C1qtnf9 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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78 records found for search term C1qtnf9

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401722714	CV2703473	single nucleotide variant	NM_178540.5(C1QTNF9):c.65C>A (p.Thr22Asn)	not specified [RCV004317659]	uncertain significance	13	24316068	24316068	Human		name
155931928	CV2221121	single nucleotide variant	NM_178540.5(C1QTNF9):c.111T>A (p.Asn37Lys)	not specified [RCV004094573]	uncertain significance	13	24316114	24316114	Human		name
156015862	CV2298993	single nucleotide variant	NM_178540.5(C1QTNF9):c.139G>A (p.Gly47Arg)	not specified [RCV004158518]	uncertain significance	13	24316142	24316142	Human		name
156097346	CV2310261	single nucleotide variant	NM_178540.5(C1QTNF9):c.143C>T (p.Ala48Val)	not specified [RCV004157011]	uncertain significance	13	24316146	24316146	Human		name
156092147	CV2384886	single nucleotide variant	NM_178540.5(C1QTNF9):c.108C>G (p.His36Gln)	not specified [RCV004225761]	uncertain significance	13	24316111	24316111	Human		name
329362537	CV2438844	single nucleotide variant	NM_178540.5(C1QTNF9):c.160G>A (p.Asp54Asn)	not specified [RCV004264379]	uncertain significance	13	24316163	24316163	Human		name
401768508	CV2675393	single nucleotide variant	NM_178540.5(C1QTNF9):c.125G>T (p.Arg42Ile)	not specified [RCV004292196]	uncertain significance	13	24316128	24316128	Human		name
401759824	CV2701737	single nucleotide variant	NM_178540.5(C1QTNF9):c.110A>G (p.Asn37Ser)	not specified [RCV004314141]	uncertain significance	13	24316113	24316113	Human		name
407496153	CV3418141	single nucleotide variant	NM_178540.5(C1QTNF9):c.223G>A (p.Glu75Lys)	not specified [RCV004605913]	uncertain significance	13	24318874	24318874	Human		name
597750235	CV3643852	single nucleotide variant	NM_178540.5(C1QTNF9):c.282A>C (p.Arg94Ser)	not specified [RCV004892517]	uncertain significance	13	24321048	24321048	Human		name
597793274	CV3643853	single nucleotide variant	NM_178540.5(C1QTNF9):c.169G>A (p.Glu57Lys)	not specified [RCV004902927]	uncertain significance	13	24318820	24318820	Human		name
598187929	CV3950070	single nucleotide variant	NM_178540.5(C1QTNF9):c.173C>G (p.Pro58Arg)	not specified [RCV005312106]	uncertain significance	13	24318824	24318824	Human		name
156401733	CV2217610	single nucleotide variant	NM_178540.5(C1QTNF9):c.868G>A (p.Gly290Ser)	not specified [RCV004090132]	uncertain significance	13	24321634	24321634	Human		name
156066581	CV2236922	single nucleotide variant	NM_178540.5(C1QTNF9):c.688G>A (p.Glu230Lys)	not specified [RCV004112925]	uncertain significance	13	24321454	24321454	Human		name
156058932	CV2262938	single nucleotide variant	NM_178540.5(C1QTNF9):c.991A>G (p.Ser331Gly)	not specified [RCV004125076]	uncertain significance	13	24321757	24321757	Human		name
156204347	CV2300806	single nucleotide variant	NM_178540.5(C1QTNF9):c.616G>T (p.Val206Leu)	not specified [RCV004157737]	uncertain significance	13	24321382	24321382	Human		name
156275730	CV2318366	single nucleotide variant	NM_178540.5(C1QTNF9):c.784G>C (p.Val262Leu)	not specified [RCV004179526]	uncertain significance	13	24321550	24321550	Human		name
156294888	CV2321451	single nucleotide variant	NM_178540.5(C1QTNF9):c.304C>T (p.Pro102Ser)	not specified [RCV004177429]	uncertain significance	13	24321070	24321070	Human		name
155917048	CV2366815	single nucleotide variant	NM_178540.5(C1QTNF9):c.725C>T (p.Thr242Met)	not specified [RCV004210805]	uncertain significance	13	24321491	24321491	Human		name
156259580	CV2380998	single nucleotide variant	NM_178540.5(C1QTNF9):c.516G>C (p.Gln172His)	not specified [RCV004225040]	uncertain significance	13	24321282	24321282	Human		name
156181984	CV2384122	single nucleotide variant	NM_178540.5(C1QTNF9):c.506C>T (p.Thr169Met)	not specified [RCV004227526]	likely benign	13	24321272	24321272	Human		name
156093526	CV2389710	single nucleotide variant	NM_178540.5(C1QTNF9):c.730C>T (p.His244Tyr)	not specified [RCV004243759]	uncertain significance	13	24321496	24321496	Human		name
155960616	CV2390723	single nucleotide variant	NM_178540.5(C1QTNF9):c.995G>A (p.Ser332Asn)	not specified [RCV004241020]	uncertain significance	13	24321761	24321761	Human		name
329386827	CV2439426	single nucleotide variant	NM_178540.5(C1QTNF9):c.532C>T (p.Arg178Trp)	not specified [RCV004249716]	uncertain significance	13	24321298	24321298	Human		name
401718246	CV2700261	single nucleotide variant	NM_178540.5(C1QTNF9):c.580G>A (p.Gly194Ser)	not specified [RCV004310927]	uncertain significance	13	24321346	24321346	Human		name
401781261	CV2726476	single nucleotide variant	NM_178540.5(C1QTNF9):c.590T>C (p.Leu197Pro)	not specified [RCV004328665]	likely benign	13	24321356	24321356	Human		name
