Imp4 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 Imp4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329379059	CV2460130	single nucleotide variant	NM_033416.3(IMP4):c.62C>T (p.Ala21Val)	not specified [RCV004273236]	uncertain significance	2	130343144	130343144	Human		name
407516273	CV3444699	single nucleotide variant	NM_033416.3(IMP4):c.84G>C (p.Arg28Ser)	not specified [RCV004628139]	uncertain significance	2	130343166	130343166	Human		name
407516279	CV3444701	single nucleotide variant	NM_033416.3(IMP4):c.68G>T (p.Arg23Leu)	not specified [RCV004628141]	uncertain significance	2	130343150	130343150	Human		name
156253249	CV2212531	single nucleotide variant	NM_033416.3(IMP4):c.143G>A (p.Arg48Gln)	not specified [RCV004091414]	uncertain significance	2	130344659	130344659	Human		name
405782522	CV3267518	single nucleotide variant	NM_033416.3(IMP4):c.116A>G (p.Asn39Ser)	not specified [RCV004397892]	uncertain significance	2	130344632	130344632	Human		name
405782528	CV3267519	single nucleotide variant	NM_033416.3(IMP4):c.119G>A (p.Arg40His)	not specified [RCV004397893]	uncertain significance	2	130344635	130344635	Human		name
405782534	CV3267520	single nucleotide variant	NM_033416.3(IMP4):c.140G>A (p.Arg47His)	not specified [RCV004397894]	uncertain significance	2	130344656	130344656	Human		name
407516270	CV3444698	single nucleotide variant	NM_033416.3(IMP4):c.161A>G (p.Gln54Arg)	not specified [RCV004628138]	uncertain significance	2	130344677	130344677	Human		name
598180782	CV3972419	single nucleotide variant	NM_033416.3(IMP4):c.211G>A (p.Val71Met)	not specified [RCV005352388]	uncertain significance	2	130345390	130345390	Human		name
156081255	CV2195402	single nucleotide variant	NM_033416.3(IMP4):c.451G>A (p.Val151Ile)	not specified [RCV004080314]	uncertain significance	2	130345790	130345790	Human		name
156332618	CV2220713	single nucleotide variant	NM_033416.3(IMP4):c.749G>A (p.Arg250His)	not specified [RCV004097884]	uncertain significance	2	130346260	130346260	Human		name
156088080	CV2241373	single nucleotide variant	NM_033416.3(IMP4):c.639C>G (p.Asp213Glu)	not specified [RCV004102506]	uncertain significance	2	130346062	130346062	Human		name
156313232	CV2256985	single nucleotide variant	NM_033416.3(IMP4):c.823T>C (p.Trp275Arg)	not specified [RCV004121172]	uncertain significance	2	130346415	130346415	Human		name
156188376	CV2292539	single nucleotide variant	NM_033416.3(IMP4):c.739G>A (p.Val247Ile)	not specified [RCV004150312]	uncertain significance	2	130346250	130346250	Human		name
156298894	CV2310666	single nucleotide variant	NM_033416.3(IMP4):c.715C>G (p.His239Asp)	not specified [RCV004157326]	uncertain significance	2	130346226	130346226	Human		name
156290668	CV2342677	single nucleotide variant	NM_033416.3(IMP4):c.326C>T (p.Pro109Leu)	not specified [RCV004196759]	uncertain significance	2	130345586	130345586	Human		name
156345554	CV2356276	single nucleotide variant	NM_033416.3(IMP4):c.377G>A (p.Arg126Gln)	not specified [RCV004206086]	uncertain significance	2	130345637	130345637	Human		name
155907799	CV2387122	single nucleotide variant	NM_033416.3(IMP4):c.507G>A (p.Met169Ile)	not specified [RCV004238231]	uncertain significance	2	130345846	130345846	Human		name
329398352	CV2465039	single nucleotide variant	NM_033416.3(IMP4):c.403G>C (p.Asp135His)	not specified [RCV004286774]	uncertain significance	2	130345663	130345663	Human		name
401726843	CV2691866	single nucleotide variant	NM_033416.3(IMP4):c.748C>T (p.Arg250Cys)	not specified [RCV004299608]	uncertain significance	2	130346259	130346259	Human		name
