Eif1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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18 records found for search term Eif1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15159704	CV780142	single nucleotide variant	NM_001412.4(EIF1AX):c.101-5G>A	not provided [RCV000969759]	benign	X	20135846	20135846	Human		name
155643224	CV1706609	single nucleotide variant	NM_001412.4(EIF1AX):c.17G>T (p.Gly6Val)	See cases [RCV004584502]	uncertain significance	X	20138622	20138622	Human		name
405718459	CV3241941	single nucleotide variant	NM_005875.3(EIF1B):c.41C>G (p.Ala14Gly)	not specified [RCV004377678]	uncertain significance	3	40310902	40310902	Human		name
598178775	CV3961287	single nucleotide variant	NM_005875.3(EIF1B):c.39T>G (p.Phe13Leu)	not specified [RCV005332389]	uncertain significance	3	40310900	40310900	Human		name
597664092	CV3674355	single nucleotide variant	NM_005875.3(EIF1B):c.122G>A (p.Arg41Lys)	not specified [RCV004912257]	uncertain significance	3	40310983	40310983	Human		name
598178769	CV3961286	single nucleotide variant	NM_005875.3(EIF1B):c.257A>G (p.Gln86Arg)	not specified [RCV005332388]	uncertain significance	3	40311531	40311531	Human		name
15120878	CV717753	single nucleotide variant	NM_001412.4(EIF1AX):c.408T>C (p.Asp136=)	not provided [RCV000962793]	benign	X	20130537	20130537	Human		name
156001673	CV2257879	single nucleotide variant	NM_001412.4(EIF1AX):c.265G>A (p.Ala89Thr)	not specified [RCV004127917]	uncertain significance	X	20132254	20132254	Human		name
15173484	CV788719	single nucleotide variant	NM_001412.4(EIF1AX):c.295G>A (p.Glu99Lys)	Multiple myeloma [RCV000984125]	likely pathogenic	X	20132224	20132224	Human	2	name
156004465	CV2295942	single nucleotide variant	NM_001242481.2(EIF1AD):c.49G>A (p.Glu17Lys)	not specified [RCV004151840]	uncertain significance	11	66000341	66000341	Human		name
401768516	CV2716641	single nucleotide variant	NM_001242481.2(EIF1AD):c.173G>A (p.Arg58His)	not specified [RCV004327703]	uncertain significance	11	66000076	66000076	Human		name
407498733	CV3438062	single nucleotide variant	NM_001242481.2(EIF1AD):c.115C>T (p.His39Tyr)	not specified [RCV004622549]	uncertain significance	11	66000134	66000134	Human		name
597664075	CV3674353	single nucleotide variant	NM_001242481.2(EIF1AD):c.143G>A (p.Arg48His)	not specified [RCV004912255]	uncertain significance	11	66000106	66000106	Human		name
598178751	CV3961283	single nucleotide variant	NM_001242481.2(EIF1AD):c.145T>C (p.Phe49Leu)	not specified [RCV005332385]	uncertain significance	11	66000104	66000104	Human		name
598178757	CV3961284	single nucleotide variant	NM_001242481.2(EIF1AD):c.230G>A (p.Gly77Glu)	not specified [RCV005332386]	uncertain significance	11	65999642	65999642	Human		name
597664082	CV3674354	single nucleotide variant	NM_001242481.2(EIF1AD):c.446G>A (p.Arg149His)	not specified [RCV004912256]	uncertain significance	11	65998651	65998651	Human		name
598178745	CV3961282	single nucleotide variant	NM_001242481.2(EIF1AD):c.445C>T (p.Arg149Cys)	not specified [RCV005332384]	uncertain significance	11	65998652	65998652	Human		name
598178763	CV3961285	single nucleotide variant	NM_001242481.2(EIF1AD):c.376G>A (p.Ala126Thr)	not specified [RCV005332387]	uncertain significance	11	65998721	65998721	Human		name