401872046	CV2754248	single nucleotide variant	NM_178540.5(C1QTNF9):c.452C>T (p.Pro151Leu)	not specified [RCV004334434]	uncertain significance	13	24321218	24321218	Human		name
405733060	CV3295059	single nucleotide variant	NM_178540.5(C1QTNF9):c.388G>A (p.Val130Met)	not specified [RCV004429604]	uncertain significance	13	24321154	24321154	Human		name
405733069	CV3295060	single nucleotide variant	NM_178540.5(C1QTNF9):c.967A>G (p.Thr323Ala)	not specified [RCV004429605]	uncertain significance	13	24321733	24321733	Human		name
407496159	CV3418139	single nucleotide variant	NM_178540.5(C1QTNF9):c.922G>A (p.Gly308Arg)	not specified [RCV004605911]	uncertain significance	13	24321688	24321688	Human		name
597750228	CV3643851	single nucleotide variant	NM_178540.5(C1QTNF9):c.580G>C (p.Gly194Arg)	not specified [RCV004892516]	uncertain significance	13	24321346	24321346	Human		name
598187910	CV3950066	single nucleotide variant	NM_178540.5(C1QTNF9):c.949G>T (p.Asp317Tyr)	not specified [RCV005312103]	uncertain significance	13	24321715	24321715	Human		name
598211558	CV3950067	single nucleotide variant	NM_178540.5(C1QTNF9):c.746A>G (p.Tyr249Cys)	not specified [RCV005316032]	uncertain significance	13	24321512	24321512	Human		name
598187917	CV3950068	single nucleotide variant	NM_178540.5(C1QTNF9):c.829A>G (p.Lys277Glu)	not specified [RCV005312104]	uncertain significance	13	24321595	24321595	Human		name
598187923	CV3950069	single nucleotide variant	NM_178540.5(C1QTNF9):c.790G>T (p.Val264Leu)	not specified [RCV005312105]	uncertain significance	13	24321556	24321556	Human		name
598187935	CV3950071	single nucleotide variant	NM_178540.5(C1QTNF9):c.554G>C (p.Gly185Ala)	not specified [RCV005312107]	uncertain significance	13	24321320	24321320	Human		name
405733087	CV3295062	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.4A>T (p.Arg2Trp)	not specified [RCV004429607]	uncertain significance	13	23896983	23896983	Human		name
401910092	CV2813768	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.204G>T (p.Gly68=)	not provided [RCV003398337]	likely benign	13	23894164	23894164	Human		name
156128793	CV2358521	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.83C>G (p.Pro28Arg)	not specified [RCV004207405]	uncertain significance	13	23896904	23896904	Human		name
405733107	CV3295065	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.76G>A (p.Gly26Arg)	not specified [RCV004429610]	uncertain significance	13	23896911	23896911	Human		name
407496148	CV3418142	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.81C>A (p.His27Gln)	not specified [RCV004605914]	uncertain significance	13	23896906	23896906	Human		name
407496145	CV3418143	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.86G>C (p.Gly29Ala)	not specified [RCV004605915]	uncertain significance	13	23896901	23896901	Human		name
597750241	CV3643855	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.94G>A (p.Gly32Arg)	not specified [RCV004892518]	uncertain significance	13	23896893	23896893	Human		name
598211564	CV3950072	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.62A>G (p.Asp21Gly)	not specified [RCV005316033]	uncertain significance	13	23896925	23896925	Human		name
15162175	CV725427	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.957C>T (p.Asp319=)	not provided [RCV000881709]	benign	13	23891334	23891334	Human		name
156378019	CV2207613	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.158G>A (p.Gly53Asp)	not specified [RCV004090395]	uncertain significance	13	23896829	23896829	Human		name
156104542	CV2260583	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.169G>A (p.Glu57Lys)	not specified [RCV004123353]	uncertain significance	13	23894199	23894199	Human		name
156048474	CV2319240	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.104G>A (p.Gly35Asp)	not specified [RCV004178285]	uncertain significance	13	23896883	23896883	Human		name
156083005	CV2368966	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.143C>A (p.Ala48Glu)	not specified [RCV004207912]	uncertain significance	13	23896844	23896844	Human		name
156036795	CV2374015	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.103G>A (p.Gly35Ser)	not specified [RCV004227142]	likely benign	13	23896884	23896884	Human		name
155928977	CV2389033	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.113G>T (p.Gly38Val)	not specified [RCV004242024]	uncertain significance	13	23896874	23896874	Human		name
401757584	CV2675394	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.125G>T (p.Arg42Ile)	not specified [RCV004292197]	uncertain significance	13	23896862	23896862	Human		name
