Ngef Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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51 records found for search term Ngef

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8630244	CV85391	single nucleotide variant	NM_019850.2(NGEF):c.249G>A (p.Arg83=)	Malignant melanoma [RCV000065473]	not provided	2	232974642	232974642	Human		name
155927944	CV2218517	single nucleotide variant	NM_019850.3(NGEF):c.153A>C (p.Lys51Asn)	not specified [RCV004090796]	uncertain significance	2	232974738	232974738	Human		name
156299282	CV2310716	single nucleotide variant	NM_019850.3(NGEF):c.205A>G (p.Ile69Val)	not specified [RCV004157365]	likely benign	2	232974686	232974686	Human		name
156388624	CV2375939	single nucleotide variant	NM_019850.3(NGEF):c.247C>T (p.Arg83Trp)	not specified [RCV004218149]	uncertain significance	2	232974644	232974644	Human		name
156259779	CV2395502	single nucleotide variant	NM_019850.3(NGEF):c.211C>T (p.Arg71Cys)	not specified [RCV004241368]	uncertain significance	2	232974680	232974680	Human		name
401741378	CV2680394	single nucleotide variant	NM_019850.3(NGEF):c.199C>T (p.Arg67Cys)	not specified [RCV004288640]	uncertain significance	2	232974692	232974692	Human		name
405722455	CV3358681	single nucleotide variant	NM_019850.3(NGEF):c.118G>A (p.Glu40Lys)	not specified [RCV004495369]	likely benign	2	232974773	232974773	Human		name
405674871	CV3358728	single nucleotide variant	NM_019850.3(NGEF):c.200G>A (p.Arg67His)	not specified [RCV004487400]	uncertain significance	2	232974691	232974691	Human		name
597657362	CV3559213	single nucleotide variant	NM_019850.3(NGEF):c.156G>T (p.Glu52Asp)	not specified [RCV004834380]	uncertain significance	2	232974735	232974735	Human		name
15170579	CV697413	single nucleotide variant	NM_019850.3(NGEF):c.1149G>A (p.Glu383=)	not provided [RCV000949677]	benign	2	232891481	232891481	Human		name
156401182	CV2210602	single nucleotide variant	NM_019850.3(NGEF):c.426G>C (p.Glu142Asp)	not specified [RCV004083753]	uncertain significance	2	232927144	232927144	Human		name
155932215	CV2399978	single nucleotide variant	NM_019850.3(NGEF):c.890C>T (p.Ser297Phe)	not specified [RCV004246907]	uncertain significance	2	232894855	232894855	Human		name
401748853	CV2694519	single nucleotide variant	NM_019850.3(NGEF):c.590A>G (p.Gln197Arg)	not specified [RCV004298652]	uncertain significance	2	232920522	232920522	Human		name
401752328	CV2706972	single nucleotide variant	NM_019850.3(NGEF):c.619G>A (p.Gly207Arg)	not specified [RCV004321573]	uncertain significance	2	232920493	232920493	Human		name
401860680	CV2758575	single nucleotide variant	NM_019850.3(NGEF):c.562C>T (p.Leu188Phe)	not specified [RCV004337661]	uncertain significance	2	232920550	232920550	Human		name
405674983	CV3358755	single nucleotide variant	NM_019850.3(NGEF):c.421G>A (p.Glu141Lys)	not specified [RCV004487427]	uncertain significance	2	232927149	232927149	Human		name
405675047	CV3358772	single nucleotide variant	NM_019850.3(NGEF):c.605A>C (p.Glu202Ala)	not specified [RCV004487444]	uncertain significance	2	232920507	232920507	Human		name
407526939	CV3451300	single nucleotide variant	NM_019850.3(NGEF):c.609C>A (p.Asp203Glu)	not specified [RCV004654996]	uncertain significance	2	232920503	232920503	Human		name
407496983	CV3451302	single nucleotide variant	NM_019850.3(NGEF):c.599A>G (p.Glu200Gly)	not specified [RCV004643637]	uncertain significance	2	232920513	232920513	Human		name
407526943	CV3451303	single nucleotide variant	NM_019850.3(NGEF):c.333G>A (p.Met111Ile)	not specified [RCV004654997]	uncertain significance	2	232970264	232970264	Human		name
597657357	CV3559214	single nucleotide variant	NM_019850.3(NGEF):c.314A>G (p.Asn105Ser)	not specified [RCV004834381]	uncertain significance	2	232970283	232970283	Human		name
598192545	CV3997758	single nucleotide variant	NM_019850.3(NGEF):c.779G>A (p.Ser260Asn)	not specified [RCV005374369]	uncertain significance	2	232920333	232920333	Human		name
598192549	CV3997759	single nucleotide variant	NM_019850.3(NGEF):c.898A>G (p.Met300Val)	not specified [RCV005374370]	uncertain significance	2	232894847	232894847	Human		name
156250528	CV2232182	single nucleotide variant	NM_019850.3(NGEF):c.1948A>C (p.Ile650Leu)	not specified [RCV004104982]	uncertain significance	2	232879674	232879674	Human		name
156174143	CV2247652	single nucleotide variant	NM_019850.3(NGEF):c.1939G>A (p.Asp647Asn)	not specified [RCV004110983]	uncertain significance	2	232881149	232881149	Human		name