401725455	CV2721783	single nucleotide variant	NM_033416.3(IMP4):c.820C>T (p.Arg274Cys)	not specified [RCV004326305]	uncertain significance	2	130346412	130346412	Human		name
401860571	CV2776102	single nucleotide variant	NM_033416.3(IMP4):c.647G>A (p.Arg216Gln)	not specified [RCV004353204]	uncertain significance	2	130346070	130346070	Human		name
401888250	CV2788197	single nucleotide variant	NM_033416.3(IMP4):c.452T>C (p.Val151Ala)	not specified [RCV004352810]	uncertain significance	2	130345791	130345791	Human		name
405782542	CV3267521	single nucleotide variant	NM_033416.3(IMP4):c.310C>G (p.Leu104Val)	not specified [RCV004397895]	uncertain significance	2	130345570	130345570	Human		name
405782548	CV3267522	single nucleotide variant	NM_033416.3(IMP4):c.473C>T (p.Pro158Leu)	not specified [RCV004397896]	uncertain significance	2	130345812	130345812	Human		name
405782554	CV3267523	single nucleotide variant	NM_033416.3(IMP4):c.736G>A (p.Glu246Lys)	not specified [RCV004397897]	uncertain significance	2	130346247	130346247	Human		name
405782558	CV3267524	single nucleotide variant	NM_033416.3(IMP4):c.776G>A (p.Arg259His)	not specified [RCV004397898]	uncertain significance	2	130346368	130346368	Human		name
407516276	CV3444700	single nucleotide variant	NM_033416.3(IMP4):c.476C>T (p.Thr159Ile)	not specified [RCV004628140]	uncertain significance	2	130345815	130345815	Human		name
407516284	CV3444702	single nucleotide variant	NM_033416.3(IMP4):c.697G>A (p.Val233Met)	not specified [RCV004628142]	uncertain significance	2	130346208	130346208	Human		name
407516287	CV3444703	single nucleotide variant	NM_033416.3(IMP4):c.551C>T (p.Pro184Leu)	not specified [RCV004628143]	uncertain significance	2	130345890	130345890	Human		name
407516293	CV3444705	single nucleotide variant	NM_033416.3(IMP4):c.844G>A (p.Ala282Thr)	not specified [RCV004628145]	uncertain significance	2	130346436	130346436	Human		name
407516296	CV3444706	single nucleotide variant	NM_033416.3(IMP4):c.771G>C (p.Met257Ile)	not specified [RCV004628146]	uncertain significance	2	130346363	130346363	Human		name
597775471	CV3686693	single nucleotide variant	NM_033416.3(IMP4):c.322T>A (p.Phe108Ile)	not specified [RCV004929371]	uncertain significance	2	130345582	130345582	Human		name
597775476	CV3686694	single nucleotide variant	NM_033416.3(IMP4):c.482A>G (p.Tyr161Cys)	not specified [RCV004929372]	uncertain significance	2	130345821	130345821	Human		name
597775480	CV3686695	single nucleotide variant	NM_033416.3(IMP4):c.593G>A (p.Arg198Gln)	not specified [RCV004929373]	uncertain significance	2	130345932	130345932	Human		name
597775484	CV3686696	single nucleotide variant	NM_033416.3(IMP4):c.646C>T (p.Arg216Trp)	not specified [RCV004929374]	uncertain significance	2	130346069	130346069	Human		name
597775489	CV3686697	single nucleotide variant	NM_033416.3(IMP4):c.578C>T (p.Ser193Phe)	not specified [RCV004929375]	uncertain significance	2	130345917	130345917	Human		name
598180766	CV3972417	single nucleotide variant	NM_033416.3(IMP4):c.871G>A (p.Glu291Lys)	not specified [RCV005352386]	uncertain significance	2	130346463	130346463	Human		name
598180775	CV3972418	single nucleotide variant	NM_033416.3(IMP4):c.611G>A (p.Arg204Gln)	not specified [RCV005352387]	uncertain significance	2	130346034	130346034	Human		name
8629832	CV84979	single nucleotide variant	NM_033416.1(IMP4):c.683C>T (p.Ser228Leu)	Malignant melanoma [RCV000065061]	not provided	2	130346106	130346106	Human		name

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