Phe)	not specified [RCV004277069]	uncertain significance	3	185658402	185658402	Human		name
401862313	CV2775219	single nucleotide variant	NM_006548.6(IGF2BP2):c.1162C>T (p.Arg388Cys)	not specified [RCV004348351]	uncertain significance	3	185672579	185672579	Human		name
405799414	CV3263972	single nucleotide variant	NM_006548.6(IGF2BP2):c.1015A>G (p.Ile339Val)	not specified [RCV004402424]	likely benign	3	185675352	185675352	Human		name
405799411	CV3263973	single nucleotide variant	NM_006548.6(IGF2BP2):c.1081A>T (p.Asn361Tyr)	not specified [RCV004402425]	uncertain significance	3	185672660	185672660	Human		name
405799408	CV3263974	single nucleotide variant	NM_006548.6(IGF2BP2):c.1106G>A (p.Ser369Asn)	not specified [RCV004402426]	uncertain significance	3	185672635	185672635	Human		name
405799405	CV3263975	single nucleotide variant	NM_006548.6(IGF2BP2):c.1138G>A (p.Val380Met)	not specified [RCV004402427]	uncertain significance	3	185672603	185672603	Human		name
405799402	CV3263976	single nucleotide variant	NM_006548.6(IGF2BP2):c.1171C>T (p.Pro391Ser)	not specified [RCV004402428]	uncertain significance	3	185672570	185672570	Human		name
407515115	CV3440731	single nucleotide variant	NM_006548.6(IGF2BP2):c.1535C>T (p.Ala512Val)	not specified [RCV004627723]	uncertain significance	3	185649461	185649461	Human		name
596938247	CV3550051	single nucleotide variant	NM_006548.6(IGF2BP2):c.1718G>T (p.Arg573Leu)	Familial juvenile hyperuricemic nephropathy type 1 [RCV004813356]	uncertain significance	3	185645613	185645613	Human	1	name
597764351	CV3680087	single nucleotide variant	NM_006548.6(IGF2BP2):c.1665G>C (p.Glu555Asp)	not specified [RCV004926571]	uncertain significance	3	185647067	185647067	Human		name
597764355	CV3680088	single nucleotide variant	NM_006548.6(IGF2BP2):c.1321G>A (p.Ala441Thr)	not specified [RCV004926572]	uncertain significance	3	185657351	185657351	Human		name
598206847	CV3975651	single nucleotide variant	NM_006548.6(IGF2BP2):c.1037G>A (p.Arg346His)	not specified [RCV005337866]	uncertain significance	3	185675330	185675330	Human		name
598268840	CV3975652	single nucleotide variant	NM_006548.6(IGF2BP2):c.1458C>A (p.Phe486Leu)	not specified [RCV005349787]	uncertain significance	3	185652097	185652097	Human		name
598268857	CV3975655	single nucleotide variant	NM_006548.6(IGF2BP2):c.1790G>T (p.Arg597Leu)	not specified [RCV005349790]	uncertain significance	3	185645541	185645541	Human		name

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