Gabrp Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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44 records found for search term Gabrp

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155964586	CV2282858	single nucleotide variant	NM_014211.3(GABRP):c.65A>G (p.Gln22Arg)	not specified [RCV004143512]	uncertain significance	5	170789140	170789140	Human		name
401742611	CV2677636	single nucleotide variant	NM_014211.3(GABRP):c.91G>A (p.Gly31Ser)	not specified [RCV004291727]	likely benign	5	170789166	170789166	Human		name
405732567	CV3254169	single nucleotide variant	NM_014211.3(GABRP):c.58T>C (p.Cys20Arg)	not specified [RCV004390176]	uncertain significance	5	170789133	170789133	Human		name
597743644	CV3673338	single nucleotide variant	NM_014211.3(GABRP):c.32G>T (p.Cys11Phe)	not specified [RCV004922091]	uncertain significance	5	170788647	170788647	Human		name
156183206	CV2222363	single nucleotide variant	NM_014211.3(GABRP):c.197C>G (p.Thr66Ser)	not specified [RCV004099232]	uncertain significance	5	170794255	170794255	Human		name
11638005	CV266053	deletion	NM_014211.3(GABRP):c.607del (p.Glu203fs)	not provided [RCV000295694]	uncertain significance	5	170805780	170805780	Human		name
401733283	CV2685480	single nucleotide variant	NM_014211.3(GABRP):c.115C>A (p.Pro39Thr)	not specified [RCV004294503]	uncertain significance	5	170789190	170789190	Human		name
407486265	CV3439595	single nucleotide variant	NM_014211.3(GABRP):c.127A>G (p.Asn43Asp)	not specified [RCV004619064]	uncertain significance	5	170789202	170789202	Human		name
597743628	CV3673333	single nucleotide variant	NM_014211.3(GABRP):c.136G>A (p.Ala46Thr)	not specified [RCV004922088]	uncertain significance	5	170789211	170789211	Human		name
597743650	CV3673339	single nucleotide variant	NM_014211.3(GABRP):c.216C>G (p.Ile72Met)	not specified [RCV004922092]	uncertain significance	5	170794274	170794274	Human		name
155973214	CV2210997	single nucleotide variant	NM_014211.3(GABRP):c.617G>A (p.Arg206Gln)	not specified [RCV004088194]	uncertain significance	5	170805791	170805791	Human		name
155917125	CV2236472	single nucleotide variant	NM_014211.3(GABRP):c.675G>C (p.Glu225Asp)	not specified [RCV004110476]	uncertain significance	5	170805849	170805849	Human		name
155921031	CV2240460	single nucleotide variant	NM_014211.3(GABRP):c.407G>A (p.Gly136Glu)	not specified [RCV004117343]	uncertain significance	5	170795374	170795374	Human		name
156272684	CV2247487	single nucleotide variant	NM_014211.3(GABRP):c.484A>G (p.Met162Val)	not specified [RCV004108810]	uncertain significance	5	170797491	170797491	Human		name
156348121	CV2312615	single nucleotide variant	NM_014211.3(GABRP):c.440C>T (p.Thr147Met)	not specified [RCV004169353]	uncertain significance	5	170795407	170795407	Human		name
155989977	CV2374589	single nucleotide variant	NM_014211.3(GABRP):c.616C>T (p.Arg206Trp)	not specified [RCV004225215]	uncertain significance	5	170805790	170805790	Human		name
156051420	CV2386328	single nucleotide variant	NM_014211.3(GABRP):c.421C>T (p.Arg141Cys)	not specified [RCV004228670]	uncertain significance	5	170795388	170795388	Human		name
156101098	CV2392997	single nucleotide variant	NM_014211.3(GABRP):c.716G>A (p.Arg239Gln)	not specified [RCV004242850]	uncertain significance	5	170808636	170808636	Human		name
329400566	CV2438497	single nucleotide variant	NM_014211.3(GABRP):c.482A>G (p.Asn161Ser)	not specified [RCV004259643]	uncertain significance	5	170797489	170797489	Human		name
329379922	CV2456560	single nucleotide variant	NM_014211.3(GABRP):c.429C>G (p.Phe143Leu)	not specified [RCV004277485]	uncertain significance	5	170795396	170795396	Human		name
329364099	CV2469748	single nucleotide variant	NM_014211.3(GABRP):c.751G>A (p.Val251Ile)	not specified [RCV004284943]	uncertain significance	5	170808671	170808671	Human		name
401760071	CV2694912	single nucleotide variant	NM_014211.3(GABRP):c.309G>C (p.Lys103Asn)	not specified [RCV004301303]	uncertain significance	5	170795276	170795276	Human		name