155914669	CV2264590	single nucleotide variant	NM_019850.3(NGEF):c.1497G>A (p.Met499Ile)	not specified [RCV004132602]	uncertain significance	2	232884085	232884085	Human		name
156112723	CV2267533	single nucleotide variant	NM_019850.3(NGEF):c.1099G>A (p.Val367Ile)	not specified [RCV004135953]	uncertain significance	2	232892941	232892941	Human		name
156176315	CV2317425	single nucleotide variant	NM_019850.3(NGEF):c.1259A>G (p.Lys420Arg)	not specified [RCV004172395]	uncertain significance	2	232891371	232891371	Human		name
156164663	CV2323692	single nucleotide variant	NM_019850.3(NGEF):c.1937A>T (p.Asp646Val)	not specified [RCV004165868]	uncertain significance	2	232881151	232881151	Human		name
156049181	CV2370752	single nucleotide variant	NM_019850.3(NGEF):c.1175C>T (p.Ala392Val)	not specified [RCV004209151]	uncertain significance	2	232891455	232891455	Human		name
156132405	CV2382727	single nucleotide variant	NM_019850.3(NGEF):c.2119C>T (p.Arg707Trp)	not specified [RCV004224077]	uncertain significance	2	232879503	232879503	Human		name
329353710	CV2439567	single nucleotide variant	NM_019850.3(NGEF):c.1174G>A (p.Ala392Thr)	not specified [RCV004255590]	uncertain significance	2	232891456	232891456	Human		name
329379614	CV2456354	single nucleotide variant	NM_019850.3(NGEF):c.1054G>A (p.Val352Met)	not specified [RCV004275519]	uncertain significance	2	232892986	232892986	Human		name
401759613	CV2687388	single nucleotide variant	NM_019850.3(NGEF):c.1376G>A (p.Arg459Lys)	not specified [RCV004300639]	uncertain significance	2	232885341	232885341	Human		name
401725647	CV2697498	single nucleotide variant	NM_019850.3(NGEF):c.1312T>C (p.Cys438Arg)	not specified [RCV004297887]	uncertain significance	2	232888068	232888068	Human		name
401865329	CV2754224	single nucleotide variant	NM_019850.3(NGEF):c.1163G>C (p.Arg388Pro)	not specified [RCV004334412]	uncertain significance	2	232891467	232891467	Human		name
401862563	CV2762220	single nucleotide variant	NM_019850.3(NGEF):c.1957G>A (p.Glu653Lys)	not specified [RCV004335347]	uncertain significance	2	232879665	232879665	Human		name
401858384	CV2774060	single nucleotide variant	NM_019850.3(NGEF):c.2110C>A (p.Leu704Met)	not specified [RCV004345662]	uncertain significance	2	232879512	232879512	Human		name
405674739	CV3358693	single nucleotide variant	NM_019850.3(NGEF):c.1339C>G (p.Leu447Val)	not specified [RCV004487365]	uncertain significance	2	232888041	232888041	Human		name
405674770	CV3358701	single nucleotide variant	NM_019850.3(NGEF):c.1415A>G (p.Lys472Arg)	not specified [RCV004487373]	uncertain significance	2	232885302	232885302	Human		name
405674794	CV3358708	single nucleotide variant	NM_019850.3(NGEF):c.1631C>T (p.Pro544Leu)	not specified [RCV004487380]	uncertain significance	2	232883437	232883437	Human		name
405674848	CV3358722	single nucleotide variant	NM_019850.3(NGEF):c.1979G>A (p.Arg660Lys)	not specified [RCV004487394]	uncertain significance	2	232879643	232879643	Human		name
405674880	CV3358730	single nucleotide variant	NM_019850.3(NGEF):c.2057G>A (p.Arg686His)	not specified [RCV004487402]	uncertain significance	2	232879565	232879565	Human		name
405674900	CV3358736	single nucleotide variant	NM_019850.3(NGEF):c.2062C>T (p.His688Tyr)	not specified [RCV004487408]	uncertain significance	2	232879560	232879560	Human		name
407526936	CV3451299	single nucleotide variant	NM_019850.3(NGEF):c.1943G>A (p.Gly648Glu)	not specified [RCV004654995]	uncertain significance	2	232879679	232879679	Human		name
407496979	CV3451301	single nucleotide variant	NM_019850.3(NGEF):c.1007A>G (p.Glu336Gly)	not specified [RCV004643636]	uncertain significance	2	232893033	232893033	Human		name
597657370	CV3559212	single nucleotide variant	NM_019850.3(NGEF):c.1430A>C (p.Lys477Thr)	not specified [RCV004834379]	uncertain significance	2	232885287	232885287	Human		name
598192533	CV3997756	single nucleotide variant	NM_019850.3(NGEF):c.1112C>T (p.Thr371Ile)	not specified [RCV005374367]	uncertain significance	2	232892928	232892928	Human		name
598192539	CV3997757	single nucleotide variant	NM_019850.3(NGEF):c.1217C>T (p.Ser406Phe)	not specified [RCV005374368]	uncertain significance	2	232891413	232891413	Human		name
598192555	CV3997760	single nucleotide variant	NM_019850.3(NGEF):c.1570G>A (p.Asp524Asn)	not specified [RCV005374371]	uncertain significance	2	232884012	232884012	Human		name
8630243	CV85390	single nucleotide variant	NM_001114090.1(NGEF):c.624G>A (p.Met208Ile)	Malignant melanoma [RCV000065472]	not provided	2	232894845	232894845	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
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