401858538	CV2774340	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.154A>C (p.Lys52Gln)	not specified [RCV004347692]	uncertain significance	13	23896833	23896833	Human		name
597793285	CV3643857	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.134G>A (p.Arg45Gln)	not specified [RCV004902930]	uncertain significance	13	23896853	23896853	Human		name
597793293	CV3643861	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.110A>G (p.Asn37Ser)	not specified [RCV004902933]	uncertain significance	13	23896877	23896877	Human		name
156161474	CV2311742	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.904T>G (p.Trp302Gly)	not specified [RCV004170609]	uncertain significance	13	23891387	23891387	Human		name
156391877	CV2382696	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.841G>A (p.Val281Met)	not specified [RCV004233009]	likely benign	13	23891450	23891450	Human		name
329354899	CV2449162	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.868A>G (p.Ser290Gly)	not specified [RCV004264220]	likely benign	13	23891423	23891423	Human		name
329394238	CV2450197	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.958G>A (p.Asp320Asn)	not specified [RCV004271014]	uncertain significance	13	23891333	23891333	Human		name
329360790	CV2462988	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.941T>C (p.Leu314Ser)	not specified [RCV004272820]	uncertain significance	13	23891350	23891350	Human		name
401732561	CV2691043	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.957C>A (p.Asp319Glu)	not specified [RCV004301051]	uncertain significance	13	23891334	23891334	Human		name
401758513	CV2694140	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.791T>A (p.Val264Glu)	not specified [RCV004302569]	uncertain significance	13	23891500	23891500	Human		name
405733079	CV3295061	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.347G>A (p.Gly116Glu)	not specified [RCV004429606]	uncertain significance	13	23891944	23891944	Human		name
405733093	CV3295063	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.589C>G (p.Leu197Val)	not specified [RCV004429608]	uncertain significance	13	23891702	23891702	Human		name
405733100	CV3295064	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.746A>G (p.Tyr249Cys)	not specified [RCV004429609]	uncertain significance	13	23891545	23891545	Human		name
405733115	CV3295066	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.872T>G (p.Ile291Ser)	not specified [RCV004429611]	uncertain significance	13	23891419	23891419	Human		name
405733123	CV3295067	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.935A>G (p.Asn312Ser)	not specified [RCV004429612]	uncertain significance	13	23891356	23891356	Human		name
407496142	CV3418144	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.929G>A (p.Arg310Lys)	not specified [RCV004605916]	uncertain significance	13	23891362	23891362	Human		name
597793277	CV3643854	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.532C>T (p.Arg178Trp)	not specified [RCV004902928]	uncertain significance	13	23891759	23891759	Human		name
597793282	CV3643856	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.426T>G (p.Ile142Met)	not specified [RCV004902929]	uncertain significance	13	23891865	23891865	Human		name
597793287	CV3643858	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.910C>A (p.Gln304Lys)	not specified [RCV004902931]	uncertain significance	13	23891381	23891381	Human		name
597750246	CV3643860	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.511C>A (p.Pro171Thr)	not specified [RCV004892519]	uncertain significance	13	23891780	23891780	Human		name
597793297	CV3643862	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.979T>C (p.Phe327Leu)	not specified [RCV004902934]	uncertain significance	13	23891312	23891312	Human		name
598187941	CV3950073	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.436G>A (p.Gly146Ser)	not specified [RCV005312108]	uncertain significance	13	23891855	23891855	Human		name
598187947	CV3950074	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.860C>A (p.Ala287Asp)	not specified [RCV005312109]	uncertain significance	13	23891431	23891431	Human		name
598187955	CV3950075	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.796T>G (p.Leu266Val)	not specified [RCV005312110]	uncertain significance	13	23891495	23891495	Human		name
15193748	CV702633	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.727T>A (p.Cys243Ser)	not provided [RCV000955460]	benign	13	23891564	23891564	Human		name
15171946	CV713883	single nucleotide variant	NM_001007537.3(C1QTNF9B):c.830G>A (p.Arg277Lys)	not provided [RCV000972302]	benign	13	23891461	23891461	Human		name

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