401888087	CV2791234	single nucleotide variant	NM_014211.3(GABRP):c.776T>C (p.Leu259Ser)	not specified [RCV004356871]	uncertain significance	5	170808696	170808696	Human		name
405732544	CV3254166	single nucleotide variant	NM_014211.3(GABRP):c.386T>C (p.Phe129Ser)	not specified [RCV004390173]	uncertain significance	5	170795353	170795353	Human		name
405732562	CV3254168	single nucleotide variant	NM_014211.3(GABRP):c.445C>A (p.Leu149Met)	not specified [RCV004390175]	uncertain significance	5	170795412	170795412	Human		name
597743616	CV3673331	single nucleotide variant	NM_014211.3(GABRP):c.749A>G (p.Tyr250Cys)	not specified [RCV004922086]	uncertain significance	5	170808669	170808669	Human		name
597743622	CV3673332	single nucleotide variant	NM_014211.3(GABRP):c.784G>A (p.Val262Ile)	not specified [RCV004922087]	uncertain significance	5	170808704	170808704	Human		name
597779463	CV3673334	single nucleotide variant	NM_014211.3(GABRP):c.329G>A (p.Arg110His)	not specified [RCV004930384]	uncertain significance	5	170795296	170795296	Human		name
597779466	CV3673335	single nucleotide variant	NM_014211.3(GABRP):c.797T>A (p.Ile266Asn)	not specified [RCV004930385]	uncertain significance	5	170808717	170808717	Human		name
597743634	CV3673336	single nucleotide variant	NM_014211.3(GABRP):c.702A>T (p.Leu234Phe)	not specified [RCV004922089]	uncertain significance	5	170808622	170808622	Human		name
598245364	CV3977447	single nucleotide variant	NM_014211.3(GABRP):c.577C>G (p.Leu193Val)	not specified [RCV005345004]	uncertain significance	5	170805751	170805751	Human		name
598245372	CV3977448	single nucleotide variant	NM_014211.3(GABRP):c.452C>A (p.Ala151Asp)	not specified [RCV005345005]	uncertain significance	5	170795419	170795419	Human		name
598158776	CV3977449	single nucleotide variant	NM_014211.3(GABRP):c.715C>T (p.Arg239Trp)	not specified [RCV005328127]	uncertain significance	5	170808635	170808635	Human		name
15145335	CV709824	single nucleotide variant	NM_014211.3(GABRP):c.599G>A (p.Arg200His)	not provided [RCV000966979]	benign	5	170805773	170805773	Human		name
8631546	CV86750	single nucleotide variant	NM_014211.2(GABRP):c.680G>A (p.Gly227Glu)	Malignant melanoma [RCV000066841]	not provided	5	170808600	170808600	Human		name
8631547	CV86751	single nucleotide variant	NM_014211.2(GABRP):c.805G>A (p.Asp269Asn)	Malignant melanoma [RCV000066842]	not provided	5	170808725	170808725	Human		name
156388276	CV2231755	single nucleotide variant	NM_014211.3(GABRP):c.1273A>C (p.Ile425Leu)	not specified [RCV004098571]	uncertain significance	5	170812208	170812208	Human		name
156139972	CV2250640	single nucleotide variant	NM_014211.3(GABRP):c.1192A>G (p.Lys398Glu)	not specified [RCV004129273]	uncertain significance	5	170812127	170812127	Human		name
156339619	CV2271442	single nucleotide variant	NM_014211.3(GABRP):c.1211A>T (p.Asp404Val)	not specified [RCV004136545]	uncertain significance	5	170812146	170812146	Human		name
156279326	CV2338302	single nucleotide variant	NM_014211.3(GABRP):c.1049G>A (p.Ser350Asn)	not specified [RCV004186357]	likely benign	5	170811984	170811984	Human		name
401752498	CV2707029	single nucleotide variant	NM_014211.3(GABRP):c.1040A>G (p.Glu347Gly)	not specified [RCV004321622]	uncertain significance	5	170811975	170811975	Human		name
401915436	CV2825563	single nucleotide variant	NM_014211.3(GABRP):c.1046T>C (p.Val349Ala)	not provided [RCV003428715]	likely benign	5	170811981	170811981	Human		name
404979533	CV2850140	single nucleotide variant	NM_014211.3(GABRP):c.1126G>A (p.Asp376Asn)	not provided [RCV003487853]\|not specified [RCV004364881]	uncertain significance	5	170812061	170812061	Human		name
15140391	CV735003	single nucleotide variant	NM_014211.3(GABRP):c.1028C>T (p.Thr343Ile)	not provided [RCV000899311]	likely benign	5	170811963	170811963	Human		name

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